Lediga jobb som Naturvetenskapligt arbete i Mölndal

Job description
Senior Scientist in Process Analytical Technology (PAT) - Make a Meaningful Impact on People's Lives!
Are you ready to take your career to the next level and make a meaningful impact on people's lives with life-changing medicines? Join our Operations team in Gothenburg as a Senior Scientist and be part of a team where everyone feels a personal connection to the people we impact.
At AstraZeneca, our Operations team has a big ambition: to deliver more medicines to patients, quicker and more affordably. We are driven by our commitment to deliver accelerated growth for AstraZeneca and to make people's lives better.
In Pharmaceutical Technology and Development (PT&D), within Operations, we are the bridge between brilliant science and innovative medicines that help millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.
At Global Product Development (GPD) in Gothenburg, a sub-division of PT&D, we focus on the fields of Oral Controlled Release Drug products and Immediate Release Drug Products. You will join a vibrant team that is working on the next generation of medicines and play a key role in the development of new medicinal products.
We are currently looking for a Senior Scientist for PAT in our Product and Process Control group to strengthen our capabilities in the development and implementation of enhanced control strategies using the newest technologies to our late phase portfolio. If you have a solid scientific foundation in this domain and the aspiration to grow into an expert, this role offers an excellent fit.
This is a consultant assignment with Randstad Life Sciences starting in February. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.


Deadline 2026-01-12 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Responsibilities
As a Senior Scientist, you will design, develop, and deliver high?quality enhanced control methods by applying expertise in Process Analytical Technology (PAT), chemometrics, and advanced process monitoring and control. Hands?on laboratory work will be a core part of your role.
You will collaborate with cross?functional project teams, contribute to regulatory documentation, and support digital initiatives that implement innovative monitoring and control tools across continuous manufacturing platforms.
You will participate in the development, validation and technical transfer of methods and PAT tools to enable robust product control strategies across Operations. You will also champion a future?focused, innovative mindset, advancing data science, predictive modelling and simulation, and artificial intelligence to drive digitally oriented approaches.

Qualifications
Essential for the role:
BSc, MSc or equivalent in a relevant discipline (chemistry, pharmacy, engineering etc.) with experience in the use of PAT in the Pharmaceutical or Chemical industries and/or postgraduate experience in Academia with a PAT industrial focus.
A strong understanding of key PAT (e.g., NIR, Raman and microwave spectroscopy)
PAT method development experience, implementation and use of multi-variate data analysis/ Chemometrics (MVDA, PCA, PLS) in common software platforms (SIMCA, Python, MATLAB, PLS Toolbox etc.)
Ability to document and present your work concisely and comprehensibly
Strong collaboration, communication, and leadership skills
An understanding of the principles and management of Safety, Health & Environment (SHE)

Desirable for the role:
Demonstrated experience of ensuring compliance with operational requirements (GMP, GAMP, Process Safety, Data integrity, Change Control)
Experience of developing control strategies for pharmaceutical commercial manufacturing processes
Basic scripting skills (e.g. Python, Matlab, R)
Experience with digital tools supporting enhanced control strategies (DCS, PAT management system, APC, Multivariate monitoring platform)
Knowledge of pharmaceutical process equipment/technology for continuous processes


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.
With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Fladdermusinventerare till Jakobi Sustainability AB
Om tjänsten
Jakobi Sustainability söker nu en fladdermusinventerare som vill arbeta med fältinventeringar, ljudanalys och rapportskrivning inom ramen för miljöbedömningar och tillståndsprocesser. Rollen är en viktig del av våra uppdrag kopplade till exploateringsprojekt, artskyddsfrågor och MKB-arbete, där fladdermöss ofta är en central artgrupp.
Vi söker dig som redan har erfarenhet av fladdermusarbete och som vill utvecklas vidare i en konsultroll.
För att stärka vår geografiska täckning ser vi gärna att du är placerad i Luleå, Uppsala eller Göteborg.
Hos oss får du arbeta i ett engagerat och kunnigt team, med korta beslutsvägar och stor möjlighet att påverka både din roll och utvecklingen av Jakobis fladdermusverksamhet.


Dina arbetsuppgifter
Planera och genomföra fältinventeringar av fladdermöss
Arbeta med ljudanalys i program som t.ex. Batsound eller Kaleidoscope
Skriva rapporter och underlag till MKB och artskyddsutredningar
Delta i förstudier och metodval kopplade till fladdermusutredningar
Vara ett stöd till kollegor och kunder i frågor som rör fladdermöss och artskydd
Kundkontakt och offertskrivning



Arbetet innebär nattarbete under inventeringssäsong samt resor inom hela Sverige.


Vi söker dig som har:
Erfarenhet av fladdermusinventering i fält
Erfarenhet av ljudanalys och rapportskrivning
Kandidatexamen inom biologi, ekologi eller annan relevant naturvetenskaplig utbildning
God förmåga att arbeta självständigt och strukturerat
Mycket goda kunskaper i svenska i tal och skrift
B-körkort



Meriterande
Erfarenhet av arbete som ekolog eller miljökonsult
Kunskap om artskyddslagstiftning kopplat till fladdermöss
Erfarenhet av GIS
Erfarenhet av arbete med autoboxar och ultraljudsdetektorer
Erfarenhet inom andra artgrupper (t.ex. fåglar) eller naturvärdesinventeringar enlig svensk standard



Som person är du
Kommunikativ och samarbetsinriktad
Självständig och ansvarstagande
Noggrann och analytisk
Bekväm med att arbeta nattetid och ute i fält



Vi erbjuder
Möjlighet att arbeta i en växande och specialistdriven verksamhet
Stor frihet under ansvar och möjlighet till hemarbete
Ett företag som värdesätter kvalitet, engagemang och långsiktiga relationer
Kollektivavtal och goda villkor



Placeringsort
För att stärka vår geografiska täckning ser vi gärna att du är placerad i Luleå, Uppsala eller Göteborg. Annan placering kan diskuteras. Vi har kontor i Uppsala, Kalmar, Luleå och Jönköping med huvudkontor i Göteborg.
Ansökan
Mejla eventuella frågor samt din ansökan (cv samt personligt brev) [email protected]. Intervjuer sker löpande. Frågor kan även besvaras av Julius Stölzle (Ansvarig för kompetensområde fladdermöss, mail:[email protected]?tel.:?0703 09 79 86) eller Linda Hassel (Affärsområdeschef naturmiljö; mail: [email protected], tel.: 072-500 11 27).
Välkommen med din ansökan! Visa mindre

Vi söker nu en engagerad och noggrann medarbetare med intresse för kvalité. Du kommer vara en del i ett litet team vars främsta uppgift att utföra kvalitetskontroll och prestandautvärdering. Delta i designförändringar och utredningar för att upprätthålla kvalité och leveranssäkerhet hos våra produkter.
Tjänsten
Dina huvudsakliga arbetsuppgifter blir att utföra kvalitetskontroll och uppföljning av produktprestanda samt att på sikt delta i utredningar gällande avvikande material och eventuella designförändringar.
Tjänsten innefattar även visst underhåll och skötsel av utrustning, samt dokumentation i styrda batchprotokoll och rapportering i enlighet med vårt kvalitetssystem.
Din bakgrund och kvalifikationer:
MSc. i bioteknik, biokemi, molekylärbiologi eller med liknande inriktning. 
erfarenhet av laboratoriearbete. 
goda kunskaper i matematik och dataanalys.
utmärkta kommunikationsfärdigheter i svenska och engelska, i både tal och skrift.

Meriterande erfarenheter:
erfarenhet av Immunoassays och IVD-produkter, gärna inom kvalitetskontroll. 
arbetat med EIA/ELISA tekniker. 
arbetat enligt Kvalitetsledningssystem, gärna ISO13485.

Vem är du?
Vi söker dig som med engagemang och noggrannhet tar dig an dina arbetsuppgifter. Vi värdesätter förmåga att lösa problem på ett konstruktivt sätt och att samarbeta med andra – tillsammans skapar vi en bra arbetsmiljö och når våra gemensamma mål.
För att trivas och lyckas i rollen är det viktigt att du har en positiv inställning till din omgivning. Är du dessutom kvalitetsmedveten och strukturerad med förmåga att hålla tider i en verksamhet med många deadlines, kan jobba självständigt och i grupp, så är det din profil vi söker.
Arbetsplats och kultur
Hos oss på Fujirebio hittar du en härlig gemenskap där vi jobbar tillsammans i en engagerande och dynamisk miljö för att leverera produkter som svarar mot kundernas förväntan, myndigheternas krav samt inte minst patienternas behov.
Anställning
Tillträde: 1 januari eller enligt överenskommelse. Anställningen är en tillsvidareanställning med en omfattning på 100 % dagtid.
Vill du veta mer?
Har du frågor om tjänsten, är du välkommen att kontakta rekryterande chef Maria Lundin, [email protected] 
Välkommen med din ansökan! Skicka in din ansökan senast 8 december. Visa mindre

About the Role
We are looking for someone interested in working on separation membrane development at the startup Retein AB. You will be part of a multidisciplinary team in a small, but growing company, where each day is varied with respect to the tasks at hand. Together, we develop filters for efficient circular use of waterborne resources across a wide range of industries.
At Retein, we are passionate about closing the loop on resources such as clean water, metals, and nutrients in order to enable long-term sustainable manufacturing and use of natural resources.
Desired Skills
We seek someone with:
Prior experience in separation membrane development and membrane performance evaluation in a lab environment.
Prior experience with formulating polymers for membrane applications.
Knowledge and experience with material characterization tools such as microscopy and particle size analysis.
Prior experience from protein handling in a lab environment is preferrable.
Prior experience from waste to value initiatives is preferrable.
The desire to work closely with other members of a team, but who is also capable to perform on their own. Visa mindre

Regulatory Associate
As part of our mission to make the shipping industry more sustainable, we are expanding our Regulatory Affairs team.
We are looking for a Regulatory Associate to strengthen our Regulatory Affairs team and support the growth of Selektope, working closely with our Director of Regulatory Affairs and Sustainability.
Why join I-Tech?
At I-Tech, we keep marine sustainability close to heart and our vision is to shape the future of biofouling prevention through science. As the developers behind Selektope—a unique biotechnology that prevents barnacle growth on ship hulls—we help the shipping industry reduce fuel consumption, emissions and invasive species.
Headquartered in GoCo Health Innovation City in Mölndal, we’re a tight, diverse and driven team working at the intersection of innovation and impact. Listed on Nasdaq First North, I-Tech is a growing company where you will join a team that values transparency, integrity, and the contributions of every individual.
Key Responsibilities:
Support global regulatory implementation and maintenance
Take on increasing responsibility for registrations and notifications for Selektope
Conduct feasibility studies for new regulatory projects
Author safety data sheets and classify chemicals

Were looking for someone with:
MSc in Chemistry, Biology, Toxicology, Chemical Engineering or similar
Approximately 5 years of  experience fo regulatory affairs regarding chemicals, biocides, or pharmaceuticals
Experience in hazard/risk assessment and SDS authoring
Self-driven, detail-oriented, and solution-focused personality
Strong communication skills; fluent in English

I-Tech offers:
a fast-paced, entrepreneurial environment
a diverse team passionate about ocean sustainability
Enjoy flexibility, impact, and a competitive compensation package

Other information:
Location: Based in Mölndal, Sweden with some remote work possible
Travel: limited


Apply by October 19, 2025. Interviews will be held continuously. Visa mindre

I Mölndals stad är vi stolta över att ha Sveriges viktigaste jobb där vi tillsammans skapar bästa möjliga vardag för våra medborgare. Med kunskap, mod och kreativitet utvecklar vi våra verksamheter och bidrar till att Mölndal blir en ännu bättre plats att leva och jobba i. Välkommen att göra skillnad i människors vardag varje dag!

Bygg- och miljöförvaltningen arbetar på uppdrag av byggnadsnämnden och miljönämnden. Vår målsättning är att vara den myndighet vi själva vill möta, göra det enkelt att göra rätt och att vi ger bästa möjliga service. På förvaltningen arbetar ungefär 60 personer och arbetet leds av en förvaltningschef och fem enhetschefer. Vi alla arbetar tillsammans för att göra skillnad för invånare och näringsliv i Mölndal. Förvaltningen har lokaler i stadshuset vid Mölndals innerstad.


ARBETSUPPGIFTER
Vi söker nu dig som vill vara en del av vårt team och arbeta som miljöinspektör med fokus på hälsoskydd.

Det är ett variationsrikt arbete och som miljöinspektör hos oss ansvarar du för planering, genomförande och uppföljning av inspektioner, handläggning av ärenden och tillsyn enligt miljöbalken, med särskilt fokus på hälsoskydd. En viktig del av arbetet är att ge råd och information till verksamheter och allmänheten.

Du förväntas också delta i vårt arbete med ständiga förbättringar och verksamhetsutveckling, där vi har ett särskilt fokus på digitalisering och hållbarhet.


KVALIFIKATIONER
Du har en relevant högskole- eller universitetsutbildning inom miljö- och hälsoskyddsområdet. Du har goda kunskaper i miljölagstiftning, förvaltningslagstiftning och tillsyn inom miljöbalksområdet.

Erfarenhet av tillsyn och prövning enligt Miljöbalken eller tidigare arbete som miljöinspektör är ett krav. Det är meriterande om du har jobbat med hälsoskyddsfrågor.

För att lyckas i rollen behöver du vara effektiv och ansvarstagande med en god förmåga att planera och prioritera. Du har en hög social kompetens och ett professionellt bemötande som skapar förtroende och respekt i kontakten med både kollegor och allmänhet.

Du har lätt för att samarbeta och bidrar aktivt till en god arbetsmiljö. Då vi arbetar med myndighetsutövning är det viktigt att du kan uttrycka dig väl i både tal och skrift och att du har förmågan att göra objektiva och sakliga bedömningar, ställa tydliga krav och fatta beslut.

Vi värdesätter en driven och lösningsorienterad person som vill bidra till att utveckla våra tillsyns- och kontrollmetoder.

Stor vikt kommer att läggas vid personlig lämplighet. Då arbetet innebär resor är B-körkort ett krav.

Välkommen med din ansökan!


ÖVRIGT
I den här rekryteringen gör vi löpande urval, vilket innebär att vi kan kalla till intervjuer innan ansökningstiden har gått ut. Visa mindre

Do you have a passion for chemical compliance, sustainability, and making a real impact in the Life Science industry? Are you motivated by turning complex regulations into meaningful solutions? Then this might be the role for you!
As a Chemical Compliance and Sustainability Specialist (kemikalie- och hållbarhetsspecialist), you will be part of our Regulatory Affairs department consisting of two colleagues, responsible for ensuring global compliance with regulations and legislation for IVD products. You will take the lead on chemical and environmental compliance, while also be part of a collaborative team where we share experiences, support one another, and maintain a positive, open atmosphere. This role offers the best of both worlds: the independence to shape your own responsibilities, and the strong backing of dedicated colleagues who value teamwork and knowledge sharing. It is a unique opportunity to make an impact in both compliance and sustainability while developing in a future-focused environment. 
Examples of tasks:
ensure that the company complies with relevant chemical and environmental regulations. 
responsible for conducting chemical risk assessments and classifying solutions in compliance with applicable regulations.
administer and further develop the company’s chemical management system and ensure the accuracy of chemical inventories and classifications. 
provide training and internal guidance on safe chemical handling and risk communication. 
conduct and support environmental reporting, including CSRD/ESRS compliance. 
be responsible for audits and inspections related to environmental and chemical compliance. 
collaborate across departments (e.g., Quality, R&D, Production) to align chemical safety and sustainability practices.

Qualifications
We believe you are a self-driven and collaborative person with a genuine interest in sustainability and safe chemical management. To succeed in the role, you combine initiative and responsibility with openness and teamwork, contributing to a positive atmosphere and meaningful progress in our sustainability efforts.
Requirements:
have a university degree in chemistry, environmental science, biotechnology, or similar. 
practical experience from working in a laboratory. 
strong ability to structure, document, and report technical data. 
excellent skills in Swedish and English, both spoken and written.

