Lediga jobb Randstad i Mölndal

Job description
Do you have experience within analytical and biophysical characterization of biomolecules and enjoy working in the lab? Are you interested in working with a broad array of molecules and analytical techniques in the pharmaceutical product development area? We are looking for you that are an analytical chemist with experience of biomolecule characterization and working according to Good Manufacturing Practice (GMP).

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
 
AstraZeneca is now seeking two Analytical Scientists to join their New Modality CMC Analytics team within the Advanced Drug Delivery (ADD) function that is part of Pharmaceutical Sciences at AstraZeneca in Gothenburg, Sweden.
 
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. Our portfolio of projects spans traditional small molecules, peptides, oligonucleotides to RNA based therapeutics across AstraZeneca’s therapy areas. Advanced Drug Delivery (ADD) resides within Pharmaceutical Sciences with a mission to provide novel products to AstraZeneca’s clinical pipeline.

Responsibilities
As a Scientist working in the clinical development phase within ADD you will support drug projects from an analytical perspective, from candidate drug nomination over Phase 2 clinical trials. You will focus on characterization of various molecules, primarily oligonucleotides, using several different analytical techniques. The role covers development and validation of analytical methods, stability studies, release analysis, and other type of analytical support to drug projects. Part of the work is performed according to GMP. You will work as a member of cross-functional pharmaceutical project teams and in close collaboration with other analysts, formulators, chemists and biologists at AstraZeneca in Sweden, UK and US.
 
Preferably, you should be experienced in analytical and biophysical characterization of biomolecules as well as working in pharmaceutical development, including working according to GMP. You should possess an enthusiasm for laboratory-based work, be flexible and have a problem-solving mind-set. 


 
Main Duties and Responsibilities
Give analytical support to drug development projects, such as stability studies, release analysis and other supportive characterization experiments, using techniques like UV spectrophotometry, LC-UV/MS and liquid particle counting.
Development and validation of analytical methods.
Generate, evaluate and report data clearly and reliably. 
Prepare documentation and formal reports in accordance with current standard procedures and where appropriate, according to GMP standard. 
Give analytical support to scientific initiatives on new technologies/processes together with specialists and/or technology networks. 
Working as a member of cross-functional drug development project teams.


Qualifications
Essential Requirements
MSc degree in a relevant scientific discipline (e.g., Analytical Chemistry, Biochemistry or Biotechnology).
In-depth knowledge of analytical methodologies such as chromatography, mass spectrometry and biophysical characterization techniques.
Thorough understanding of principles and applications of Good Manufacturing and Laboratory Practices (GMP/GLP).
Ability to communicate in English both orally and in writing.

 
Desirable Requirements
3+ years of industrial experience of analytical work with biomolecules in clinical drug development phase.
Qualified to execute analytical work according to GMP.
An interest in exploratory analytical work related to complex molecules and new technologies.


For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-03-01, selection and interviews will be ongoing. The position may be filled before the last day.
For more information:  Eleonor Ehrman, consultant manager,  +4673-343 41 09 or Kerstin Karlsson, consultant manager, [email protected].

About the company
 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.

Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Job description
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. 


Inhalation Product Development (IPD) at AstraZeneca is a multinational organization that combines decades of experience in inhalation technology whether it is nebulization, pMDI or DPI. Our vision is to develop and provide to patients best-in-class, innovative and sustainable products to deliver medicine via inhalation.

Responsibilities
We’re looking for a talented and motivated Analytical Scientist to join our Analytical Sciences team working with characterization of small inhaled molecules within IPD in Gothenburg.
You would join a highly collaborative team and help us deliver the analytical science to progress product development. 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. This is a consultant assignment where 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.

Qualifications
University degree (MSc) in relevant discipline, with 1-2 years industry experience
Scientific knowledge within analytical science and technically skilled to use chromatography and detection of small molecules
Experience in characterization techniques used for inhaled products, such as impactor analysis
Experience with method development and validation 
Experience from working and communicating within a global project environment
Experience with solving technical challenges and problems 
Experience of work according to GLS
Experience of working in a GMP environment
Strong ambition to develop yourself and others

For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-02-28, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.
For more information: Kerstin Karlsson [email protected] or Eleonor Ehrman +46733434109. 

About the company
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.

Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Job description
At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe.