Meritorious skills and experience:
knowledge of chemical legislation, e.g. REACH/CLP.
knowledge of national legislation, e.g. the Swedish Environmental code (Miljöbalken), Swedish Work Environment Authority (Arbetsmiljöverkets föreskrifter) and flammable products (Myndigheten för samhällsskydd och beredskaps författningssamlingar).
experience with quality management systems (e.g. ISO 13485).
experience working with chemical safety systems and regulatory tools. 
familiarity with sustainability reporting standards (e.g., CSRD/ESRS). 
experience in internal training, audit preparation, or environmental risk analysis.

Interested? 
This is a full-time, permanent position. Start date by agreement.
If you have any questions regarding the position you are welcome to contact the hiring manager Linnéa, [email protected]
To apply, please register your profile and send in your application as soon as possible but no later than September 15, 2025. Visa mindre

Location: Gothenburg, Sweden?
Pharmaceutical Sciences at AstraZeneca delivers the therapies of the future through scientific leadership in drug delivery, synthetic route design, and the manufacture of Active Pharmaceutical Ingredients (API) across all AstraZeneca therapy areas. Our vision is to be pharmaceutical science leaders—creating innovative, cost-effective solutions and shaping the diverse therapies of tomorrow.
Are you an enthusiastic, innovative, and motivated Formulation Scientist looking for a unique development opportunity? We invite you to join one of our small molecule formulation teams in the vibrant R&D environment at AstraZeneca’s Gothenburg site. This is a temporary 1-year assignment, starting as soon as possible. This assignment offers you the chance to collaborate with passionate colleagues and multi-disciplinary experts—all working together to advance AstraZeneca’s pipeline.


Responsibilities?
This is a laboratory-based role supporting project teams with your scientific and technical expertise in formulation development. You will design and deliver formulation systems for oral, inhaled, and parenteral administration, with a particular emphasis on liquid formulations. Key aspects of this role include hands-on experimental work and essential characterization such as homogeneity, pH, and particle size measurements, supporting projects from early discovery through preclinical development. Close collaboration with a range of internal partners is essential, including working alongside scientists conducting animal studies to ensure strong alignment between formulator and animal safety technician.
You will be expected to conduct experimental work in accordance with project timelines and comply with all relevant Safety, Health & Environment (SHE), quality, and compliance standards. Working in partnership with other formulators, analysts, and skill experts—including specialists in solid-state chemistry and biopharmaceutics—is central to success. Diligent documentation and clear communication of your results to project teams will also be required.?


Essential requirements?
MSc degree in a discipline relevant to formulation science, pharmaceutical technology, or equivalent qualifications
Experience in formulation development, similar product development, or other relevant laboratory skills
Understanding in formulation handling, administration, and setup of animal studies
Genuine interest in experimental laboratory work and practical problem-solving
Delivery-oriented, with the ability to apply scientific and innovative thinking
Strong communication skills in English, both spoken and written.??



Desirable skills/experience?
Technical competence in drug product formulation development for oral and/or parenteral delivery
Familiarity with appropriate quality standards and regulatory frameworks?



If you are passionate about science and want to make a real impact on patients’ lives, there is no better place to be. Join us at AstraZeneca, where we apply science every day to strengthen and expand our pipeline.
Ready to make a difference? Apply today!?Please send in your application before 28th August 2025. Visa mindre

Inventerare invasiva arter till Jakobi Sustainability AB, 2-4 månader
Vi söker dig som brinner för att leta reda på och dokumentera invasiva arter i naturmiljöer med höga naturvärden i Göteborgs stad och har minst två års arbetslivserfarenhet av naturinventering.
Om oss
Vi är ett naturmiljökonsultföretag som är väl etablerat i branschen. Vårt huvudkontor ligger i Göteborg och övriga kontor i Kalmar, Uppsala, Malå och Luleå. I nuläget är vi cirka 16 medarbetare.
Vi är en värdegrundstyrd organisation. Vår vision är hög biologisk mångfald, motståndskraftiga ekosystem och ett fossilfritt samhälle. Vi tror på att hitta sin passion, driva utveckling, dela kunskap, vara lösningsinriktade och att skapa en stark gemenskap. Vi vill arbeta i en miljö där vi stöttar och inspirerar varandra och når målen tillsammans.
Vår verksamhet består i dagsläget av olika typer av naturmiljöutredningar, utredningar inför miljötillstånd (miljösamordning, MKB, 12:6-samråd med mera), samt rennäringsanalyser. Vi verkar bland annat inom energisektorn, infrastruktur, industri och kommunal planering.
Arbetsuppgifter
Du kommer att arbeta med inventering av invasiva arter i Göteborg stad. Tjänsten består till största delen av fältarbete. En liten del förberedande arbete samt efterarbete i form av dokumentation kan förekomma. Du kommer att registrera arterna i Fieldmaps i mobil eller surfplatta. Inventering kommer att ske i alla förekommande väder under perioden. Resor sker inom Göteborgs stad med kollektivtrafik, cykel eller bil.
Om tjänsten
Tjänsten är en säsongsanställning (visstidsanställning) under perioden ca 10 juni till 15 oktober (datum för början och slut kan variera enligt överenskommelse). Det går även att inventera kortare period, till exempel juni till augusti, då kommer vi att anställa flera inventerare.
Om dig
Du behöver ha för området relevant utbildning om minst 1 år, exempelvis högskoleutbildning eller YH-utbildning i naturvårdsbiologi. Det är ett krav att du har minst 2 års relevant erfarenhet. Du har god förmåga att identifiera invasiva arter i fält samt dokumentera dem i Fieldmaps. Du är van att arbeta i fält i alla väder. Som person är du prestigelös, lösningsfokuserad, kommunikativ och brinner för att leverera goda resultat enligt uppsatta mål. Erfarenhet av arbete i ArcGIS Pro eller QGIS är meriterande.
Det här erbjuder Jakobi Sustainability dig
Ett roligt arbete på en trevlig arbetsplats med höga poäng i vår medarbetarundersökning. Vi prioriterar en god arbetsmiljö. Vårt mål är att alla ska känna sig inkluderade och delaktiga. Vi är ett företag med stora ambitioner som vill göra nytta för så väl våra kunder som samhället i stort. Vi har ett tydligt fokus på biologisk mångfald och hållbarhet.
Kontaktperson för detta jobb
Kontaktperson för denna rekrytering är vår affärsområdeschef Marie Jakobi, tel. 070-345 26 09.
Tillträde enligt överenskommelse. Vi jobbar med löpande urval och intervjuer och tjänsten kan därför komma att tillsättas innan ansökningsdatumet löpt ut. Skicka därför din ansökan så snart som möjligt på mejl till [email protected]. Obs! Märk din ansökan med ”Invasiva arter” i ämnesraden.
Välkommen med din ansökan! Visa mindre

Är du intresserad av forskning och utveckling? Vill du utveckla framtidens hållbara kompositprodukter tillsammans med oss, våra partners och kunder? Gillar du dessutom FEM-beräkningar och har erfarenhet av LS-DYNA, HYPER MESH eller ABAQUS så är det här jobbet för dig!
Vi söker vi nu en beräkningsingenjör som vill stärka upp vår kompositverksamhet. Vårt team består av trevliga kollegor som tillsammans besitter kompetens inom bland annat kompositmaterial, produktutveckling, materialmekanik, provning, tillverkningsteknik och återvinning. Det är många spännande saker på gång hos oss, inte minst inom området elektrifiering och hållbara kompositer och vi vill därför stärka upp vårt team genom denna rekrytering.
Om rollen Som del i vårt team får du en unik möjlighet att bidra med din kompetens i olika projekt inom ett flertal spännande branscher, både inom Sverige och utomlands. Vi hjälper bland annat våra kunder med att ta fram nya kompositprodukter, optimera deras processer eller design och mycket, mycket mer.
Viktiga och förekommande arbetsuppgifter i rollen är:
Konstruktion och dimensionering av kompositstruktur mha FEM-beräkningar samt analytiska modeller
Processutveckling och optimering av kompositproduktion mha numeriska metoder
Kontakt med kunder och samarbetspartners
Ledning av delprojekt och initiering av nya projekt och uppdrag
Rapportering av tekniska resultat vid projektmöten eller i rapporter

Tjänsten är en tillsvidareanställning på heltid och placeringsort är Piteå eller Mölndal.
Vem är du? Vi söker nu dig som har en civilingenjörsexamen inom exempelvis Maskin, Teknisk Fysik eller Samhällsbyggnad och/eller erfarenhet inom beräkningsområdet. Vidare har du erfarenhet av att ha arbetat med LS-DYNA, ANSYS, ABAQUS eller motsvarande programvara.
Du skall ha goda kunskaper i svenska och engelska, både i tal och i skrift. Som person är du noggrann, ambitiös och vetgirig. Du har ett sinne för detaljer och har en förmåga att förklara komplexa tekniska termer för personer i din omgivning. Du är initiativrik och självgående, samtidigt som du trivs i ett team. Du håller dig aktivt uppdaterad om forskningsfronten och industrins behov och ser möjligheter att skapa nya samarbeten inom teknik- och materialutvecklingsområdet.
Krav
Masterutbildning inom relevant ämnesområde så som exempelvis maskinteknik eller teknisk fysik alternativt arbetslivserfarenhet inom beräkningsområdet.
Erfarenhet av att ha arbetat med LS-DYNA, ANSYS, ABAQUS eller motsvarande programvara.
Förmåga att uttrycka dig väl i både tal och skrift på svenska och engelska

Meriterande
 Forskarutbildning inom kompositteknologi eller för tjänsten motsvarande relevant ämnesområde
Flerårig erfarenhet av simulering kopplat till materialutveckling, processutveckling eller produktdesign
Erfarenhet av projektledning

Välkommen med din ansökan! Har du frågor om tjänsten är du välkommen att kontakta David Mattsson, enhetschef Kompositteknik Piteå, +46 10-228 49 43. I RISE rekryteringsprocesser efterfrågar vi inte ett personligt brev. I stället ber vi dig besvara ett antal urvalsfrågor som hjälper oss att bättre förstå din kompetens och erfarenhet i relation till den utlysta tjänsten. Sista ansökningsdag är 10 augusti, 2025. Urval kommer starta i samband med sista ansökningsdag. Våra fackliga representanter är Ingemar Petermann, SACO, +46 10 228 41 22 och Linda Ikatti, Unionen, 010-516 51 61.
Samtal från externa rekryteringsföretag och säljare undanbedes vänligen då vi lyder under Lagen om offentlig upphandling. Visa mindre

Are you an experienced drug discovery scientist with expertise in pharmacokinetics, pharmacology and drug metabolism (DMPK)? Would you like to apply your expertise in a global company that follows the science and turn ideas into life changing medicines? Then you could be the new colleague we are looking for!
We are now looking for an experienced and motivated individual to join the team as a DMPK Project Leader. The position is placed at AstraZeneca’s dynamic R&D site in Gothenburg, Sweden. Working at AstraZeneca means being entrepreneurial, following the science, scrutinizing data and details simultaneously with holistic thinking and through teamwork make progress. Your level of professional experience will be relevant for your initial career level (Associate Principal Scientist or Principal Scientist).
Respiratory & Immunology (R&I) is one of the three main therapeutic research areas within AstraZeneca. Early R&I is a global function, with research units in Gaithersburg (US), Cambridge (UK) and Gothenburg (Sweden), and delivers candidate drugs into late-stage clinical development. DMPK interacts with other functions in supporting Early R&I projects all along the value chain, from target selection all the way to market launch and Life cycle management.
What you’ll do:
With a true passion for drug discovery you will support our portfolio within the R&I therapeutic area. In the DMPK project lead role you will work collaboratively with project representatives from other disciplines. These may include biology, antibody Discovery/Protein Engineering, medicinal chemistry, safety, clinical pharmacology, and pharmaceutical sciences, where your task is to influence candidate profiling by providing the necessary DMPK support for clinical investigations.
It is your responsibility to ensure delivery of all DMPK related activities. These include preclinical PK experiments, in vitro ADME and biotransformation to yield pharmacokinetic understanding. Furthermore, assisting design of pharmacodynamic studies that ultimately delivers a pharmacological assessment underpinning human dose prediction.
You will work on projects from candidate selection to Phase 2a. We believe that you have a solid understanding of DMPK, a working knowledge of pharmacology, and that you will be able to provide expert advice and interpretation of complex drug discovery data.
Main Duties and Responsibilities
• Communicate scientific progresses both externally and internally
• Deliver DMPK input and data to projects within agreed timelines and to the right quality
• Apply an understanding of DMPK to support/influence compound profiling, project progression and project strategy
• Define and deliver a translational quantitative PKPD strategy in projects, so that effective conclusions can be made
• Contribute to estimation of safety margins and report results and interpretations to project teams and internal governance bodies
• Responsible for leading, coordinating and engaging with R&I DMPK colleagues in project related activities
• Prepare clear presentations related to the above for internal governance bodies

Essential requirements:
• PhD or equivalent experience in a relevant field
• Expert in DMPK sciences with profound knowledge of drug discovery and development processes
• Broad experience across different modalities (small molecules & biologics) drug development (PK & Bioanalysis)
• Experience with regulatory submissions for biologics and small molecules
• Good knowledge of all DMPK assays including the use of in silico tools for PK prediction
• Experience in project leadership
• Collaborative mindset
• Team player
• Proactive and good communication skills

Why AstraZeneca?
At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.


Work policy:
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Visa mindre

Job description
Research Scientist - NGS based Proteomics
At AstraZeneca, our achievements stem from scientific excellence. Our innovative work thrives on collaboration, ensuring that every member of our team understands how their role contributes to our broader mission of showcasing the power of science.
The NGS/Transcriptomics team is a dynamic group dedicated to advancing “omics” technologies and methodologies. Our goal is to generate insightful data that enhances our understanding of drug pharmacology, target mechanisms, model systems, patients, and diseases, aligning closely with AstraZeneca’s strategy for Growth through Innovation.
We are seeking a Research Scientist with a background in molecular biology laboratory practices. The ideal candidate will possess exceptional teamwork skills and a history of collaborative success to drive scientific excellence and deliver robust results for our research projects.
Are you driven to push the boundaries of science? Do you want to contribute directly to AZ’s innovative growth strategy? If yes, we invite you to join us at our R&D facility in Gothenburg, Sweden!
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.
Deadline 2024-05-02 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Responsibilities
This role is for a lab-based Research Scientist with knowledge and experience in transcriptomics / proteomics. This is a hands-on laboratory-based role with focus on effective delivery to support various clinical and preclinical projects across multiple diseases, species and drug modalities.
In this role you will:
Utilize prior practical laboratory experience in molecular biology.
Contribute to planning and execution of projects involving new omics technologies.
Implement innovative processes developed by the NGS Tx team.
Maintain laboratory processes and equipment rigorously.
Provide experimental support to fellow team members, fostering a collaborative environment.
Ensure compliance with Safety, Health, and Environmental regulations as well as AstraZeneca’s corporate responsibility policies.
Develop a comprehensive understanding of the pharmaceutical industry and identify opportunities for new business initiatives.
Be collaborative with a wide range of scientists of different backgrounds to ensure the highest quality of research.
Implement cutting edge protocols for the simplification and dissection of multiomic environment.

If you are interested, apply now!
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country where the role is advertised.

Qualifications
Essential for the role:
B.Sc. degree or higher in a relevant scientific discipline
Excellent practical and theoretical knowledge and understanding of molecular biology techniques.
Hands-on experience with at least one Next Generation Sequencing / Transcriptomics / Proteomics technology (NGS based proteomics technology, RNA-seq, DNA-Seq, Genotyping methodologies, mass spectrometry).
Familiarity with all aspects of the research process, from hypothesis generation to experimental execution, including sample preparation, data generation, and analysis.
Excellent organizational and communication skills.