As a Senior Research Scientist in cellular assay development in Gothenburg, Sweden, you’ll play a pivotal role in channelling our scientific capabilities to make a positive impact on changing patients’ lives. You will work within Discovery Sciences, part of AstraZeneca’s BioPharmaceuticals organisation, which focuses on scientific advances in established and emerging medicine formats and drug discovery technologies across therapeutic areas including, respiratory and inflammation (RIA), cardiovascular and metabolism (CVRM).

We have an exciting opportunity for you to join Discovery Sciences’ Discovery Biology Department as a lab-based scientist in the Cellular Assays Team developing state-of-the-art cell-based screening assays and detailed biological mechanism-of-action studies to support projects in all phases of AstraZeneca’s drug discovery pipeline with a significant focus in RIA and CVRM disease areas.

Specifically, the successful candidate will take a lead scientific role in applying their skills using imaging technologies and developing high content assays.

Responsibilities
 Lab-based scientist utilizing expertise in cellular assay development; independently designing, developing and validating assays for implementation in drug discovery projects, while incorporating the views of others
 Work in partnership with colleagues in the High Throughput Screening and Mechanistic Biology & Profiling teams and across the organisation 
 Design and implement work-plans to agreed timelines to meet project objectives, including delivery of more than one agreed area of work in parallel
 Be an effective member of Drug Discovery Project Teams, contributing novel ideas and using judgement and knowledge to influence the work of the project
 May lead one or more aspects of scientific discipline within the team
 Maintain an awareness of current developments in the literature and contribute to the continuous capability enhancement process by identifying opportunities where improvements can be made
 Achieve personal scientific visibility through project contributions and internal presentations at departmental or functional meetings; and external scientific visibility through poster and oral conference presentations and authorship on peer-reviewed publications


Qualifications
Essential Requirements
 PhD in Biology, Pharmacology, Cell biology or a related discipline or a BSc/MSc degree with significant relevant experience, preferably in the pharmaceutical or biotechnology industry
 Strong experience in cellular biology techniques applied to development of physiologically relevant cellular assays 
 Expertise in the design, development and validation of cellular imaging assays for compound profiling
 Experience in advanced and automated fluorescent based imaging platforms
 Experience in use and development of scripts for quantitative image analysis  


Desirable Requirements
 A practical understanding of a wide range of cellular assay methods and technologies (e.g., fluorescence, luminescence, target engagement techniques, plate-based automation) as applied to a range of biological targets for compound profiling and screening
 Good publication records in peer-reviewed journals preferably in the field of RNA degradation biology
 Excellent problem-solving skills, strong delivery focus and communication skills
 Research experience in RIA and/or CVRM diseases
 Excellent team working and networking skills with experience of interacting effectively across interfaces of discipline, culture, and expertise

For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-03-05, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.
For more information: Kerstin Karlsson [email protected] or Eleonor Ehrman +46733434109. 

About the company
Randstad Life Sciences specializes in the field of science and is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Job description
Master student project on PROTACs assay development at AstraZeneca, 60 credits
 
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.
 
Introduction 
We have an attractive opening for a master student to join our In vitro Biochemical Assays team, for developing high throughput assays for studying PROTAC-mediated protein degradation. PROTACs (Proteolysis targeting chimera) have emerged as an important new modality in drug discovery with the potential to deliver the next generation of medcines. We are interested to explore novel in vitro assays for understanding the mechanism of PROTAC-mediated protein degradation. 
 
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. Our Discovery Sciences team operates from truly state-of-the-art centre in Sweden. You’ll work with some of the most knowledgeable technological experts in the industry, all collaborating on high-profile drug discovery projects. We’re also early adopters of new technologies to support innovation, including CRISPR, genome editing techniques, PROTACs, transcriptomics and next-generation sequencing.

Responsibilities
On a daily basis you will work in the In vitro Biochemical Assays team with colleges/experts working on developing high throughput biochemical assays using state-of-the-art technologies to support drug discovery projects. You will be developing a project integrated in our current research activities benefiting from daily support from an experienced supervisor. 
 
In this project you will learn about the new concept of PROTAC (Proteolysis targeting chimera) modality of medicine, and have the opportunity to explore world-leading science and develop different in vitro high throughput assays for studying the mechanism of PROTAC-mediated protein degradation. During this period you will gain extensive experience in developing high throughput in vitro  assays to study the mechanism of PROTACs. You will gain practical independency in techniques/skills such as experimental design, cell culturing, Western blotting, advanced assay technologies such as TR-FRET, NanoBBRET and Nano-Glo assays, high throughput assay development, assay validation tools, and thesis writng. You will be independently conducting laboratory work, analysing the data collected and organizing it into scientific presentations to your peers, and you will have the opportunity to actively and critically participate in the development of the project. 

Qualifications
Essential
A bachelor in biological sciences with a strong cell biology or biochemical focus.
Excellent organizational, communication and interpersonal skills, combined with the ability to work collaboratively across boundaries and problem solve in the absence of complete information.
Excellent communication skills in English (speaking, presenting and writing).

Desirable
Basic knowledge around handling mammalian cell culture
Experience working in a biochemical laboratory

 
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, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.

Application
Randstad Life Sciences is cooperating with AstraZeneca in this recruitment process. We only accept applications through Randstad's website.
 
Deadline for application: 2020-03-31, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.

 For more information: Kerstin Karlsson [email protected] or Eleonor Ehrman +4673-343 41 09.

About the company
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. Visa mindre

Arbetsbeskrivning
Är du en doer av rang som tycker om att ha en bredd i dina arbetsuppgifter? Du kanske är en ödmjuk men självutnämnd språkguru och samtidigt ett kundserviceproffs i grund och botten? Nu har vi på Randstad möjlighet att erbjuda ett längre konsultuppdrag som sälj-och marknadskoordinator hos Wellspect HealthCare. Om du identifierar dig med det ovannämnda vill jag gärna komma i kontakt med dig.


Uppdraget rent övergripande är att stödja de lokala nordiska marknaderna med marknadskommunikation och kundtjänststöd, både internt och externt. 
Som koordinator kommer du att leda den lokala anpassningen av digitalt och tryckt marknadsföringsmaterial. Detta inkluderar översättning av text och skapa / modifiera mindre innehåll. Du kommer också att hantera inkommande kundorder, leverantörsfakturor och klagomålshantering. I den här rollen kommer du att arbeta nära flera olika kontaktytor så som vårt Nordiska MarCom-team, Supplyavdelning,  promotionlager och den lokala försäljningsorganisationen. Sälj- och marknadskoordinatorn ansvarar också för att kunder och brukare får korrekt information och service genom alla kundservicekanaler samt andra administrativa uppgifter. Vi letar efter dig som talar och skriver flytande danska och engelska. 


Som konsult hos Randstad är du anställd hos oss och jobbar ute hos någon av våra kunder. Du har samma fördelar hos Randstad som hos andra arbetsgivare med kollektivavtal och förmåner som friskvårdsbidrag, företagshälsovård, försäkringar och rabatt på träningskort. Utöver det erbjuds du även en mängd karriärmöjligheter, får möta olika företagskulturer och erfarenhet från olika branscher vilket gör att du utvecklar din kompetens och får ett välfyllt CV. Tjänsten kan innebära många kontakter och då är det är viktigt med god samarbets- och kommunikationsförmåga. Som person ser vi att du är drivande och van att arbeta självständigt. Söker du en arbetsgivare som erbjuder varierande uppdrag och nya kontaktnät kommer du att trivas hos oss.



Ansvarsområden
- Projektleda lokal anpassning av marknadskommunikation


- Planering av lokala kundevenemang


- Hantera inkommande beställningar och omvandla dem till rätt produkter till rätt kunder i rätt tid.


- Ge kunder och slutanvändare support i världsklass.


- Delta aktivt i det nordiska marknads- och kundserviceteamet 



Arbetstider
Heltidsarbete, konsultuppdrag till en början med möjlighet till anställning för rätt person. Arbetstid: Mån-fre 08.00-17.00.



Kvalifikationer
- Några års marknadsföring och / eller kundtjänsterfarenhet.


- Du har starta kommunikativa egenskaper på danska och engelska


- Erfarenhet från marknadsföringsverktyg som InDesign och Hubspot.


- God kunskap inom programvara som Office- och ERP-system, såsom SalesForce och Movex.


- Erfarenhet från MedTech-branschen är starkt meriterande.


För oss är det viktigt att all kompetens på arbetsmarknaden tillvaratas. Vi välkomnar alla sökande och eftersträvar mångfald.



Erfarenhet
Erfarenhet av liknande roll eller motsvarande erfarenheter krävs.

Ansökan
Sista ansökningsdag 2020-02-25, urval och intervjuer kommer att ske löpande. Tjänsten kan komma att bli tillsatt innan sista ansökningsdag, ansök därför så snart som möjligt. 
För information: Maria Hellström, konsultchef [email protected].