Desired qualifications:
Research experience in Pharma/Biotech, medical, or academic environments.
Experience in high-throughput workflows, including the integration of automation in routine laboratory practices.
A record of high-quality peer-reviewed publications or scientific presentations.
Experience in statistics, quantitative data analysis, data mining, and familiarity with LIMS (Laboratory Information Management Systems).


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job Description
Avantor is currently looking for multiple motivated Lab Support Assistants to join the expanding team in Mölndal, Gothenburg! In this diverse role, you will provide operational support to different laboratories on-site by for instance, managing waste, delivering glass was, placing orders and much more. Are you customer minded and highly motivated? On top of this, are you ready for a new professional challenge in an international environment and do you have a general interest in science? Then this might be the opportunity for you! Interested? – Let’s talk!
Maybe you are working in logistics, hospitality or retail but have an interest in science, this could be your opportunity to transition your career into the laboratory world!
This role is a full-time and permanent position based at our customer site, GoCo Health Innovation Centre, in Mölndal. Next to an attractive salary, we offer multiple benefits such as a bonus plan, pension scheme and Health Care allowance. You get to work at a site where multiple smaller scientific and pharma companies are located, enabling you to establish a large network within the industry.
Working hours: Monday to Friday.
The team
The Lab Support Assistant will work in a recently created team of 6 in total, currently already including a Campus Service Lead, Campus Service Assistant and a Campus Service Coordinator. The team belongs to our department Lab & Production Services, supporting leading pharmaceutical companies and laboratories all over the world, in Research and Development within the Life Sciences industry.
What we’re looking for
Education: as a Lab Support Assistant, Lab Technician or similar is a great asset
Experience:
In a hospital or similar environment is preferred
In a lab environment is a plus

Preferred qualifications:
Strong skills in Microsoft Office
Preferably good in both English and Swedish
Service minded, flexible and a good team player
Highly organized, motivated and innovative

How you will thrive and create an impact
Handle goods by shipping and receiving them and by unpacking consumables and chemicals
Refill lab materials, such as glass wash, consumables, lab coats, lab clothes, media, sterile goods etc.
Autoclave lab instruments and clean lab equipment
Manage waste and glass wash
Support in purchasing by placing orders with suppliers and following up on them
Calibrate and review lab equipment such as pipets
Participate in creating work instructions Visa mindre

Job description
Scientist in Advanced Drug Delivery, AstraZeneca Gothenburg
At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.
Pharmaceutical Sciences at AstraZeneca delivers the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) and drug products. Advanced Drug Delivery (ADD) resides within Pharmaceutical Sciences with a mission to provide novel products to AstraZeneca’s clinical pipeline. Our portfolio of projects spans traditional small molecules, peptides, oligonucleotides to RNA based therapeutics across AstraZeneca’s therapy areas.
We are now recruiting a talented and motivated Scientist in the formulation area to join our New Modality Preformulation team within the Advanced Drug Delivery (ADD) function in Gothenburg, Sweden for a parental leave cover .
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.
Deadline 2024-04-18 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Responsibilities
This is an exciting role where you will act as a key member of various project teams and provide your technical and scientific expertise into formulation design of biomacromolecules within the new modality area. As a Scientist you will support drug projects from a formulation perspective in the discovery phase of the drug development process, working from target identification to candidate drug nomination. The role covers development and characterization of formulations of oligonucleotides of high complexity. You will support drug projects within your own function in the preclinical phase and you will serve as a member of the cross-functional drug development project teams, representing your function and scientific area. You will work in close collaboration with formulation scientists, analytical chemists as well as biopharmaceutics experts in Gothenburg, Sweden but also with colleagues in Cambridge, UK and Waltham, US.
If your passion is science & technology and you want to be part of a team that makes a positive impact on patients’ lives, then there’s no better place to be. With us there are many opportunities to develop yourself and your career. From our diverse portfolio and teamwork to our cutting-edge innovations – it’s a place for lifelong learning.

Qualifications
Essential for the roles
Masters or PhD degree in relevant scientific discipline (e.g., Analytical Chemistry, Biochemistry, Biotechnology or Pharmacy)
Previous experience of working with biomacromolecules (e.g. RNA, proteins or peptides) or formulations of small molecules.
Ability to work independently in a laboratory setting.

Desirable:
Industrial experience in a pharmaceutical environment.

Soft skill:
Scientific interest in exploratory formulation/characterization work related to complex molecules, delivery systems and new technologies.
Ability and desire/willingness to effectively communicate, network and build collaborative relationships with partners across disciplines?and cultures, internally and externally and independently lead and influence projects.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

I Mölndals stad är vi stolta över att ha Sveriges viktigaste jobb där vi tillsammans skapar bästa möjliga vardag för våra medborgare. Med kunskap, mod och kreativitet utvecklar vi våra verksamheter och bidrar till att Mölndal blir en ännu bättre plats att leva och jobba i. Välkommen att göra skillnad i människors vardag varje dag!

Bygg- och miljöförvaltningen arbetar på uppdrag av byggnadsnämnden och miljönämnden. Vår målsättning är att vara den myndighet vi själva vill möta, göra det enkelt att göra rätt och att vi ger bästa möjliga service. På förvaltningen arbetar ungefär 60 personer och arbetet leds av en förvaltningschef och fem enhetschefer. Vi alla arbetar tillsammans för att göra skillnad för invånare och näringsliv i Mölndal. Förvaltningen har lokaler i stadshuset vid Mölndals innerstad.

ARBETSUPPGIFTER
Vi söker dig som vill vara en del av vårt team och arbeta som miljöinspektör med fokus på förorenade områden.

Det är ett variationsrikt arbete och som miljöinspektör hos oss ansvarar du för planering, genomförande och uppföljning av inspektioner, handläggning av ärenden och tillsyn enligt miljöbalken, med särskilt fokus förorenade områden. Arbetsuppgifterna kommer främst vara att driva ärenden, göra ansvarsutredningar och riskklassningar samt ansvara för att söka statliga bidrag för undersökningar och åtgärder.

Du förväntas också delta i vårt arbete med ständiga förbättringar och verksamhetsutveckling, där vi har ett särskilt fokus på digitalisering och hållbarhet.


KVALIFIKATIONER
Du har en relevant högskole- eller universitetsutbildning inom miljö- och hälsoskyddsområdet. Du har goda kunskaper i miljölagstiftning, framför allt inom miljöbalkens 10 kap, förvaltningslagstiftning och tillsyn inom miljöbalksområdet. Erfarenhet av tillsyn och prövning enligt Miljöbalkens 10 kapitel är ett krav. Det är meriterande om du har drivit egeninitierad tillsyn och sökt statliga bidrag.

För att lyckas i rollen behöver du vara effektiv och ansvarstagande med en god förmåga att planera och prioritera. Du har en hög social kompetens och ett professionellt bemötande som skapar förtroende och respekt i kontakten med både kollegor och allmänhet.

Du har lätt för att samarbeta och bidrar aktivt till en god arbetsmiljö. Då vi arbetar med myndighetsutövning är det viktigt att du kan uttrycka dig väl i både tal och skrift och att du har förmågan att göra objektiva och sakliga bedömningar, ställa tydliga krav och fatta beslut.

Vi värdesätter en driven och lösningsorienterad person som vill bidra till att utveckla våra tillsyns- och kontrollmetoder

Stor vikt kommer att läggas vid personlig lämplighet. Då arbetet innebär resor är B-körkort ett krav.

Välkommen med din ansökan!


ÖVRIGT
I den här rekryteringen gör vi löpande urval, vilket innebär att vi kan kalla till intervjuer innan ansökningstiden har gått ut. Visa mindre

Job description
Formulation Scientist /Product Developer to AstraZeneca Gothenburg
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
The arena:
We now have the opportunity for one or several consultants to join our team in the role as Formulation Scientist/Product Developer within the department Oral Product Development at AstraZeneca in Gothenburg. The assignment is for the year 2025 on a temporary basis.
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.
Deadline 2024-03-21 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Responsibilities
Tasks and responsibilities/The role:
We are looking for a formulation scientist who can work together with us with generating and evaluating pharmaceutical technologies and formulations. The work includes development, characterization, and documentation, mainly of solid based formulations, in order to develop drug products.
The tasks include planning and implementation of experiments with the aim of generating new formulations and optimizing processes in lab and pilot scale. We are looking for both people with and without previous experience in the area.

Qualifications
Essential for the role:
MSc/BCs in chemistry, pharmacy, chemical engineering, food technology or equivalent.
Good knowledge in written and spoken Swedish and/or English is necessary
laboratory experience including working with computerized systems.
If you have experience from working within the pharmaceutical industry, medical tech, or with manufacturing equipment, this will be an advantage.
Solid materials/formulation experience is highly meriting.

Desirable requirements:
As a person, you should be well organized, analytical, flexible and accurate.
Good team working skills are also important, together with the ability to operate independently.
Good communication skills linked to the ability to work to tight timelines are highly valued.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
We are now recruiting an Assoc. Princ. Scientist Bioscience with knowledge of in vivo experimental biology to join the Bioscience Renal in vivo team within the Early Cardiovascular, Renal and Metabolism (CVRM) therapeutic area. The position is placed at AstraZeneca’s dynamic R&D site in Gothenburg, Sweden.
As Assoc. Princ. Scientist with the Bioscience department at AstraZeneca you will be part of a vibrant team that focus on finding new treatment options to patients with renal disease. In the in vivo team we work with various pre-clinical models and different drug modalities. You will take part in in vivo deliveries to drive the renal pipeline. At AstraZeneca you will work together with experts from different functions and be part of project teams.
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.
Deadline 2024-03-06 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Responsibilities
Independently design, plan and perform high quality in vivo experiments in preclinical models of renal disease
Identify and implement new models/assays relevant for renal disease area
Analyse fluids for biomarker quantification
Perform conceptual interpretation and presentation of generated data
Act as Bioscience representative in assigned projects
Potentially act as new Target Champion, ie proactively identify and develop new target ideas into projects
Deliver data, presentations, reports and regulatory documents
Show scientific leadership in areas associated with the role – renal pathology and pathophysiology – by presenting data internally in key forums
Ensure that own work and work with others is performed according with appropriate safety, health and environment (SHE), qualify and compliance standards, e.g. General Laboratory Standard (GLS)


Qualifications
Essential for the role:
PhD in biology, physiology, pathology or medicine or other relevant areas
Extensive hands-on experience in running in vivo experiments in rodents with experience in renal models
Educated and certified for in vivo experimentation
Proven publication record
Strong oral and written communication skills. English is essential, Swedish is appreciated but is not a requirement

Desirable for the role:
Flexibility & independence
Experience working with preclinical contract research organizations
Expertise in renal physiology and/or pathology
Experience from Pharmaceutical industry


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
Research Scientist Chemistry, Compound Management


Are you a passionate scientist, eager to join a company at the forefront of sample management technologies? Would you like to contribute to the continuous improvement of life-changing projects? Perfect, we have a new challenge for you!
We are looking for a motivated and engaged team member for our Compound Management team at our vibrant R&D site at AstraZeneca in Gothenburg, Sweden.
In this role you will be responsible for the storage and timely supply of compounds to AstraZeneca’s drug discovery projects. Highly automated liquid handling systems will be employed to supply molecules to AstraZeneca scientists and partner organisations. You will be a part of the Discovery Sciences organisation, operating within a first-class scientific environment to support drug discovery across each of AstraZeneca’s Therapeutic Areas.
Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment.
What you will do:
In this position, you will get the opportunity to work in a dynamic and enthusiastic environment, whilst delivering critical support to all phases of drug discovery projects and working with a broad range of chemical modalities. You will be supporting projects by providing compounds in the requested format - assay ready plates, serially diluted mother plates, formulations and solids. Bringing in new capabilities and building new processes are core activities within our group, performed in a cross-functional collaboration setting with the drug discovery projects.
You are expected to act upon day-to-day issues that occur whilst processing samples and run Compound Management development projects to ensure continuous improvement within the local team and the global department.
Why AstraZeneca?
Here we are committed to making a difference. We have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities
Designing, performing and interpreting experiments independently to investigate process improvements and evaluate new technologies.
Working closely with internal project teams to meet drug discovery needs.
Rapidly addressing customer queries with regards to Compound Management orders, software, processes and capabilities.
Achieving personal scientific visibility through project contributions, internal presentations and publications.

We work collaboratively within our Compound Management team to understand the customer needs and how to add value through our experience and capabilities. To maintain this position and provide support within agreed service levels, we actively seek ways to improve our process and exploit new technologies.
Deadline 2024-02-27 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Qualifications
Essential for the role:
Compound Management is a highly collaborative group, working to tight delivery schedules - so the ability to be comfortable working at a fast, goal-oriented pace, with a team-focused attitude, is essential to being successful in the role. Furthermore, you have excellent communication skills with a proactive delivery and customer-focused approach. Explain how
We also believe that you have:
A BSc/MSc in Chemistry/Biotechnology/Chemical engineering
Excellent communication skills and high work ethics.
Excellent problem-solving skills and ability to identify and implement improvement activities.
A track record in the performance of a range of practical skills, including non-routine complex tasks, to a high level.
Passion for science, technology and innovation and understands the drug discovery process

Desirable for the role:
Previous experience of working in a compound management role and operating integrated automation equipment like liquid handlers and scheduling software is a strong merit.
Some experience with IT (/Python/Java coding) is an advantage but not a requirement.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.
With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
Senior Scientist, In Vitro Cardiovascular Biology
Do you have expertise within in vitro cardiovascular biology and enjoy working in the lab? Would you like to apply your expertise in a global company that is accelerating innovative science and turn ideas into life changing medicines? Join us to discover future treatment of Cardiovascular, Renal and Metabolic diseases!
At AstraZeneca, we work at the cutting edge of science to develop the ground-breaking medicines of the future – here we do things that have never been done before. We put patients first and strive to meet their unmet needs worldwide.
CVRM is one of three main therapeutic research areas within AstraZeneca. Early CVRM has a patient-centric approach for discovering novel treatments for patients with cardiovascular-, chronic kidney- and metabolic disease and delivers candidate drugs into late-stage clinical development. In the Bioscience Cardiovascular department, we focus on identifying and validating new drug targets for treatment of patients with cardiovascular disease and heart failure, as well as evaluating pharmacological aspects, e.g. efficacy and mechanism of action, of potential new drug candidates. The in vitro team delivers key data to projects across all phases of the drug discovery and development process, and we work with different modalities such as small molecules, modified mRNA, antibodies, cell therapy, antisense oligonucleotides and peptides.
We are now recruiting a Senior Scientist with expertise in cardiovascular biology to join the Bioscience Cardiovascular in vitro team within the Cardiovascular, Renal and Metabolism (CVRM) therapeutic area at AstraZeneca in Gothenburg, Sweden.
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.
Deadline 2024-02-27 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Responsibilities
As a Senior Scientist you will play a key role in driving science and projects within the cardiovascular area forward. This is a lab-based role where you will explore novel drug targets with key in vitro data. Collaboration is critical for successful delivery of drug projects, and you will work closely with scientists/teams from a wide range of different functions within AstraZeneca as well as with external partners and collaborators. You will work with in vitro biology using cell lines, pluripotent stem cells (PSC) and primary cardiovascular cells along with molecular and functional biology techniques. You will have the opportunity to try novel techniques and ideas required for progressing existing portfolio and novel science. Responsibilities include:
Independently design, develop and run in vitro studies and assays for target identification and validation
Work with molecular biology methods, imaging and assays for functional readouts such as contractility and cardiac metabolism
Contribute to communications of scientific findings through publications in scientific journals and at meetings
Proactively contribute to a vibrant and innovative working environment where improvements and new ideas are adopted and freely shared


Qualifications
Essential for the role:
PhD or master’s degree in biology, pharmacology, cardiovascular disease or similar
Strong experience in cell and molecular biology, biochemistry and relevant in vitro/ex vivo assays within the cardiovascular area
Experience in handling and manipulating relevant PSC cells and primary human and animal cardiac cell types, including cardiomyocytes
Excellent English communication skills, both spoken and in writing

Desirable for the role:
Experience with cardiomyocyte biology and function in healthy and diseased systems
Background in drug discovery and development in the pharmaceutical industry
Background in Vivo and in Vitro


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
Formulation/Analytical Scientist
At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.
Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be “pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future”.
Are you an enthusiastic, innovative, and motivated Formulation/Analytical Scientist seeking a unique opportunity? Join our small molecule formulation team in Advanced Drug Delivery at AstraZeneca’s vibrant R&D site in Gothenburg, Sweden. We offer the experience to collaborate with dedicated team members and to work closely with other skill experts delivering AstraZeneca’s early portfolio.
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities
This is a lab-based role where you will support several drug project teams and provide your technical and scientific expertise into formulation development. You will develop and deliver different formulation systems for oral, inhaled and parenteral use, with a focus on liquid formulations. You will also perform essential characterization work e.g. content, stability, homogeneity, impurity, pH, and particle size measurements, supporting projects in the discovery and preclinical development phase. The role requires a close collaboration with other internal functions to further build our capabilities within advanced drug delivery.
You are expected to perform lab-based experimental work in accordance to project timelines, appropriate Safety, Health & Environment (SHE), quality and compliance standards, and in close collaboration with other formulators and analysts, as well as other skill experts (solid state and biopharmaceutical experts). The work should be documented carefully and to the right quality and standard, and clearly communicated to your project team.
If your passion is science and you want to be part of a team that makes a bigger impact on patients’ lives, then there’s no better place to be. Join us at AstraZeneca, where we truly understand science and apply it every day to strengthen and grow our pipeline.
Ready to make a difference? Apply today!
Deadline 2024-02-14 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Qualifications
Essential requirements:
MSc degree in a scientific discipline relevant to analytical and formulation science (e.g., chemistry, pharmaceutical technology, or equivalent qualifications).
Basic understanding of liquid formulations and basic knowledge of analytical methodologies such as spectrometry and separation science (U/HPLC).
Genuine interest in experimental work and hands-on problem solving.
Delivery focused with the ability to utilize scientific and innovative thinking.
Great communication skills in English, both orally and in writing.