Om företaget
Wellspect HealthCare, med huvudkontor i Mölndal i Sverige, är en ledande global leverantör av innovativa medicintekniska produkter och tjänster med fokus på hjälpa människor som lider av urinretention eller kronisk förstoppning. Varje dag arbetar mer än 1 100 engagerade medarbetare med att göra skillnad för de som behöver våra produkter och våra tjänster. Många av dem som vi hjälper har ryggmärgsskada, förstorad prostata, ryggmärgsbråck eller multipel skleros. Vi är en av världens ledande tillverkare av intermittenta urinkatetrar, med LoFric® som vårt mest kända varumärke. Som hjälp till de med kronisk eller svår förstoppning har vi utvecklat vad som sannolikt är världens mest avancerade irrigationssystem, Navina Systems™, vilket kombinerar en hög grad av användarvänlighet, klinisk effekt och kommunikation i ett verkligt smart system. Wellspect HealthCare är representerat i fler än 30 länder samt ingår i Dentsply Sirona, världens största tillverkare av professionella tandvårdsprodukter och teknologier med globalt huvudkontor i York, Pennsylvania i USA, samt internationellt huvudkontor i Salzburg i Österrike. Företagets aktier är listade på amerikanska NASDAQ under symbolen XRAY. Mer information finns på www.wellspect.com och www.denstplysirona.com.

Om randstad
Med över 600 000 anställda i omkring 40 länder är Randstad världsledande inom HR-tjänster och erbjuder bemannings-, konsult- och rekryteringslösningar inom alla kompetensområden. Vi erbjuder även interim management, executive search och omställningstjänster. Vi har ett stort nätverk av bolag och kandidater vilket innebär att vi förmedlar hundratals jobb inom olika branscher, från Kiruna i norr till Malmö i söder. Vår ambition är att vara den bästa arbetsgivaren på marknaden.


Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och organisationer att nå deras sanna potential. Vi kallar det Human Forward. Visa mindre

Job description
Are you a master’s student looking for thesis work with start autumn 2020? Are you interested in the pharmaceutical industry? AstraZeneca offers 30 and 60 credit thesis work within different areas of the company.  They are looking for motivated students passionate about science and willing to learn a broad range of new techniques.


About AstraZeneca
At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Our Gothenburg site is one of AstraZeneca's three strategic science centers. We thrive in a multinational environment working cross-functionally across the globe with AstraZeneca colleagues as well as academic and industry partners. 


Our way of life is to foster a working environment that nurtures collaboration, openness and innovation. Therefore, we have created space for meetings, socializing and relaxation, where spontaneous meetings can give birth to new innovations. The unexpected ideas or thoughts that can come from a chat over something as simple as a cup of coffee or a stroll on our "walk and talk" meeting trail. 

Responsibilities
AstraZeneca offers thesis projects in different areas. They include, but are not limited to, biomedical research, chemistry, data science, statistics.

This is a general advertisement for thesis work at AstraZeneca Gothenburg. Specific advertisements for the thesis projects will be published during March. Are you interested in doing your thesis work at AstraZeneca, we recommend that you apply here already today!

Qualifications
Currently enrolled as a student within a technical, scientific or other relevant field
A strong interest in pharmaceuticals or the pharmaceutical industry
Open and comprehensive scientific mindset
Written and oral communication skills in English
Ability to work collaboratively across boundaries and problem solve in the absence of complete information

For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
Randstad Life Sciences is cooperating with AstraZeneca in this recruitment process. 
We only handle applications sent through Randstad’s website.


All chosen candidates need to pass a background check and an alcohol and drug test before starting the project.


Deadline for application: 2020-03-29, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.

For more information: Contact Kerstin Karlsson, consultant manager, [email protected] or Eleonor Ehrman, consultant manager, +4673-343 41 09.

About the company
At AstraZeneca, we are guided in our work by a strong set of values, and we’re resetting expectations of what a bio-pharmaceutical company can be. By truly following the science, we pioneer new methods, new thinking and bring unexpected teams together. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that transform lives. 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. If you’re swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person. Visa mindre

Arbetsbeskrivning
Zinzino är en arbetsplats präglas av drivkraft och stort fokus på digitala marknadsplattformar och användarvänliga system. Vi närmar oss 100 anställda på huvudkontoret där vi arbetar nära våra kunder och återförsäljare som finns i 34 länder i Europa och Nordamerika. Vi håller till i superfina lokaler i Västra Frölunda, Göteborg. 