Desirable skills/experience:
Technical competence in the field of drug product formulation development for oral and/or parenteral delivery.
Experience in working with formulation development or similar product development, or other laboratory skills of relevance.
Good understanding of suitable quality standards and regulatory frameworks


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
Scientist in the Microphysiological systems (MPS) Team
Do you have strong experience in cell culture and you would like to apply your expertise in a company that is accelerating innovative science and turn ideas into life changing medicines? Join our Microphysiological systems (MPS) team to discover future preclinical models that can support development of new medications for Cardiovascular, Renal and Metabolic diseases!
At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, and mathematical modelling to help us achieve the next wave of breakthroughs – here we do things that have never been done before. Are you excited to contribute, then you might be the person we are looking for!
This role will be based in the MPS team at the Early Cardiovascular, Renal and Metabolism (CVRM) department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development.
What you’ll do:
You will execute and provide input into the practical delivery of MPS studies and support the development, characterization, and optimization of new models.
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities
Take part in the design, conduct, interpretation and reporting of studies with advanced cell models and MPS.
Carry out various downstream analyses from the cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA’s, qPCR, staining and imaging.
Join further model development activities to support drug projects with MPS data for resolving mechanisms of action, target identification, and candidate drug evaluation.
Effectively communicate and collaborate across the Early CVRM and with the key stakeholders in other functions.

Why AstraZeneca?
At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.
Deadline 2024-02-07 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Qualifications
Essential for the role:


Master’s degree + 2 years of relevant experience.
Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering or similar
Strong hands-on cell culture experience
Experience with primary cells or hPSCs
Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays e.g., ELISAs)
Independent study design, laboratory work, and data analysis
Data visualization and statistical analysis
Excellent interpersonal skills and excellent communication skills in English, both verbal and in writing
Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery

Desired for the role:


Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures
Experience with one or more of cell models for liver, kidney, cardiac, pancreas, or adipose tissue
Experience in culturing immune cells
Handling microfluidic chips
RNA-Seq and proteomics
Workflow automation e.g. robotic liquid handling
Experience from the pharmaceutical industry


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
Flow cytometry Senior Scientist in the Microphysiological Systems (MPS)
Do you have experience in flow cytometry and versatile knowledge in cell culture, and are you eager to apply your expertise in a company that accelerates innovative science to turn ideas into life-changing medicines? Join our Microphysiological Systems (MPS) team and contribute to the discovery of future preclinical models that support the development of new medications for Cardiovascular, Renal, and Metabolic (CVRM) diseases!
At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, flow cytometry, and mathematical modelling to achieve the next wave of breakthroughs – here we do things that have never been done before. Are you excited to contribute? Then you might be the person we are looking for!
This role is based in the MPS team at the Early CVRM department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development.
You will execute and provide input into the practical delivery of MPS studies while also serving as a flow cytometry (FACS) scientist. You will support the development, characterisation, and optimisation of advanced cell models and flow cytometry-based assays. We’ll look to you as an expert in cell and molecular biology techniques, and you will independently carry out various downstream in-vitro analytical methods.
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities


Develop and execute flow cytometry-based assays for cell characterisation and functional analysis including panel design.
Take part in the design, conduct, interpretation, and reporting of studies with advanced cell models and MPS.
Carry out various downstream analyses from cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA, qPCR, staining, and imaging.
Join further model development activities to support drug projects with MPS and flow cytometry data for resolving mechanisms of action, target identification, and candidate drug evaluation.
Effectively communicate and collaborate across the Early CVRM department and with key stakeholders in other functions.
Why AstraZeneca?
At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.

Qualifications
Essential for the role:


Master’s degree + 4 years of relevant experience.
Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering, or similar.
Proficiency in flow cytometry, including assay development, troubleshooting, and data interpretation.
Strong hands-on cell culture experience.
Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays such as ELISAs).
Independent study design, laboratory work, and data analysis.
Data visualization and statistical analysis.
Strong interpersonal and communication skills in English, both verbal and written.
Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery.

Desired for the role:


Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures.
Experience with one or more of the following cell models: liver, kidney, cardiac, pancreas, or adipose tissue.
Experience in culturing immune cells.
Handling microfluidic chips.
Workflow automation, e.g., robotic liquid handling.
Experience from the pharmaceutical industry.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Avantor is currently looking for a motivated Cell Bank Assistant to join the expanding team in Mölndal, Gothenburg. In this position you’ll directly and indirectly support the Cell Bank and take responsibility of managing the storage and supply of cells. Are you a motivated person with high attention to detail and quality? Are you looking for a new professional challenge in an international environment and do you have a general interest in sciences? Then this might be the opportunity for you! Interested? – Let’s talk!
This job doesn't require a scientifc background! Maybe you’re working in logistics, hospitality or retail but have an interest in science, this could be your opportunity to transition your career into the laboratory world!
The role is a full-time, permanent position, based at our customer site, AstraZeneca, in Mölndal. Next to an attractive salary, we offer multiple benefits such as a bonus, pension scheme and Health Care allowance. You get the opportunity to work in an international, innovative environment.
Working hours: Monday - Friday, start time is between 6:00 - 9:00 and finish time 15:00 - 18:00
The team
This is a brand-new position in a newly created team. Together with three colleagues, you are part of the wider Supply Chain team working onsite. Your team belongs to our department Lab & Production Services, which supports leading pharmaceutical companies and laboratories all over the world, in Research and Development within the Life Sciences industry.
What we’re looking for
Experience:
Some knowledge or experience in logistics is desired
Any previous Lab and/or biological background is considered an asset
Biological Sample handing is a plus
Experience in coordinating shipments and/or shipping is an advantage

Preferred qualifications:
Good knowledge of MS Office
Strong communication skills in English; Swedish is a plus
Social, customer centric and service minded
Hands-on, hardworking, and motivated
Attention to detail, organized

How you will thrive and create an impact
Handle frozen cell including, receiving, logging, labeling, storing, tracking, dispatching, returning and/or dipsosing
Register cells and update the database, ensuring the sample tracking system is accurate
Pick and dipstach cells to external sites and for internal collection by scientists
Coordinate shipments and prepare samples for quality control testing
Manage relevant inventory such as Cell boxes, dry ice etc.
Update work instructions when needed and contribute to the design of work routines Visa mindre

Avantor is currently looking for multiple motivated Lab Assistants to join the expanding team in Mölndal, Gothenburg! In this diverse role, you will provide operational support to different laboratories on-site by for instance, managing waste, delivering glass was, placing orders and much more. Are you customer minded and highly motivated? On top of this, are you ready for a new professional challenge in an international environment and do you have a general interest in science? Then this might be the opportunity for you! Interested? – Let’s talk!
Maybe you are working in logistics, hospitality or retail but have an interest in science, this could be your opportunity to transition your career into the laboratory world!
This role is a full-time and permanent position based at our customer site, GoCo Health Innovation Centre, in Mölndal. Next to an attractive salary, we offer multiple benefits such as a bonus plan, pension scheme and Health Care allowance. You get to work at a site where multiple smaller scientific and pharma companies are located, enabling you to establish a large network within the industry.
Working hours: Monday to Friday, with flexibility to start between 6:00 and 09:00 and free to leave between 15:00 and 18:00
The team
The Lab Assistant will work in a recently created team of 6 in total, currently already including a Campus Service Lead, Campus Service Assistant and a Campus Service Coordinator. The team belongs to our department Lab & Production Services, supporting leading pharmaceutical companies and laboratories all over the world, in Research and Development within the Life Sciences industry.
What we’re looking for
Education: as a Lab Assistant, Lab Technician or similar is a great asset
Experience:
In a hospital or similar environment is preferred
In a lab environment is a plus

Preferred qualifications:
Strong skills in Microsoft Office
Preferably good in both English and Swedish
Service minded, flexible and a good team player
Highly organized, motivated and innovative

How you will thrive and create an impact
Handle goods by shipping and receiving them and by unpacking consumables and chemicals
Refill lab materials, such as glass wash, consumables, lab coats, lab clothes, media, sterile goods etc.
Autoclave lab instruments and clean lab equipment
Manage waste and glass wash
Support in purchasing by placing orders with suppliers and following up on them
Calibrate and review lab equipment such as pipets
Participate in creating work instructions Visa mindre

Job description
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives- and are made to feel valued, energized and rewarded for their ideas and creativity. In AstraZeneca we set pride to drive the development in a sustainable way, in all areas of our business from influencing our suppliers through development to commercial products.
We are looking for a scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products, and can work together with us determining the quality attributes during the development of the formulations. The work includes analytical testing , documentation, and attending and presenting in project team meetings. The role is primarily laboratory based.
This is a consultant assignment with a start in January with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities
We are looking for a scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products, and can work together with us determining the quality attributes during the development of the formulations. The work includes analytical testing , documentation, and attending and presenting in project team meetings. The role is primarily laboratory based.
Deadline 2024-11-12 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Qualifications
BSc or MSc typically from pharmaceutics, chemistry, or analytical science, but also other disciplines with relevant skills.
Good knowledge in written and spoken Swedish and/or English is necessary.
Scientific knowledge within analytical science,
Laboratory experience including working with computerized systems and chromatography techniques (e.g. UPLC) for detection of small molecules.



Desirable:
Experience from working within the pharmaceutical industry, this will be an advantage
Well organized, analytical, flexible and accurate.
Good team working skills are also important, together with the ability to operate independently.
Good communication skills linked to the ability to work to tight timelines are highly valued.
If you have experience from working in a GMP environment or worked in AstraZeneca or pharmaceutical industry, this will be an advantage.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.
With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Heres a chance to join our dynamic team at Ribocure Pharmaceuticals AB as an SML, where you will contribute in Ribocures mission to build a world-leading RNA therapeutics R&D company in Sweden and help patients all over the world. We are dedicated to developing innovative treatments that make a difference in patients' lives. At Ribocure, we foster a culture of excellence and are committed to the highest standards of quality in everything we do.
We are now searching fora highly motivated colleague to join our Clinical Sample Management Team.
About the Job
As ourSample Management Lead you will playa coordinating role in a cross-functional setting. The responsibilities cover the entire life cycle of our clinical samples, from protocol development to sample analysis and destruction, including laboratory vendor selection and contracting.
The career level will be adjusted based on the candidate's experience, allowing for flexibility in responsibilities and expectations
Key Responsibilities of the Position1. Laboratory Vendor Selection and Contract Management Lead the identification, selection, and contracting of appropriate laboratories for Pharmacokinetic- (PK), Pharmacodynamic- (PD) and Anti-Drug Antibodies (ADA) analysis.
Collaborate closely with the Clinical Operations Trial Lead and cross-functional experts from various departments like Bioanalysis, Pharmacology, Medical, Translational Science and Clinical Pharmacology to ensure that selected laboratories and assays meet scientific and regulatory requirements.
2. Contribute to Clinical Trial Protocol development and support Regulatory and Ethical Committee submissions Ensure sample collection time points are cost efficient and patient/site centric in regards of blood volumes collected and operational aspects from a site perspective.
Review of trial participant information and the Informed Consent Form.
Responsible for Biobank applications, when applicable.
3. Clinical Sample Management and Lab Kit Supply Coordination Ensure accurate lab kit development and site supply, as well as lab manual development/review.
Training of site staff and CRAs at Site Initiation Visits and continuous support throughout the trial.
Responsible for clinical trial-level sample management, ensuring that samples are delivered from the right patients to the laboratory at the right time.
Ensure Data Transfer Agreements are in place.
4. Data Tracking Oversight and Issue Resolution Coordination Work closely with Clinical Operations, Clinical Pharmacology/Modeling, Medical and selected vendors to ensure critical data is available, analyzed and transferred in a timely manner.
First point of contact and coordinating troubleshooting of PK, ADA and PD sample analysis and assay issues, and proactively anticipating and mitigating potential problems.
5. Communication and Process Improvement Proactively communicate updates and timelines to stakeholders, provide advice and guidance on the sample management process
Collaborate with preferred vendors and quality assurance personnel to develop improvements in the sample management process.
6. Biobank Support the Ribocure Biobank manager in biobank related activities, such as handling of clinical samples, drafting Material Transfer Agreements and assisting in the annual quality control.
Essential Requirements
You must live in the proximity of Gothenburg, Sweden, to be qualified for this position.
University degree, preferably in pharmaceutical sciences, pharmacology, biomedical engineering, biochemistry, biological science, or discipline associated with medicine or clinical research
Minimum of 3 years’ experience in the pharmaceutical or biotech industry
Hands on experience and/or technical knowledge related to different methods and assays used for analyzing PK, ADA, PD and biomarkers (particularly different ELISA techniques, MSD and LC-MS)
Strong competence in English communication, both in writing and speaking
Ability to work independently as well as in a cross-functional setting
Proven ability to coordinate effectively and manage multiple tasks simultaneously in a fast-paced and dynamic work environment
Desirable Requirements Experience of working in a global context where you appreciate and understandcultural differences
Experience in clinical development, working with clinical trials and central lab activities as a sponsor, CRO, or at the site level
Experience of setting up bioanalytical and/or PD assays and related trouble shooting
Experience in biobanking, including handling regulatory requirements, compliance, and operational processes


Our offerWe offer a competitive salary, comprehensive benefits package, and opportunities for growth and advancement. The career level will be adjusted based on the candidate's experience, allowing for flexibility in responsibilities and expectations. We are an equal opportunity employer and welcome applicants from all backgrounds.
We invite you to joinour fast-expanding global organization towards being one of the leading players in oligonucleotide therapeutics.
If you believe this job would be a good match for you, apply as soon as possible but no later than December 15th, 2024.Kindly note that we will assess candidates on a continuous basis.
You apply easily here using the Send Application button where youwill be able to upload CV and cover letter in the system.
Welcome! Visa mindre

Job description
At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.
Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be “pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future”.
We’re looking for talented and motivated solid-state scientists to join our solid state and automation team within Early Product Development and Manufacturing (EPDM) in Gothenburg.
You would join a highly collaborative team and help us deliver the solid-state science to product development within the early portfolio from discovery up into phase II.
To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
The successful applicant will become a core member of the global Solid-state skill area which is responsible for ensuring suitable physical form screening, selection and control within drug substance and product. You will get the opportunity to apply your excellent crystallography and solid-state expertise to the drug projects you are working in, contributing to the progression of these projects and drive the scientific development within the field of solid-state science at AstraZeneca.
This is a consultant assignment with Randstad Life Sciences with a start in January. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities
Deliver solid state characterisation data in our state of the art laboratory using techniques like TGA, DSC, XRPD and DVS.
Responsible for ensuring suitable physical form screening, characterisation, form selection and control within drug substance and product.
Drive solid state skill area in projects and work closely with analytical, formulation, and biopharmaceutics scientists to drive science and innovation.
Plan and conduct lab-based experimental work in accordance with project timelines.
Run and develop solid state workflows on automation equipment such as weighting robots and liquid handling systems

We are working towards treating, preventing, modifying and even curing some of the world’s most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthrough come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.
Does this sound like your next challenge? Apply today! Deadline 2024-11-28 - the selection process and interviews will be ongoing, so please apply as soon as possible!
For more information: Please contact Malin Fridholm, [email protected]. Please note that applications sent through email will not be processed and deleted due to GDPR.