Ansvarsområden
På Zinzino har vi en miljö med högt i tak och kollegor med stort engagemang. Vi har som mål att förbättra och förändra befintliga system samt utveckla nya system inom hela vår infrastruktur. Detta gör att vi kan se fram emot många spännande utvecklingsprojekt för våra IT system. 


När vi nu är igång med att utveckla nästa generation av system och applikationer behöver vi utöka vårt team och framför allt vårt QA-team med en person som vill jobba med både kravinsamling och test. Du kommer att tillhöra vår R&D-avd på snart 18 pers varav 5 av oss jobbar mer eller mindre med test. Under det gångna året har vi ordentligt kommit igång med att kvalitetssäkra vårt arbete på ett strukturerat sätt men har fortfarande en del kvar att göra, framför allt när det gäller krav- och testautomatisering där vi vill utvecklas och bli bättre. Tillsammans med resten av teamet kommer du, som krav- och testspecialist vara högst delaktig i att vi tar ett helhetsansvar över kvalitetssäkring (QA) av våra system och applikationer.


I rollen som krav- och testspecialist planerar du och styr kravarbetet, samt arbetar med testplanering och tester. Du kommunicerar kravbilden till projektet (utveckling/test/arkitektur), samt säkerställer att teamet förstår kraven. Inom test innebär arbetet testplanering, du är med och skriver testfall utifrån kraven plus att du även är delaktig i att utföra tester. Vårt testarbete behöver bedrivas på olika områden såsom t ex integrationstester, prestandatester, test av mobila applikationer, användbarhetstester m m. Rollen hos oss innebär ofta att man arbetar i en miljö som kännetecknas av hög förändringstakt. Vi jobbar i en agil miljö och vi har stort fokus på kundnytta och slutresultat.

Kvalifikationer
Vi söker dig med erfarenhet av att ha arbetat med kravinsamling och test, du tycker om problemlösning och har lätt för att fånga upp detaljer och att sätta dig in i olika verksamheter. Du tycker om att hjälpa verksamheten att skapa samsyn och förståelse och du har insikten att både detaljer och flexibilitet är nödvändigt. 


Vi vill att du har god erfarenhet av kravinsamling och att bryta ner och tydliggöra kraven. Du har en god förmåga att omsätta verksamhetens behov till användbara krav. Du har erfarenhet av att leda workshops och genomföra intervjuer. Du har god erfarenhet inom test och testledning. Du har förståelse, kunskap och en nyfikenhet kring olika testverktyg och testmetoder och de kan användas effektivt i testarbetet. 


Vi tror att du har tidigare erfarenhet av agilt tillvägagångssätt. Vi vill att du behärskar både svenska och engelska i tal och skrift. Meriterande är certifieringar (ISTQB och IREB/REQB).


Som person är det viktigt att du är en lagspelare som brinner för att alla i teamet ska arbeta mot at uppfylla gemensamma mål. Du är flexibel och kan anpassa dig till nya situationer och arbetssätt. Du har en förmåga att driva din egen roll framåt, i e en stark personlig drivkraft, du är lyhörd, social och prestigelös. Vidare är du kommunikativ och har en pedagogisk ådra. 

Ansökan
I den här rekryteringen samarbetar vi med Randstad Technologies och Pia Tegnér. För information kontakta Pia Tegnér, rekryteringskonsult, [email protected] eller 0733-573607. Urval och intervjuer kommer att ske löpande. Tjänsten kan komma att bli tillsatt innan sista ansökningsdag, ansök därför så snart som möjligt.

Om företaget
Zinzino AB är ett globalt direktförsäljningsföretag som marknadsför och säljer testbaserade produkter inom kosttillskott, hudvård och livsstil. Zinzino äger det norska företaget BioActive Foods AS och forsknings-/produktionsenheten Faun Pharma AS. Zinzinos huvudkontor ligger i Göteborg och företaget har även kontor i Helsingfors, Riga, Oslo, Florida och Adelaide. Zinzino är ett aktiebolag noterat på Nasdaq First North. Visa mindre

Job description
At AstraZeneca, innovation is more than just research. As one of the world's leading pharmaceutical companies, we’re focused on providing medicines that make a real difference in patient care. AstraZeneca R&D Gothenburg is a great place to work where you can help us continue to lead the industry in research and development. It has an entrepreneurial and collaborative culture, where you’ll feel valued, energised and rewarded for your ideas and contributions. It is a place where talented people can immerse themselves in their work and make significant contributions towards scientific excellence.