Qualifications
Essential for the role:
Master/Bachelor graduate with relevant experience in solid-state chemistry, physical chemistry, or related disciplines.
Experience in screening and characterization of solids, analytical methodology, and laboratory-based work.
Experience from conducting solid-state characterization using techniques like TGA, DSC, XRPD, or DVS.

Desirable for the role:
Interest in lab automation, simulation, or prediction is advantageous.
Understanding of how physicochemical and solid-state properties affect drug product development.

Soft skills:
Creativity, innovation, and problem-solving skills.
Ability to assess, review, and report data, and present findings in multi-disciplinary teams.
Flexibility, adaptability, and strong communication, teamwork, and leadership skills.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, manufacturing of Active Pharmaceutical Ingredients (API) and Investigational Medicinal Product (IMP) across all the AstraZeneca therapy areas. Our vision is to be “pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future”.
We’re looking for a talented and motivated Analytical Chemist (Scientist/Senior Scientist) to join our analytical characterization team within Early Product Development and Manufacturing (EPDM) in Gothenburg, Sweden
This role is located in Gothenburg, Sweden.
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.
Deadline 2024-11-29 - the selection process and interviews will be ongoing, so please apply as soon as possible!
For more information: Please contact Malin Fridholm, [email protected]. Please note that applications sent through email will not be processed and deleted due to GDPR.



Responsibilities
In the role as Scientist/Senior Scientist, you would join a highly collaborative team and together we will deliver the analytical science to drug product development within the early portfolio up to phase II. To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus. This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully and to the right quality, as well as contributing to regulatory clinical trial applications (CTA). You will get the opportunity to apply your excellent analytical expertise in the drug product projects you will be working in. You will contribute to the progress of the drug product development, getting new medicines to patients and driving the scientific development within the field of analytical science at AstraZeneca.

Qualifications
Essential requirements:
University degree (MSc, PhD) in relevant discipline, preferable with industry experience
Scientific knowledge within analytical science and technically skilled to use chromatography with relevant detection techniques for small molecules
Broad industry experience of pharmaceutical development including oral solid dosage form development
Experience of CMC regulatory submissions and work according to GMP
In-depth skills in specific analytical techniques for small molecules, e.g. mass spectrometry, NMR, dissolution etc.
Excellent written and oral communication skills in English is a must
Experience, knowledge and keen interest in the field of automation, AI and digitalization would be advantageous
Proven track record in publications related to analytical science or characterisation of pharmaceuticals is desirable

Soft skills:
You are a driven experimentalist, with a passion to deliver highly relevant and reliable data and with the ability to be influential in discussions in a wide set of communities and multi-disciplinary project teams in accordance with project timelines
You keep abreast with the scientific discipline and ability to drive and lead science and innovation personally, within the department and manage external collaborations to meet future needs
You have excellent communication, collaboration, networking and leadership skills & ability to lead and inspire colleagues
At AstraZeneca, we are committed to making a difference. We have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. Here, we think holistically about patients and are always learning from those living with diseases. We harness digital, data science & AI to fast-forward our research, ensuring that work born in a lab can make a real difference. Every day, we impact patients' lives across the world.

About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.
With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

About AstraZeneca
At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.
Chemistry, Manufacturing, and Controls Regulatory Affairs (CMC RA)
Our Chemistry, Manufacturing, and Control (CMC) Regulatory Affairs function spans across the product lifecycle and is responsible for the regulatory strategy relating to the development, manufacture and testing of all of our medicines.
With our expertise we interpret, anticipate and craft global Health Authority expectations to build insightful CMC and Device Regulatory Strategies.
We are the bridge between our R&D functions, Operations sites, Quality and Global Supply Teams in helping safe, effective medicines reach the right patient at the right times. We manage the timely preparation and delivery of CMC contributions to the regulatory submissions linked to medicinal products throughout the product lifecycle; including Clinical Trial Applications (CTAs), Marketing Authorisation Applications (MAAs) and all post approval activities improving the reliability and value of business critical Supply Chain changes to the AZ organization by supplying the regulatory context, intelligence and mentorship for robust approval and change management.
What you’ll do
We are looking for a Chemistry, Manufacturing and Controls Regulatory Affairs (CMC RA) Manager preferably with a Development or New Product Introduction (NPI) focus to join us in Gärtuna (Sweden), with the flexibility to work remotely for up to 2 days a week.
Being a CMC RA Manager for projects in the Development & NPI lifecycle states means that you will effectively manage the production of CMC documentation for designated product ranges to deliver against the needs of both the AZ business and the patients for internally and externally manufactured products. You will project manage global CMC regulatory submissions ensuring that project activities and documentation are delivered to the required standards.
As a CMC RA Manager you will also contribute to and own the regulatory CMC components of business-related projects, applying effective levels of interactive communication with collaborators and project team members to ensure that relevant timelines and regulatory commitments are appropriately communicated. The accountabilities also include responsibility for change management as assigned and to ensure the takeaways from own projects are shared with other co-workers/within the function.
Responsibilities:
Manage/Lead assigned projects; define and agree regulatory submission strategy, coordinate cross-functional preparation of submission content and complete data assessments to ensure the authored regulatory CMC contributions are in line with AstraZeneca and Health Authority requirements throughout the development & NPI product lifecycle stages
Leverage regulatory intelligence to optimise submission content, employing quality risk management as appropriate
Maintain regulatory databases related to submissions
Capture and communicate Health Authority approval status
Continually evolve and develop the organisation’s regulatory expertise; through proactive recording and communication of regulatory insights gained via Health Authority interactions
Build and maintain good relationships with internal and external partners to facilitate regulatory execution and delivery
Contribute to business process optimization activities, removing waste and improving efficiency
Apply GxP principles according to the stage of product lifecycle



Education, Qualifications, Skills and Experience
Crucial for the role:
Bachelor’s degree or equivalent experience in a scientific subject area
Experience in a biopharmaceutical (or related) manufacturing, technical or regulatory environment
Awareness of CMC considerations and how they apply in a regulatory environment
Project management expertise with the ability to plan, coordinate sophisticated programs of work and adapt to changing situations to ensure on time delivery
Effective communication (written and oral) and partner leadership skills
IT Skills



Desirable for the role:
Detailed understanding of current regulatory CMC requirements and the CMC contributions to clinical and/or commercial regulatory dossiers
Knowledge of the drug development and marketing application processes for pharmaceutical products
Direct/indirect Regulatory Affairs CMC experience with clinical (IND & IMPD) or marketing application (NDA or BLA) submissions for synthetics and/or biologic and biotechnology derived products
Understanding of regulations and guidance governing the manufacture of pharmaceutical products
Demonstrated research skills in understanding, interpreting and applying regulations or guidance from external sources; including industry bodies and national competent authorities
Lean capabilities
Understanding and application of appropriate risk management
Proactive in identifying and acting on opportunities to drive operational improvements



Why AstraZeneca?
At AstraZeneca, we 're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. Visa mindre

Scantox Sweden är ett kontraktslabb inom läkemedelsutveckling, på labbet i Mölndal är vi specialister på organisk analytisk kemi. Vår verksamhet baseras på kvalitetskontroller av läkemedelsprodukter för frisläppning till marknaden utefter enskilda kunders specifika behov. Hos oss får du en varierad arbetsdag med påverkansmöjlighet och beslutsansvar för ditt arbete. Kunderna är primärt producenter och importörer av läkemedel & medicintekniska produkter, men även helt andra fält som livsmedel och miljöprover behandlas. Detta i kombination med vår breda instrumentpark med tonvikt på kromatografi ger möjlighet att lära sig nya tekniker och utvecklas inom fältet organisk analytisk kemi.
Du bör ha åtminstone ett par års arbetslivserfarenhet från arbete i den privata sektorn/industrin med analyser under GMP eller ackreditering (ex.vis. ISO17025), endast akademisk erfarenhet är av mindre intresse. Om du är Analytisk kemist, Laborant, Laboratorietekniker, Biomedicinsk analytiker (BMA) eller liknande är du välkommen att söka. Men, det är viktigt att du beskriver dina erfarenheter av GMP-analyser i din ansökan.
Flera kritiska instruktioner är på svenska så du bör behärska språket och din ansökan skall skrivas på svenska.
I rollen som analytisk kemist utför du kvalitetskontroll av läkemedelsprodukter. Du arbetar laborativt enligt upprättade rutiner och ansvarar för att utvärdera och rapportera resultat i LIMS-system. Du måste ha erfarenhet av att självständigt analysera prover med ex.vis. UPLC/HPLC och bedöma resultaten. Har du också erfarenhet av Dissolution-analyser är detta mycket meriterande.
Vi söker dig som är ansvarstagande och har ett noggrant och strukturerat arbetssätt. Arbetet är varierat då vi har många olika produkter för frisläppningsanalys och möjlighet att utvecklas inom många olika analystekniker finns.
Arbetet är heltidsanställning med fast lön. Tjänsten är placerad i Mölndal. Vi har ingen möjlighet att hjälpa till med boende så sökanden med boende inom pendlingsavstånd är meriterande.
Ansökan sker senast 31 okt 2024 genom att skicka CV och personligt brev till [email protected]. Inga ansökningar som skickas via LinkedIn eller andra tjänster kommer att behandlas. Urval och intervjuer kommer att ske löpande så vänta inte till sista ansökningsdag. Kandidater som skickar in underlag godkänner att dessa behandlas under processen. Uppgifterna kommer att raderas senast 6 månader efter att rekryteringen avslutats.
Frågor kan ställas till Rickard Wahlström (Site manager), på [email protected] eller 031-24 22 00. Visa mindre

Job description
Senior Scientist, SPR & Biophysics - Protein Science, Structural Biology and Biophysics
Are you a scientist with expertise and enthusiasm for applying Surface Plasmon Resonance (SPR) and other biophysical tools to uncover molecular interactions and advance drug discovery? Do you want to leverage your skills to broaden the application of SPR and related techniques in impactful drug discovery projects, while growing your career within a company that values science and transforms ideas into life-changing treatments? AstraZeneca has an exciting opportunity for you!
AstraZeneca is committed to the development of next generation innovative medicines. To help us with this we are looking for a scientist with passion, expertise and experience to join our Protein Science, Structural Biology and Biophysics department as a lab-based Senior Scientist on a one-year contract basis within the Biophysics team. The team is based in our vibrant R&D site in Gothenburg, Sweden and applies biophysical technologies across a range of different modalities to support drug discovery from target validation to drug candidate. You will be part of a team of enthusiastic scientists that deliver deep technical and scientific expertise by applying molecular biophysical methods, including SPR, NMR, ITC, DSF, HDX-MS and single molecule approaches. This is a unique opportunity to contribute to the development and execution of research strategies for the discovery of new medicines – and be focused on the field of Biophysics.
Why AZ?
When we see an opportunity for change, we seize it and make it happen, because any opportunity can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey in finding new ways to work, pioneering cutting edge methods and bringing unexpected teams together!
Does this sound like your next challenge and place to work? We look forward to your application.

Responsibilities
The role of Senior Scientist is a laboratory-based position supporting the characterization of molecular interactions in drug discovery, with a focus on Surface Plasmon Resonance (SPR) and other biophysical techniques. We are seeking a highly skilled and motivated biophysicist with deep expertise in SPR assay development, method optimization, and screening to join our team on a one-year contract basis. The ideal candidate will have a strong theoretical and practical background in biophysical techniques, particularly SPR, along with experience in protein-ligand interactions. This role is crucial in advancing our research and development projects across various therapeutic areas.
You will have significant control and influence over project direction, allowing you to shape experimental strategies and outcomes. Additionally, you will have opportunities to learn new techniques and develop your leadership skills. Working in a collaborative and innovative environment, you will engage with scientists from diverse disciplines. This position offers a unique chance for professional development in an industrial setting, helping you gain valuable experience and build a strong foundation for future career growth.
You will be responsible for designing and implementing advanced SPR assays, tailored to specific research needs, as well as larger screening activities. You will conduct intricate experiments aimed at understanding binding kinetics, affinity, and thermodynamics, ensuring accurate and precise data collection and reporting. Your expertise will be crucial in analyzing SPR data, interpreting results, and integrating findings with other research data to provide comprehensive insights into drug mechanisms of action. You will collaborate closely with multidisciplinary teams, contributing to the integration of SPR and biophysical findings into broader research objectives. Additionally, you will keep abreast of the latest advancements in SPR and biophysics, continuously applying this knowledge to enhance our research capabilities.
You will document and present your results in both internal and external meetings, playing a vital role in driving our scientific endeavours forward. Finally, to be successful in this role we see that you have good social and communication skills, are collaborative and a strong team player. You should also be able to work independently and have a positive, goal oriented and problem-solving attitude.
Deadline 2024-10-31 - selection and interviews will be ongoing, please apply as soon as possible!

Qualifications
Ph.D. or equivalent in Chemistry, Biochemistry, or a related field with a focus on biophysical techniques to characterize molecular interactions, preferably SPR (or something similar system)
Proficiency with surface-based biosensor platforms (e.g., Biacore, Nicoya, Octet, WAVEsystem) including assay development and optimization.
Expertise in developing, troubleshooting, and optimizing biosensor assays for high-throughput screening and kinetic data analysis, with proficiency in data analysis software (e.g., Biacore Insight, WAVEcontrol) and protein sample preparation to ensure high-quality samples for biophysical studies.
Familiarity with complementary biophysical methods such as ITC, MST or DSF as well as protein expression, purification, and characterization techniques to ensure optimal sample quality for biophysical assays.
Proven reputation gained through an excellent track record of publications and/or conference presentations.

Desirable for the role:
Worked in drug discovery environment.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Avantor söker för närvarande tre motiverade laboratorieassistenter till det expanderande teamet i Mölndal, Göteborg! I denna mångsidiga roll kommer du att ge operativt stöd till olika laboratorier på plats genom att till exempel hantera avfall, leverera glas, göra beställningar och mycket mer. Är du kundorienterad och mycket motiverad? Är du dessutom redo för en ny yrkesmässig utmaning i en internationell miljö och har du ett allmänt intresse för vetenskap? Då kan det här vara rätt tillfälle för dig! Är du intresserad? - Låt oss prata!
Du kanske arbetar inom logistik, hotell och restaurang eller detaljhandel men har ett intresse för vetenskap, då kan det här vara din möjlighet att byta karriär till laboratorievärlden!
Denna roll är en tillsvidareanställning på heltid med placering hos vår kund, GoCo Health Innovation Centre, i Mölndal. Förutom en attraktiv lön erbjuder vi flera förmåner såsom bonusplan, pensionssystem och friskvårdsbidrag. Du kommer att arbeta på en plats där flera mindre vetenskapliga och läkemedelsföretag är belägna, vilket gör att du kan etablera ett stort nätverk inom branschen.