You will join the Discovery Sciences organization, working within a vibrant scientific environment to support drug discovery. The Discovery Biology department of Discovery Sciences is responsible for the generation of novel reagents and assays to support projects in the IMED (Innovative Medicines and Early development) in all phases of the drug discovery pipeline, from target discovery all the way to clinical candidate. The IMED focuses on scientific advances in small molecules, oligonucleotides and other emerging technologies and drug discovery platforms across our different core areas.


There is an exciting opportunity for a talented and motivated individual to join the group in a lab-based role. The successful individual will be a key member of the team, contributing to and leading protein generation activities for a diverse range of projects across several disease areas and AstraZeneca sites globally. This is a temporary position, lasting for 6 months. 

Responsibilities
As a Research Scientist in the Biochemical Reagents team in Discovery Biology you will be responsible for producing and characterising recombinant proteins which represent disease targets for all small molecule drug discovery projects in the IMED, with a focus on Cardiovascular and Metabolic Disease (CVMD) and Respiratory, Inflammation and Autoimmunity (RIA) projects. Proteins are utilised for the development of biochemical assays for compound screening, structural/biophysical assays to characterise protein ligand interactions and to develop oligonucleotide drugs.

Main Duties and Responsibilities
To be a lab-based protein scientist, delivering recombinant proteins to support our projects
To provide expertise in the area of recombinant protein expression purification and characterisation.
To work in partnership with colleagues in Discovery Sciences and across therapy areas and sites to ensure the delivery of high-quality protein reagents to projects.
To deliver according to plans over agreed timelines such that the objectives of the project are met, including delivery of more than one agreed area of work in parallel where appropriate. 
To be an effective member of Drug Discovery Project Teams, contributing novel ideas and using judgment and knowledge where appropriate to influence the work of the project. 
To maintain an awareness of current developments in the literature and contribute to the continuous improvement process by identifying opportunities in the workplace where improvements can be made. 


Qualifications
Essential Requirements
BSc/MSc degree in biochemistry with significant relevant experience, preferably in the pharmaceutical or biotechnology industry. 
Expertise in the area of Protein Science through a demonstrable knowledge of construct design, molecular biology, protein expression, purification, characterisation and structure function.
 A practical understanding of a wide range of methods and technologies as applied to the expression, purification and characterisation of recombinant proteins. For example, bacterial expression, liquid chromatography.
Good problem-solving skills, good scientific judgement and communication skills.
Excellent team working and networking skills with experience of interacting effectively across teams



Desirable Requirements
PhD in biochemistry
Experience of parallel purification
Experience of purification of proteins from native sources.

For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-02-02, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


For more information: Kerstin Karlsson [email protected] or Eleonor Ehrman +46733434109. 

About the company
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.


Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! 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. Individuals are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity

Responsibilities
As a Statistical Programmer you would join a team of statistical programmers in early CVRM/RIA Biometrics and act as the main programmer of a Phase I-II trials.

Qualifications
Required Background
Minimum educational level is a BSc degree in a relevant subject such as biostatistics, mathematics, computer science or life science.
Minimum of 5 years SAS programming experience in the Pharma sector (CRO/industry).
Expertise in CDISC standards (SDTMs, ADaM), TLFs production and CRT packages.
Good collaboration, communication, leadership and influencing skills
Good written and spoken English

 
Additional background
Experience in CVRM/RIA disease areas is desirable

 
Personal Qualities 
Candidates should possess good social skills, be strong team players and be able to work effectively in a global organization where teams often are geographically dispersed. You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude.
 
It is essential to have good organizational and communication skills and you should be able to analyze and summarize your results and be comfortable in presenting them. Successful candidates will have the ability to communicate subject matter expertise to other experts, as well as an interest in the application of programming in pharmaceutical development. 

For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-02-03, selection and interviews will be ongoing. The position may be filled before the last day.

For more information:  Eleonor Ehrman, consultant manager,  +4673-343 41 09 or Kerstin Karlsson, consultant manager, [email protected].

About the company
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.

Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! 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


At AstraZeneca, science is at the core of everything we do. Our purpose is to push the boundaries of science to deliver life-changing medicines. Would you like to be a part of helping us achieve this ambition?