Arbetstider: Måndag till fredag, med möjlighet att börja mellan 6:00 och 09:00 och sluta mellan 15:00 och 18:00

Teamet
Lab Assistant kommer att arbeta i ett nyligen skapat team på totalt 6 personer, som för närvarande redan inkluderar en Campus Service Lead, en Campus Service Assistant och en Campus Service Coordinator. Teamet tillhör vår avdelning Lab & Production Services, som stöder ledande läkemedelsföretag och laboratorier över hela världen inom forskning och utveckling inom Life Sciences-industrin.

Erfarenhet som krävs
Utbildung: som laboratorieassistent, laboratorietekniker eller liknande är en stor tillgång
Erfarenhet :
· Sjukhus eller liknande miljö är att föredra
· I en laboratoriemiljö är ett plus
Erforderliga färdigheter :
· Goda kunskaper i Microsoft Office
· Gärna goda kunskaper i både engelska och svenska
· Serviceminded, flexibel och en god lagspelare
· Mycket välorganiserad, motiverad och innovativ

Huvudsakliga uppgifter och ansvarsområden
· Hantera varor genom att skicka och ta emot dem och genom att packa upp förbrukningsartiklar och kemikalier
· Fylla på labbmaterial, t.ex. glasrengöring, förbrukningsmaterial, labbrockar, labbkläder, media, sterila varor etc.
· Autoklavera labbinstrument, rengöra labbutrustning
· Hantera avfall och glastvätt
· Stöd vid inköp genom att lägga beställningar hos leverantörer och följa upp dessa beställningar
· Kalibrera och granska labbutrustning såsom pipetter
· Delta i arbetet med att skapa arbetsinstruktioner Visa mindre

I Mölndals stad är vi stolta över att ha Sveriges viktigaste jobb där vi tillsammans skapar bästa möjliga vardag för våra medborgare. Med kunskap, mod och kreativitet utvecklar vi våra verksamheter och bidrar till att Mölndal blir en ännu bättre plats att leva och jobba i. Välkommen att göra skillnad i människors vardag varje dag!

Bygg- och miljöförvaltningen arbetar på uppdrag av byggnadsnämnden och miljönämnden. Vår målsättning är att vara den myndighet vi själva vill möta, göra det enkelt att göra rätt och att vi ger bästa möjliga service. På förvaltningen arbetar ungefär 60 personer och arbetet leds av en förvaltningschef och fem enhetschefer. Vi alla arbetar tillsammans för att göra skillnad för invånare och näringsliv i Mölndal. Förvaltningen har lokaler i stadshuset vid Mölndals innerstad.

ARBETSUPPGIFTER
Bygg- och miljöförvaltningen söker dig som har erfarenhet och är intresserad av att arbeta med tillsyn och prövning inom enskilda avlopp. Det är ett variationsrikt arbete, vilket innebär ansvar för planering, genomförande och uppföljning av inspektioner samt besvara frågor från fastighetsägare och allmänheten. Vi vill att alla på förvaltningen bidrar till ständiga förbättringar och verksamhetsutveckling.

KVALIFIKATIONER
Vi söker dig som har lämplig högskole- eller universitetsutbildning inom miljö- och hälsoskyddsområdet. Du ska ha goda kunskaper i miljölagstiftning, förvaltningslagstiftning och tillsyn inom miljöbalksområdet. Erfarenhet av prövning och tillsyn enligt miljöbalken eller tidigare arbete som miljöinspektör är ett krav. Det är meriterande om du har jobbat med enskilda avlopp.

Som person är du effektiv och ansvarstagande. Du har en god social kompetens som bidrar till att skapa ömsesidigt förtroende och respekt i mötet med de vi möter. I en rådgivande roll kan du på ett professionellt sätt förmedla information. I myndighetsrollen krävs att du har förmågan att göra objektiva och sakliga bedömningar, ställa tydliga krav och ta beslut. Du har en god planerings- och prioriteringsförmåga samt tar ansvar för och slutför dina uppgifter.

Då vi arbetar med myndighetsutövning är det viktigt att du kan uttrycka dig väl i tal och skrift.
Som medarbetare har du en mycket god kommunikations- och samarbetsförmåga och deltar aktivt i samarbetet med dina kollegor på bygg- och miljöförvaltningen och övriga i Mölndals stad. Vi önskar att du vill vara med och utveckla våra tillsyns- och kontrollmetoder med digitalisering i fokus. Stor vikt kommer att läggas vid personlig lämplighet. B-körkort är ett krav.

I mötet med kollegor och de vi möter i vårt uppdrag (verksamhetsutövare, företagare, kommuninvånare) vill vi att du har ett bra bemötande, är driven, mål- och resultatorienterad, samarbetsinriktad och serviceinriktad.

ÖVRIGT
I den här rekryteringen gör vi löpande urval. Välkommen med din ansökan redan i dag! Visa mindre

Job description
Research Scientist Biosamples, Biobank Scientist
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. However, as a company we are more than one of the world's leading pharmaceutical companies, we are proud to have a unique workplace culture that inspires innovation and collaboration. AstraZeneca employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
The arena:
Biobank scientists are responsible for the storage and timely supply of human biological samples (HBS) to AZ research projects. HBS are received from e.g. clinical studies or academic collaborations, stored in local biobanks and distributed to projects. The group primarily supports the Sweden Region but partners with other Biobank groups within AZ globally to provide efficient support across AZ and our partner organisations.
The Biobank group works collaboratively to provide support within agreed service levels with a strong focus on our customers. We strive hard to understand what fits their needs best and to add value through our services. With an increased focus on the value and use of biobank samples we actively seek ways to improve our process or exploit new technology to build a cutting-edge facility.
AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.
This is a consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.
Deadline 2024-09-05 - the selection process and interviews will be ongoing. For more information: Please contact Malin Fridholm, [email protected]
Please note that applications sent through email will not be processed and deleted due to GDPR.

Responsibilities
Tasks and responsibilities/The role:
We are currently recruiting for a Biobank Scientist in the AZ Gothenburg Biobank group within the global Precision Medicine and Biosamples organization. This position will provide the opportunity to work in a dynamic and enthusiastic environment whilst supplying a critical service to drug discovery projects. The work is highly collaborative with the team having a collective responsibility for the overall delivery.
The role is focused on supporting drug discovery projects within R&D Gothenburg by maintaining high quality handling and storage of HBS and support projects with requested samples in a timely manner.
As a Biobank Research Scientist you will be expected to:
Work as part of the team rotating between the following typical tasks
Receive and register incoming HBS
Process requests for HBS to customers, including using automated liquid handler
Manage customer orders using specialized informatics systems as well as databases
Respond to customer queries via mail or telephone
Partner with Biobank groups globally as well as internal and external customers

?The group has a strong emphasis on continuous improvement which takes the form of individual and group projects within the team, the department and across Biobank groups within AZ.
The biobank team is a highly collaborative group working to tight delivery schedules so the ability to be comfortable working at a fast pace with a goal orientated and team focussed attitude is essential. Excellent communication skills with a proactive and service minded approach is key.
Work closely with other groups in the organization
Act upon day-to-day issues that occur whilst processing HBS samples to ensure continuous improvement
Identify initiatives to improve efficiency or quality.


Qualifications
Essential for the role:
University degree in a Bioscience discipline and previous experience of laboratory work handling biological samples.
Previous knowledge and experience (1 year) of biobanking is highly desirable.
Experience of working with various IT solutions, including extensive knowledge of Excel, LIMS systems and database usage, is also a clear advantage.
Experience of automated liquid handling is advantageous.
Good analytical and problem-solving skills involving large and complex datasets is desirable.
Excellent English, both spoken and written



Soft skills:
Ability to plan, perform and evaluate experiments to investigate improvement possibilities in a process.
Knowledge of the regulatory framework of biological samples.
Interest in logistics and developing processes through customer interactions and technology awareness.
Drive and enthusiasm to solve the root cause of problems and not only overcome the presenting problem.
Thrive on working in a committed team and gain satisfaction from the overall performance of the group


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.
With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Fujirebio Diagnostics AB i Mölndal söker en Manufacturing Technician (produktionstekniker) till vårt team. Det är en bred lab support-roll där du kommer stödja labben inom både produktutveckling och produktion. Huvudsakliga arbetsuppgifter är tillverkning av lösningar, filtrering och koncentrering av skördmedium, städning av rum med högre renhetskrav. Även viss disk och autoklavering ingår i tjänsten. Som produktionstekniker arbetar du utifrån våra skriftliga instruktioner och där all tillverkning dokumenteras i batchprotokoll. För mer information samt ansökan: https://www.fujirebio.com/en/careers Visa mindre

Are you an experienced scientist with expertise in pharmacokinetics, pharmacology and drug metabolism (DMPK)? Would you like to apply your expertise in a global company that follows the science and turn ideas into life changing medicines? Then you could be the new colleague we are looking for!
Our team is growing, and we are now looking for two motivated individuals with experience in Biologics and/or small molecule drug development and PKPD, to join us as a DMPK Project Leader, from candidate selection to registration and beyond. These positions are placed at AstraZeneca’s dynamic R&D site in Gothenburg, Sweden. Working at AstraZeneca means being entrepreneurial, following the science, scrutinizing data and details simultaneously with holistic thinking and through teamwork make progress.
Respiratory & Immunology (R&I) is one of the three main therapeutic research areas within AstraZeneca. Early R&I is a global function, with research units in Gaithersburg (US), Cambridge (UK) and Gothenburg (Sweden), and delivers candidate drugs into clinical development. DMPK interacts with other functions in supporting Early R&I projects all along the value chain, from target selection all the way to market launch and Life cycle management.
What you’ll do?
With a true passion for drug discovery you will support our portfolio within the R&I therapeutic area as a subject matter expert. In the DMPK project lead role you will work collaboratively with project representatives from other disciplines. These may include biology, safety , clinical pharmacology, pharmaceutical sciences, antibody Discovery/Protein Engineering and medicinal chemistry, where your task is to influence candidate profiling by providing the necessary DMPK support for clinical investigations.
It is your responsibility to ensure delivery of all DMPK related activities throughout the value chain in accordance with regulatory requirements. These include preclinical PK experiments, in vitro ADME and biotransformation to yield pharmacokinetic understanding. Furthermore, assisting design of pharmacodynamic studies that ultimately delivers a pharmacological assessment underpinning human dose prediction and emerging clinical experience.
You will work as the development DMPK representative on project teams from candidate selection to registration and beyond. We believe that you have a solid understanding of DMPK, a working knowledge of pharmacology, and that you will be able to provide expert advice and interpretation of complex nonclinical and clinical data.
Main duties and responsibilities;
Communicate scientific progresses both externally and internally
Deliver DMPK input and data to projects within agreed timelines and to the right quality
Responsible for delivering and produce the nonclinical pharmacokinetic documentation to support clinical progression
Apply an understanding of DMPK to support/influence compound profiling, project progression and project strategy
Define and deliver a translational quantitative PKPD strategy in projects, so that effective conclusions can be made
Contribute to estimation of safety margins and report results and interpretations to project teams and internal governance bodies
Responsible for leading, coordinating and engaging with R&I DMPK colleagues in project related activities
Prepare clear presentations related to the above for internal governance bodies

Your level of professional experience will be relevant for your initial career level (Associate Principal Scientist or Principal Scientist).
?Essential for the role
PhD or equivalent experience in a relevant field
Expert in DMPK sciences with profound knowledge of drug discovery and development processes
Broad experience in biologics drug development (PK & Bioanalysis)
Have PK modelling skills, experience of human PK and dose prediction, as well as an understanding of disease biology and PKPD
Experience with regulatory submissions for biologics and/or small molecules
Knowledge of all DMPK assays including the use of in silico tools for PK prediction
Experience in project leadership
Collaborative mindset
Team player
Proactive in providing expert support to project team and excellent communication skills

Why AstraZeneca?
At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development. Visa mindre

Are you a passionate and experienced scientist with expertise in molecular biology and recombinant protein expression? Fuelled by our commitment to help more patients, strengthen our pipeline and grow our area. This might be your next challenge!
We are now looking for a Molecular Biologist to join us as a Research Scientist at AstraZeneca in our Protein Sciences department in Discovery Sciences. This department is based in our vibrant R&D site in Gothenburg, Sweden, and is responsible for the delivery of protein reagents to discovery projects. You will be part of a team of enthusiastic scientists to deliver deep technical and scientific expertise in Molecular Biology. This role is an opportunity to contribute to the development and execution of research strategies for the discovery of new medicines.
What you will do
In this role, you will provide key molecular biology expertise for the design and generation of DNA constructs for downstream drug discovery applications such as recombinant expression of protein reagents, reporter gene assays, cell lines, DNA libraries, and recombinant production of proteins for structure and biophysics. We are seeking a highly skilled and motivated Research Scientist to join our dynamic team. The successful candidate will deliver from the lab with construct design and high throughput construct generation.
Essential for the role
MSc in relevant scientific discipline (e.g. Molecular Biology, Genetics, or Bioinformatics), or a related discipline, with relevant experience, preferably in the pharmaceutical or biotechnology industry.
Extensive experience in high throughput cloning techniques such as Golden Gate and Gibson assembly with strong problem-solving skills.
Demonstrated proficiency with automation equipment and programming (e.g. Python) of liquid handlers (BiomekI7 or equivalent).
Demonstrated expertise in Next Generation Sequencing technology including Illumina and Nanopore sequencing with hands on experience and the ability to configure Bioinformatics pipelines.
Strong communication skills, team working and capable of bridging gaps across disciplines.

Desirable for the role
Experience working in LIMS environment and request management systems, e.g., Benchling, Geneious, demonstrated data management experience and excellent level of compliance.
Proven ability to support IT technology development projects.

Why AstraZeneca?
Always advancing our scientific knowledge and helping to shape the future of healthcare for the greatest and swiftest impact on disease. Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment. We truly believe that everyone contributes with a unique set of competence. Your curiosity and passion for personal development combined with support from colleagues, mentors and leaders, will ensure you maximise your skills, abilities and contribution. Visa mindre

Job description
Research Scientist position – in vitro compound profiling
We are looking for a Research Scientist to join our Mechanistic Biology & Profiling function within the Discovery Sciences organization in Gothenburg, Sweden. You will apply proven biochemistry and cell biology expertise to perform in vitro assays, including independent planning, analysis and reporting. Routine profiling will be combined with tailored mechanism of action studies in support of chemistry optimisation across different drug discovery projects.
As an individual you are passionate about laboratory work and want to apply this in a setting where team work and flexibility is critical. You will join a team whose remit is to support our drug discovery projects globally with early DMPK assessment, SAR profiling and detailed mechanism of action data. We offer a highly rewarding scientific environment with ample learning opportunities.
You will be strongly encouraged and supported to think creatively in our dynamic environment. Here, we are free from fear of failure, free to ask the right questions and make bold decisions.
Why AstraZeneca in Gothenburg?
You can ask anybody who has ever set foot here – our Gothenburg site has a vibrant culture that pulls you in! It is a mix of both local and international talent. We welcome the contribution of people from all backgrounds, beliefs and walks of life.
So, what’s next? If this sounds like your next challenge - please apply today!


Deadline 11th of July - the selection process and interviews will be ongoing. The starting date will be in August.
For more information: Please contact Katan Ali, [email protected].
Please note that applications sent through email will not be processed and deleted due to GDPR.
This is an consultant assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.





Responsibilities
This is a lab-based role focused on generating routine screening data and bespoke in vitro pharmacology studies in support of drug discovery projects. The work includes independent troubleshooting and timely reporting of data according to agreed timelines. All work is conducted in close dialog with project teams, specifically in support of the Cardiovascular, Renal and Metabolism as well as Respiratory & Immunology disease area organisations locally in Gothenburg.

Qualifications
Essential for the role:
A strong passion for laboratory work.
MSc or PhD within a relevant scientific discipline or demonstrated relevant experience in the Life Science industry.
Proven track record of in vitro pharmacology studies.
Excellent communication skills and an ability to operate effectively in a multi-disciplinary research environment.
Independent analysis and evaluation of complex data and delivery of data to agreed timelines.
First-rate decision-making skills, coupled with tenacity to see decisions through, even in situations of ambiguity.



Desirable in the role:
Compound profiling in a screening environment using microtiter plates and automation.
Experience with either enzymology studies or mechnistic cell-based studies.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Avantor letar för närvarande efter en motiverad In Vivo Labbtekniker för det växande teamet i Mölndal. I den här rollen kommer du att ge direkt stöd till forskarna som arbetar i djuranläggningarna genom att samla in och beställa laboratoriematerial, fylla på laboratoriematerial, upprätthålla en ren arbetsmiljö och mycket mer!Är du intresserad av att arbeta i en internationell miljö med många kontakter där du kan leverera den högsta servicenivån till kunden? Är du kundorienterad och mycket motiverad? Då kan detta vara en möjlighet för dig! Är du intresserad? – Låt oss diskutera!
Kanske arbetar du för närvarande inom logistik, tjänster eller försäljning och har ett allmänt intresse för vetenskap, så då är detta din möjlighet att bli en del av en labbmiljö!
Denna roll är på heltid och är en permanent position baserad hos vår kund, med placering i Mölndal. Utöver en attraktiv lön erbjuder vi flera förmåner såsom bonusplan, pensionssystem och friskvårdsbidrag.
Arbetstider: Måndag - fredag, starttid mellan 6:00 - 9:00 och sluttid 15:00 - 18:00


Teamet
Detta är ett nyskapat team som är under tillväxt. Hittills består teamet av en In Vivo Lab Manager och en In Vivo-tekniker. Tillsammans tillhör de vår avdelning Lab & Production Services, som hjälper stora läkemedelsföretag och laboratorier över hela världen med forskning och utveckling inom Life Sciences-industrin.


Erfarenhet som krävs
Utbildning: Gymnasieexamen, öreträdesvis med anknytning till djurhantering
Erfarenhet:
med någon typ av djurarbete är en stor tillgång
i laboratoriemiljö är ett plus, men inte ett krav

Erforderliga färdigheter:
Goda kunskaper i MS Office
Flytande i både svenska och bra i engelska
Nyfiken, anpassningsbar och självständig
Serviceminded, utåtriktad och hårt arbetande
Bekväm med att arbeta i ett djurlaboratorium



Huvudsakliga uppgifter och ansvarsområden
Stöd vid diskning och skötsel av labbglas och labbtillbehör, inklusive djurburar
Insamling, inköp och påfyllning av förbrukningsmaterial, t.ex. labbrockar och kemikalier
Förbereda varor för in- och utpassering i slutna utrymmen
Inköp och påfyllning av djurrelaterade produkter för daglig användning, t.ex. mat
Underhålla arbetsområdet
Bidra till att skapa, underhålla och uppdatera relevanta document



LI-Onsite Visa mindre

Do you have expertise in mathematical modelling and/or pharmacokinetics and pharmacodynamics? Would you like to apply your knowledge in a global company that follows the science and turns ideas into life-changing medicines? Then you could be the new colleague we are looking for to be part of the development of future treatment within respiratory and immunology.
Our team is growing, and we now have two openings for highly skilled and passionate scientists with expertise in mathematical modelling, preferably applied in the field of pharmacokinetics-pharmacodynamics (PKPD), to join the Drug Metabolism and Pharmacokinetics (DMPK) team of project leads within the Early Respiratory and Immunology (R&I) therapeutic area at AstraZeneca in Gothenburg, Sweden. Working at AstraZeneca means being entrepreneurial, thinking big and working together to make the impossible a reality.
Early R&I is one of the three main therapeutic research areas within AstraZeneca which deliver candidate drugs into late-stage clinical development. DMPK interacts with other functions in supporting Early R&I projects all along the value chain, from target selection all the way to market launch and life-cycle management. At AstraZeneca we are proud to have an outstanding workplace culture that encourages innovation and teamwork. We are united by our vision to push the boundaries of DMPK science to transform ideas into medicines for R&I patients. Employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity toward delivering candidate drugs into late-stage development.
What you’ll do?
You have a true passion for science and will support our portfolio within the R&I therapeutic area. We believe that you have solid, hands-on experience of PKPD modeling and that you will be able to provide expert advice and interpretation of complex drug discovery data. You will deliver translational quantitative/PKPD input for a broad range of drug modalities from target identification to life-cycle management.
Main Duties and Responsibilities include:
Identify the appropriate mathematical modelling approach (e.g. traditional PKPD modelling, non-linear mixed effects modelling, quantitative systems pharmacology) to deliver a translational quantitative PKPD strategy in projects, so that effective conclusions can be made
Inform and influence the design of studies, with PKPD in mind to answer relevant pharmacological questions and report results and interpretations to project teams and internal governance bodies
Design preclinical PKPD studies, contribute to estimation of safety margins and report results and interpretations to project teams and internal governance bodies
Integrate the appropriate data to predict human pharmacokinetics, efficacious human drug exposure, human longitudinal response (e.g. biomarker and disease effects), and human dosing regimen. This is done in close collaboration with other functions (biologists, safety scientists, clinical pharmacologist and clinical pharmacometricians)
Communicate scientific progress to internal and external stakeholders

Depending on your background, experience and skills, your initial career level will be a Senior Scientist, Associate Principal Scientist or Principal Scientist.
Essential for the role
The successful candidate is expected to have a solid PKPD understanding and hands on experience of mathematical modelling (e.g. empirical PKPD models, in vitro-in vivo translation, non-linear mixed effects models, quantitative systems pharmacology (QSP) models).
PhD or equivalent in relevant field, with a focus on mathematical modelling of PKPD data, ideally in a preclinical/translational setting
Hands-on experience with modelling software (e.g. Phoenix WinNonlin, Matlab, Monolix, R, NONMEM, or similar)
Proven scientific leadership and ability to mentor junior colleagues
Experience in project leadership and collaborative mindset
Scientific leadership evidenced by a publication track record and ability to independently lead the drafting and review of publication manuscripts
Excellent interpersonal skills, and ability to work in cross-functional teams as well as independently
Proactive and excellent communication skills

Why AstraZeneca?
At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.
Work policy
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
What’s next?
This is an exciting opportunity for a talented modeller to join a strong team and support the portfolio of a major pharmaceutical company that has science at its heart whilst being based in the wonderful city of Gothenburg, Sweden. If you are ready to make a difference - apply today, and we'll make it happen together!
We welcome your application until 2024-06-16 Visa mindre

Job description
Are you a motivated cell biologist with experience of in vitro work in molecular biology, omics and oligonucleotides? Do you also enjoy working hands-on in the lab with a great group of colleagues by your side? If yes, this might be the next position for you!
Right now, we are looking for a highly engaged and enthusiastic cell biologist to join as a Discovery Safety Scientist and complement us in our In Vitro Safety group at AstraZeneca in Gothenburg, Sweden. The ideal candidate will have a passion for in vitro lab based experimentation and analysis and value the utility of early drug safety investigations. We are looking for someone with strong communication and collaboration drive, who can adopt a brave and forward-thinking approach to drive our predictive in vitro safety assay design to support drug discovery and development projects.
Why AstraZeneca?
We are working towards treating, preventing, modifying and even curing some of the world’s most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthrough come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.
Does this sound like your next challenge? Apply today!
This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.
Deadline: 2024-06-11 selection and interviews will be ongoing. For more information: Please contact Malin Fridholm, [email protected]





Responsibilities
What you’ll do:
Working in an industry-leading in vitro safety lab you will work with internal research groups to identify potential off-target risks for siRNA/antisense oligonucleotide (ASO) projects. Develop in vitro assays to explore those potential off targets in a variety of different mammalian cell types via gene expression analysis. You will also be required to summarize safety related literature relating to modulation of off-target genes to help inform decisions and support the development of safer oligonucleotide-based drug products.

Qualifications
Essential for the role:
PhD in biology, biotechnology, toxicology or pharmacology or a related field.
Strong background in mammalian cell biology and in vitro work in molecular biology & omics including gene expression modulation via siRNA/ASOs and qPCR measurements. Additional in vitro techniques would be advantageous including fluidigm qPCR, high content cell imaging, western blot, ELISA & FACs.
Experience of complex in vitro cell models or MPS systems would be desirable.
Track record of scientific literature review with an ability to pull together various sources of data to inform on potential safety questions & targets of interest.
Strong communication skills: including presenting, communicating data analysis, influencing and building partnerships with internal and external research groups.


About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
We are currently looking for a laboratory skilled Scientist to join the Bioscience COPD IPF Department within Early Respiratory and Immunology (R&I). This role is located in Gothenburg, Sweden.
The Bioscience COPD/IPF department consist of 7 teams spread across Sweden, UK and US and our focus is primarily to progress projects within our portfolio, but it also includes work to increase our knowledge of COPD and IPF and to support target identification for new projects.
What you´ll do:
As a Scientist you will plan, optimise, and execute in vitro experiments as well as support analysis from both in vitro and in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You are expected to actively take part in scientific discussions and to add valuable input in experiment design and data interpretation to drive projects and techniques.
This is a lab-based role where you will be involved in multiple ongoing projects with responsibility to perform experiments from various cells and tissues for both in vitro-, in vivo- and patient studies. This role will give the opportunity to support, design, develop and conduct experiments supporting the identification of new drug targets and the progression of drug discovery projects.
For this role, we are looking for someone with experience in modern cell biology and molecular analysis techniques that rapidly can become an integrated project member and deliver key data.
AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.
This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.
About randstad life sciences
Randstad Life Sciences is specialized in competencies within Life Science. As a consultant with us, you get a competitive salary, benefits, and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many activities.
Deadline: 2024-06-10, selection and interviews will be ongoing. For more information please contact Malin Fridholm at [email protected]



Responsibilities
We will rely on you to:
Execute in vitro/ex vivo experiments according to study plans
Contribute to the interpretation of experimental data and play an important role in the planning of further experiments
Effectively communicate results to other members of the project, team or to departments as required. Be an effective team member in supporting projects to meet their objectives
To conduct where appropriate in parallel more than one area of work to agreed timelines
Possess a range of practical skills and demonstrate flexibility within and across teams


Qualifications
Essential requirements:
A relevant science degree (MSc or BSc) ( e.g Molecular/Cell Biology, Pharmacy, Biotechnology)
Practical experience running in vitro assays and cell culturing
Relevant experimental experience in cell and molecular biology methods, immunoassays, protein and RNA analysis
Isolation, culturing and analysis of primary cell cultures along with experience in the use of biological dose response assays is desirable. Experience in immunological methods (ELISA, MSD), protein analysis (western blot) and RNA analysis (qPCR) plus handling and evaluation of pharmacological drug substances would also be benificial.
Excellent written and oral communication skills in English is a must
Soft skills:

You also possess great problem-solving skills. You have a positive and goal-oriented attitude, and you are a team player but are also able to take your own initiatives. You are organized and incorporate the views of others in your communication and collaboration.

About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.
With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.


We are currently looking for a laboratory skilled Scientist to join the Bioscience COPD IPF Department within Early Respiratory and Immunology (R&I). This role is located in Gothenburg, Sweden.
The Bioscience COPD/IPF department consist of 7 teams spread across Sweden, UK and US and our focus is primarily to progress projects within our portfolio, but it also includes work to increase our knowledge of COPD and IPF and to support target identification for new projects.


This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities
What you´ll do:
As a Senior Scientist you will plan, optimise, and execute in vitro experiments as well as support analysis from both in vitro and in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You are expected to actively take part in scientific discussions and to add valuable input in experiment design and data interpretation to drive projects and techniques.
This is a lab-based role where you will be involved in multiple ongoing projects with responsibility to perform experiments from various cells and tissues for both in vitro-, in vivo- and patient studies. This role will give the opportunity to support, design, develop and conduct experiments supporting the identification of new drug targets and the progression of drug discovery projects.
For this role, we are looking for someone with experience in modern cell biology and molecular analysis techniques that rapidly can become an integrated project member and deliver key data.
We will rely on you to:
• Execute in vitro/ex vivo experiments according to study plans
• Contribute to the interpretation of experimental data and play an important role in the planning of further experiments
• Effectively communicate results to other members of the project, team or to departments as required
• Be an effective team member in supporting projects to meet their objectives
• To conduct where appropriate in parallel more than one area of work to agreed timelines
• Possess a range of practical skills and demonstrate flexibility within and across teams


About randstad life sciences
Randstad Life Sciences is specialized in competencies within Life Science. As a consultant with us, you get a competitive salary, benefits, and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many activities.


Deadline: 2024-06-06, selection and interviews will be ongoing. For more information: Please contact Katan Ali, [email protected]

Qualifications
Essential requirements:
Essential for the role (requirements for the matrix in FG):
-A relevant science degree (PhD) ( e.g Molecular/Cell Biology, Pharmacy, Biotechnology)
-Practical experience running in vitro assays and cell culturing
-Relevant experimental experience in cell and molecular biology methods, immunoassays, protein and RNA analysis
-Isolation, culturing and analysis of primary cell cultures along with experience in the use of biological dose response assays is desirable. Experience in immunological methods (ELISA, MSD), protein analysis (western blot) and RNA analysis (qPCR) plus handling and evaluation of pharmacological drug substances would also be benificial.
Experience in lung research is desirible
- Excellent written and oral communication skills in English is a must


Soft skills (not for Matrix but good to know when interviewing):
You also possess great problem-solving skills. You have a positive and goal-oriented attitude, and you are a team player but are also able to take your own initiatives. You are organized and incorporate the views of others in your communication and collaboration.


AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Job description
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives- and are made to feel valued, energized and rewarded for their ideas and creativity. In AstraZeneca we set pride to drive the development in a sustainable way, in all areas of our business from influencing our suppliers through development to commercial products.


The arena:
We now have the opportunity for one or several consultants to join our team in the role as Formulation Scientist/Product Developer within the department Oral Product Development at AstraZeneca in Gothenburg. The assignment is on a temporary basis.


Tasks and responsibilities/The role:
We are looking for a formulation scientist who can work together with us with generating and evaluating pharmaceutical technologies and formulations. The work includes development, characterization, and documentation, mainly of solid based formulations, in order to develop drug products.


The tasks include planning and implementation of experiments with the aim of generating new formulations and optimizing processes in lab and pilot scale. We are looking for both people with and without previous experience in the area.


This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.


About randstad life sciences
Randstad Life Sciences is specialized in competencies within Life Science. As a consultant with us, you get a competitive salary, benefits, and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many activities.


Deadline: 2024-05-23, selection and interviews will be ongoing. For more information please contact Malin Fridholm at [email protected]

Responsibilities
We are looking for a formulation scientist who can work together with us with generating and evaluating pharmaceutical technologies and formulations. The work includes development, characterization, and documentation, mainly of solid based formulations, in order to develop drug products.


The tasks include planning and implementation of experiments with the aim of generating new formulations and optimizing processes in lab and pilot scale. We are looking for both people with and without previous experience in the area.

Qualifications
Essential/desirable for the role:
MSc/BSc in chemistry, pharmacy, chemical engineering, food technology or equivalent. Good knowledge in written and spoken Swedish and/or English is necessary as well as laboratory experience including working with computerized systems. If you have experience from working within the pharmaceutical industry, medical tech, or with manufacturing equipment, this will be an advantage. Solid materials/formulation experience is highly meriting.


As a person, you should be well organized, analytical, flexible and accurate. Good team working skills are also important, together with the ability to operate independently. Good communication skills linked to the ability to work to tight timelines are highly valued.


AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

About the company

Randstad
At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential. With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward. Visa mindre

Are you a highly skilled and collaborative in vitro scientist? Would you like to develop assays and run experiments to qualify candidates for our rapidly developing siRNA portfolio? Are you eager to work with super nice colleagues to deliver impactful data and be an integral part in our streamlined organizational structure with short decision routes? If yes, please read further!
About usRibocure Pharmaceuticals AB (Ribocure) is an international R&D Centre based at GoCo in Gothenburg, and is a subsidiary of Suzhou Ribo Life Science Co., Ltd. (Ribo).
Ribo was established in 2007 in China and is a company with a vertically integrated cutting-edge RNAi technology including patented GalNAc liver-targeting technology -Ribo-GalSTARTM, oligonucleotide design, screen, preclinical proof of concept and clinical testing as well as large scale CMC capacity.
Ribocure was established in Jan 2022 in Gothenburg and represents Ribos commitment to globalize its technology and develop life-saving therapies. Ribocure has a Ph2 clinical trial unit and an in vitro lab integrated in our HQ located in GoCo area in Mölndal, Sweden. The clinical trial unit is dedicated to run innovative clinical trials with the focus on rare disease indications to address unmet medical need. (www.ribocure.com)
The role
We are currently seeking a motivated, skilled and experiencedIn vitro Lab Scientistto help drive the development of our siRNA therapeutics. The scientist will be responsible for conducting advanced cell culture work, including IPS derived cell and organoid models, and molecular analysis of protein and mRNA expression. Experience working with siRNA is highly meriting.
Responsibilities: Conduct cell culture experiments (primary, cell lines and pluripotent stem cells)
Support in vitro screen in primary cells
Set up organoid models to create complex tissue structures in vitro
Analyze protein and mRNA expression
Maintain accurate records of experiments and data reports
Participate in lab meetings, present research findings, and contribute to scientific discussions
Keep up-to-date with current literature in the field and implement new techniques and methods as necessary


Requirements: PhD or MS in Biology, Biochemistry, or related field
A minimum of 2 years experience from Pharma Industry anddrug development
Extensive experience with cell culture techniques
Experience with IPS derived cell work and organoid models
Experience of imaging techniques and analysis
Proficiency in molecular analysis of protein and mRNA expression
Ability to work independently and as part of a team
Excellent communication and organizational skills
Attention to detail and ability to maintain accurate records of experiments and findings
Ability to multitask and manage multiple projects simultaneously
What we offer
We offercompetitive salary, comprehensive benefits packageand opportunities for advancement. We are an equal opportunity employer and welcome applicants from all backgrounds. We also offer you opportunities to grow with our fast-expanding global organization towards being one of the leading players in oligonucleotide therapeutics.
Come join us at Ribocure and help shape the future of medicine!
Send your application by clicking Send Application.
Should you have any further questions regarding the position, please do not hesitate contacting Dr Johannes Wikström.
Welcome!
This recruitment is quality assured by HR On Demand. Visa mindre

Nyctea, founded in 2020, is a biotech company on a mission to create affordable medicine. A key to succeeding is to improve the purification process which today accounts for 60-80% of the total manufacturing cost. Based on inventions and research from Chalmers University of Technology we are commercializing a new material that enables electrification and digitalization of the purification process enabling sustainable and cost-effective purification of biopharmaceuticals. Our team today consists of 5 FTEs and we have recently begun selling our product to the pharmaceutical industry. We are looking for a Biotechnology Engineer to contribute to the development, production and distribution of our product. Our next milestones are to sell and deliver projects with pharma companies, develop and launch products. To do so we need to scale-up of manufacturing volumes, as well as improve the capability and capacity of our product, while also working towards satisfying industry standards such as ISO and good manufacturing practices (GMP).
Responsibilities:
1. Product testing: Lead internal technical efforts in evaluating performance of products.
2. Product development: Collaborate on projects to improve existing functions and to develop new functionalities and features of products and related problem solving.
3. Product delivery installation and deployment: Participate in the technical sales process to be an interface with customers in providing technical support on-site and/or remotely to ensure satisfactory performance of the product.
4. Communication: Prepare technical reports, document research for intellectual property purposes, and assist in writing patent applications.
5. Quality assurance: Lead efforts in establishing a quality management system for our manufacturing process.
Qualifications:
1. Education: M. Sc in Biotechnology or on-going studies in Biotechnology is a requirement.
2. Work experience: Expertise in practical biotechnology and bioprocess laboratory work such as chromatography, electrophoresis, working with cell cultures, western blots etc is a requirement. Additionally having experience in analytical chemistry and surface characterization methods such as UV-vis spectroscopy, SPR, NMR, electrochemistry is a merit. Experience in working with novel purification methods of biomolecules using electrochemistry is a merit.
3. Communication: Excellent communication skills in English, both written and spoken. Proficiency in documenting laboratory procedures and results.
4. Startup experience: Experience in working on early-stage research, in research groups and in startups is a merit.
5. Extensive Network: Well-established industrial and academic network. Visa mindre

Brinner du för miljö- och hållbarhetsfrågor? Är du nyfiken, driven och initiativrik och vill arbeta tillsammans med partners och kunder mot ett hållbart samhälle?

Vår enhet Miljö och hållbar kemi expanderar inom livscykelanalysområdet och vi söker nu en medarbetare med erfarenhet av livscykelperspektivet för att bli en del av vårt team.

Den person vi söker bör ha kunskap inom området batterier och/eller metall/mineral. I vår verksamhet, lokaliserad i Mölndal och Stockholm, arbetar vi med frågor inom områdena cirkulär ekonomi, resurseffektivitet, livscykelanalys och hållbarhetsbedömning. Enheten är även hemvist för Substitutionscentrum och Kemikaliegruppen på RISE.

Om rollen
I din roll hos oss kommer du att arbeta med livscykelperspektiv och livscykelanalys i större projekt såväl som i direkta uppdrag mot kund. Vi arbetar mycket i team, men vi värdesätter även högt förmågan att ta egna initiativ och arbeta självständigt då en viktig del av vår verksamhet involverar initiering och ledning av projekt som svarar mot industrins behov. Som medarbetare på RISE har du stora möjligheter att forma dina arbetsuppgifter och bidra till ett hållbart samhälle, via uppdrag, men även i anslagsfinansierade projekt både nationellt och på EU-nivå.

Du kommer att medverka som LCA-expert och utförare i våra projekt och kommer även att leda och driva projekt mot kund samt medverka vid försäljning av projekt. Du arbetar tillsammans med kompetenta medarbetare inom enheten och övriga RISE, både i kortare uppdrag och i projekt som löper under ett antal år. 

Viktiga arbetsuppgifter är:

- Kontakt med kunder, samarbetspartners och finansiärer
- Projektledning och initiering av nya projekt och uppdrag
- Livscykelanalys där datainsamling, modellering, beräkning och analys avseende miljöpåverkan ingår, och även att vägleda kunden i att använda resultaten för produkt- eller processförbättringar
- Bygga internt och externt nätverk.

Befattningen är eller kan komma att bli placerad i säkerhetsklass, vilket innebär att säkerhetsprövning kan komma att ske i enlighet med säkerhetsskyddslagen. Placering för tjänsten är Mölndal eller Stockholm.

Vem är du?
Vi söker dig som har ett stort intresse för miljö- och hållbarhetsfrågor och flerårig erfarenhet av arbete med livscykelanalys. Du har relevant akademisk utbildning och erfarenhet av att genomföra LCA och använda relevant mjukvara såsom SimaPro, GaBi eller OpenLCA. För att lyckas i din roll ser vi att du har god erfarenhet inom miljöbedömning, det kan handla om livscykelanalyser, miljövarudeklarationer (EPD), klimatfotavtryck och miljöutredningar utifrån ett livscykelperspektiv, men även att bidra med beslutsunderlag avseende produkt- och processförbättringar.

Som person är du kundfokuserad och kommunikativ, och kan uttrycka dig väl i både tal och skrift på både svenska och engelska. Du tycker om att skapa nätverk, ser möjligheter och arbetar för att bidra till enhetens projekt- och uppdragsportfölj. Du är initiativrik och driven med god förmåga att arbeta självständigt såväl som i team. Forskarutbildning såväl som kemikompetens är meriterande.

Är vi rätt för varandra?
Inom RISE gillar vi olika och vi är övertygade om att mångfald bidrar till en innovativ miljö där vi tillsammans utmanar gränser och utvecklar ny kunskap och kompetens för framtiden. Hos oss möts passionerade problemlösare för att lösa några av världens viktigaste, och kanske roligaste, problem. Vi kan inte lova dig ett enkelt jobb, men vad vi kan lova dig är ett gäng engagerade kollegor och några riktigt spännande samhällsutmaningar att ta itu med. Du kommer att arbeta i en dynamisk miljö som ger dig utvecklingsmöjligheter både professionellt och personligt. Hos oss får du möjlighet att göra skillnad på riktigt. Välkommen till hela Sveriges forskningsinstitut och innovationspartner.

Kontakt
Välkommen med din ansökan senast den 12 april. Vid frågor om tjänsten, kontakta enhetschef Lisa Schwarz Bour, tel: 010-228 48 07.

Våra fackliga representanter är Lazaros Tsantaridis, Sveriges Ingenjörer (SACO), +46 10-228 41 22 och Bertil Svensson, Unionen, +46 10-516 53 56.

Vi har valt rekryteringskanaler för den här anställningen och vill inte bli kontaktade av rekryteringsföretag.

Livscykelanalys, hållbarhet, cirkulär ekonomi, batterier, innovationskritiska metaller och mineral,resurseffektivitet, projektledning, miljö, RISE, Mölndal, Stockholm Visa mindre

Scantox Sweden är ett kontraktslabb inom läkemedelsutveckling, på labbet i Mölndal är vi specialister på organisk analytisk kemi. Vår verksamhet bygger på utveckling av analysmetodik utefter enskilda kunders specifika behov samt att utföra kvalitetskontroller för frisläppning till marknaden. Hos oss får du en varierad arbetsdag med påverkansmöjlighet och beslutsansvar för ditt arbete. Kunderna är primärt producenter och importörer av läkemedel & medicintekniska produkter, men även helt andra fält som livsmedel och miljöprover behandlas. Detta i kombination med vår breda instrumentpark med tonvikt på kromatografi och masspektrometri ger möjlighet att lära sig nya tekniker och utvecklas inom fältet organisk analytisk kemi.
Scantox söker dig med universitetsutbildning med inriktning kemi och kvalitet. Du bör ha åtminstone ett par års arbetslivserfarenhet från arbete i den privata sektorn/industrin med analyser under GMP eller ackreditering (ex.vis. ISO17025), endast akademisk erfarenhet är av mindre intresse. Det är viktigt att du beskriver dina erfarenheter av GMP-analyser i din ansökan.
Flera kritiska instruktioner är på svenska så du bör behärska språket och din ansökan skall skrivas på svenska.
I rollen som analytisk kemist utför du kvalitetskontroll av medicintekniska produkter samt läkemedelsprodukter. Du arbetar laborativt enligt upprättade rutiner och ansvarar för att utvärdera och rapportera resultat i LIMS-system. Du måste ha erfarenhet av att självständigt analysera prover med ex.vis. UPLC/HPLC och bedömma resultaten. Har du också erfarenhet av Dissolution-analyser är detta mycket meriterande.
Vi söker dig som är ansvarstagande och har ett noggrant och strukturerat arbetssätt. Arbetet är varierat då vi har många olika produkter för frisläppningsanalys och möjlighet att utvecklas inom många olika analystekniker finns.
Arbetet är heltidsanställning med fast lön. Tjänsten är placerad i Mölndal. Vi har ingen möjlighet att hjälpa till med boende så sökanden med boende inom pendlingsavstånd är meriterande.
Ansökan sker senast 2 april 2024 genom att skicka CV och personligt brev till [email protected]. Urval och intervjuer kommer att ske efter sista ansökningsdag. Kandidater som skickar in underlag godkänner att dessa behandlas under processen. Uppgifterna kommer att raderas senast 6 månader efter att rekryteringen avslutats.
Frågor kan ställas till Rickard Wahlström (Site manager) alternativt Johanna Lindvall (Operational manager), på [email protected] eller 031-24 22 00. Visa mindre

Job description
nalytical Chemists (Scientist or Senior Scientist) – Early Product Development and Manufacturing, AstraZeneca Gothenburg


At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.


Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be “pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future”.
We’re looking for talented and motivated analytical chemist to join one of our analytical characterization teams within Early Product Development and Manufacturing (EPDM) in Gothenburg.


This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.

Responsibilities
You would join a highly collaborative team and together we will deliver the analytical science to product development within the early portfolio up to phase II.
To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully and to the right quality. You will get the opportunity to apply your excellent analytical expertise to the drug projects you are working in, contributing to the progression of these projects and drive the scientific development within the field of analytical science at AstraZeneca.


About randstad life sciences
Randstad Life Sciences is specialized in competencies within Life Science. As a consultant with us, you get a competitive salary, benefits, and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many activities.


Deadline: 2024-03-22, selection and interviews will be ongoing. For more information: Please contact Katan Ali, [email protected]

Qualifications
Required Qualifications, Skills and Experience:
-University degree (MSc, PhD) in relevant discipline, preferable with industry experience
-Scientific knowledge within analytical science and technically skilled to use chromatography with relevant detection techniques for small molecules
-You are a driven experimentalist, with a passion to deliver highly relevant and reliable data and with the ability to be influential in discussions in a wide set of communities and multi-disciplinary project teams
-Excellent communication, collaboration, networking and leadership skills & ability to lead and inspire colleagues
 
If you also have experience in one or more of the following areas – great!
-Industry experience of pharmaceutical development including oral solid dosage form development
-Experience of CMC submissions and work according to GMP
-Skilled in specific analytical techniques for small molecules, e.g. mass spectrometry, NMR, dissolution etc
-Track record and keen interest of driving development within analytical science including championing new technologies and solutions


AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

About the company

Kelly Services (UK) Limited Visa mindre

Vetenskaplig utbildning krävs inte för det här jobbet, du kommer att få full utbildning internt!
Avantor letar för närvarande efter en motiverad In Vivo tekniker för det växande teamet i Mölndal. I den här rollen kommer du att ge direkt stöd till forskarna som arbetar i djuranläggningarna genom att samla in och beställa laboratoriematerial, fylla på laboratoriematerial, upprätthålla en ren arbetsmiljö och mycket mer!
Är du intresserad av att arbeta i en internationell miljö med många kontakter där du kan leverera den högsta servicenivån till kunden? Är du kundorienterad och mycket motiverad? Då kan detta vara en möjlighet för dig! Är du intresserad? – Låt oss diskutera!
Denna roll är på heltid och är en permanent position baserad hos vår kund, med placering i Mölndal. Du kommer att arbeta från måndag till fredag, med flexibla arbetstider och inget skiftarbete. Utöver en attraktiv lön erbjuder vi flera förmåner såsom bonusplan, pensionssystem och friskvårdsbidrag.
Teamet
Detta är ett nyskapat team som är under tillväxt. Hittills består teamet av en In Vivo Lab Manager och en In Vivo-tekniker. Tillsammans tillhör de vår avdelning Lab & Product Services, som hjälper stora läkemedelsföretag och laboratorier över hela världen med forskning och utveckling inom Life Sciences-industrin.
Erfarenhet som krävs
Laboratorieerfarenhet, helst inom djuranläggningar eller produktion, är önskvärd
Erfarenhet av arbete inom djurrelaterade lab är meriterande
Goda kunskaper i MS Office
Flytande i både engelska och svenska
Samarbetsvillig, en stark lagspelare och självständig
Serviceminded, utåtriktad och praktiskt lagd
Bekväm med att arbeta i ett djurlaboratorium

Huvudsakliga uppgifter och ansvarsområden
Kartlägga dagliga aktiviteter för att skapa en standard för framtiden, eftersom detta är ett växande team
Hantera laboratoriematerial
Samla in, hantera och köpa in laboratoriekläder, t.ex. operationsrockar och rockar
Fylla på förbrukningsmaterial och kemikalier och se till att allt finns tillgängligt för forskarna hela tiden
Fylla på material, berikningsmaterial och foder för djur
Påfyllning av gas, torris och flytande kväve
Hålla arbetsområden rena, visst underhåll
Bidra till att skapa, underhålla och uppdatera relevant dokumentation



LI-EUR Visa mindre