Explore the possibility of joining us as Associate Information Scientist (AIS)within one of our key scientific focus areas Respiratory, Inflammation and Autoimmune (RIA). Supporting the late stage drug project teams, you will be a key person for innovative use of information and data to help shape our trials, decision making and portfolio. 

The Arena
You will play a leading role in supporting global clinical teams in finding and structuring clinical information for late stage drug development decisions. The position sits within our Information Practice unit who drives optimal use and value of clinical information and scientific knowledge retention for better informed decision-making in clinical development. 


Late-stage Development RIA Biometrics consists of statistical, programming and information experts for drug development in phase II and beyond. You will be part of a truly global team alongside some of the most respected specialists in the industry.

Responsibilities
Support RIA TA Memory 


Tasks include: 
find, download, and make available key information for selected disease populations and competitors
adjust and work with current SPOL site from a technical perspective
on a regular basis go through and ensure information in library are current
support and expand current information user and supplier network to ensure we get access to available information 

 
By information we mean publications, supplemental information, public CSRs and other documents, HA documentation, guidance documents for this disease and any other information that might help the clinical project teams

Qualifications
Minimum requirements
Bachelors or advanced degree in a Life Science
Experience in clinical information or science information setting in the application of information and knowledge management (settings could include, but are not limited to clinical drug development, medical writing, medical affairs, clinical operations, competitive intelligence, regulatory intelligence)
Good organizational skills and the ability to multitask; can set priorities and follow a timeline
Ideally a self-starter, who can work independently
Good written and verbal communication skills



Preferred experience and key factors
Good understanding of project management techniques and methods 
Knowledge of the pharmaceutical clinical drug development process (with a preference for late-stage drug development in Respiratory, Inflammation, Autoimmunity) 


For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-01-22, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


For more information: Birgitta Nyström, consultant manager, birgitta.nystrom.se or Kerstin Karlsson, consultant manager, [email protected].


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 the company
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 Visa mindre

Job description
Do you have experience within analytical and biophysical characterization of biomolecules and enjoy working in the lab? Are you interested in working with a broad array of molecules and analytical techniques in the pharmaceutical product development area? We are looking for you that are an analytical chemist with experience of biomolecule characterization and working according to Good Manufacturing Practice (GMP).

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
 
AstraZeneca is now seeking two Analytical Scientists to join their New Modality CMC Analytics team within the Advanced Drug Delivery (ADD) function that is part of Pharmaceutical Sciences at AstraZeneca in Gothenburg, Sweden.
 
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. Our portfolio of projects spans traditional small molecules, peptides, oligonucleotides to RNA based therapeutics across AstraZeneca’s therapy areas. Advanced Drug Delivery (ADD) resides within Pharmaceutical Sciences with a mission to provide novel products to AstraZeneca’s clinical pipeline.

Responsibilities
As a Scientist working in the clinical development phase within ADD you will support drug projects from an analytical perspective, from candidate drug nomination over Phase 2 clinical trials. You will focus on characterization of various molecules, primarily oligonucleotides, using several different analytical techniques. The role covers development and validation of analytical methods, stability studies, release analysis, and other type of analytical support to drug projects. Part of the work is performed according to GMP. You will work as a member of cross-functional pharmaceutical project teams and in close collaboration with other analysts, formulators, chemists and biologists at AstraZeneca in Sweden, UK and US.
 
Preferably, you should be experienced in analytical and biophysical characterization of biomolecules as well as working in pharmaceutical development, including working according to GMP. You should possess an enthusiasm for laboratory-based work, be flexible and have a problem-solving mind-set. 


 
Main Duties and Responsibilities
Give analytical support to drug development projects, such as stability studies, release analysis and other supportive characterization experiments, using techniques like UV spectrophotometry, LC-UV/MS and liquid particle counting.
Development and validation of analytical methods.
Generate, evaluate and report data clearly and reliably. 
Prepare documentation and formal reports in accordance with current standard procedures and where appropriate, according to GMP standard. 
Give analytical support to scientific initiatives on new technologies/processes together with specialists and/or technology networks. 
Working as a member of cross-functional drug development project teams.


Qualifications
Essential Requirements
MSc degree in a relevant scientific discipline (e.g., Analytical Chemistry, Biochemistry or Biotechnology).
In-depth knowledge of analytical methodologies such as chromatography, mass spectrometry and biophysical characterization techniques.
Thorough understanding of principles and applications of Good Manufacturing and Laboratory Practices (GMP/GLP).
Ability to communicate in English both orally and in writing.

 
Desirable Requirements
3+ years of industrial experience of analytical work with biomolecules in clinical drug development phase.
Qualified to execute analytical work according to GMP.
An interest in exploratory analytical work related to complex molecules and new technologies.


For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-01-16, selection and interviews will be ongoing. The position may be filled before the last day.
For more information:  Eleonor Ehrman, consultant manager,  +4673-343 41 09 or Kerstin Karlsson, consultant manager, [email protected].

About the company
 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.

Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Job description
Do you have experience within formulation and biophysical characterization of biomolecules and enjoy working in the lab? Are you interested in working with a broad array of molecules and formulations in the pharmaceutical product development area? We are looking for you that are a formulation chemist with experience of biomolecule characterization.

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.

AstraZeneca is now seeking two Formulation Scientists to join their New Modality Clinical Formulation and Bioscience team within the Advanced Drug Delivery (ADD) function that is part of Pharmaceutical Sciences at AstraZeneca in Gothenburg, Sweden.
 
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. Our portfolio of projects spans traditional small molecules, peptides, oligonucleotides to RNA based therapeutics across AstraZeneca’s therapy areas. Advanced Drug Delivery (ADD) resides within Pharmaceutical Sciences with a mission to provide novel products to AstraZeneca’s clinical pipeline.

Responsibilities
As a Scientist working in the clinical development phase within ADD you will support drug projects from a formulation perspective, from candidate drug nomination over Phase 2 clinical trials. You will focus on various oligonucleotides projects, delivering formulations to toxicology studies and supporting formulation development. You will work as a member of cross-functional pharmaceutical project teams and in close collaboration with other analysts, formulators, chemists and biologists at AstraZeneca in Sweden, UK and US.
 
Preferably, you should be experienced in formulation chemistry as well as working in pharmaceutical development. You should possess an enthusiasm for laboratory-based work, be flexible and have a problem-solving mind-set. 


 
Main Duties and Responsibilities
Support drug development projects, such as toxicology and stability studies.
Perform essential characterization of the formulations e.g. pH, density, viscosity and osmolality.
Development and validation of biophysical characterization methods.
Generate, evaluate and report data clearly and reliably. 
Prepare documentation and formal reports in accordance with current standard procedures. 
Give formulation support to scientific initiatives on new technologies/processes together with specialists and/or technology networks. 
Work as a member of cross-functional drug development project teams.


Qualifications
Essential Requirements
MSc degree in a relevant scientific discipline relevant to formulation science (e.g., chemistry, pharmaceutical technology, surface & colloid chemistry or equivalent qualifications).
Basic knowledge of analytical methodologies such spectrometry and biophysical characterization techniques.
Understanding of principles and applications of Good Laboratory Practices (GMP/GLP).
Ability to communicate in English both orally and in writing.

 
Desirable Requirements
3+ years of industrial experience of formulation work of biomolecules in clinical drug development phase.
An interest in exploratory formulation work related to complex molecules and new technologies.


For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-01-16, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


For more information:  Eleonor Ehrman, consultant manager,  +4673-343 41 09 or Kerstin Karlsson, consultant manager, [email protected].

About the company
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.

Randstad Life Sciences is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Job description
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But they're more than one of the world's leading pharmaceutical companies. At AstraZeneca, they are proud to have a phenomenal workplace culture that encourages innovation and collaboration. The employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. 


For a consultant position, we at Randstad Life Sciences are looking for a motivated individual to take on take on the role as Drug Metabolism and Pharmacokinetics (DMPK) Project Leader (DPL) for 12 months. Alternatively, it can be an opportunity for a highly talented individual with less specific experience to assist an experienced DPL whilst training for the role. The DPL role is a strategic and scientific role where you will be a member of the project team and work cross functionally and closely with the toxicologist, bioscientist and clinical pharmacologist in various stages of drug development beginning with candidate drug nomination. You will lead and coordinate all non-clinical DMPK work including assessment of drug-drug interaction potential, pharmacokinetic/pharmacodynamic data analysis, estimation of safety margins, biotransformation (including human) and delivery of non-clinical pharmacokinetics regulatory summary documents for compound progression. 


You are expected to have understanding of DMPK and drug development to be able to provide advice and interpretation of complex data. 

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
Lead DMPK- activities related to evaluating, mitigating and highlighting any development risks related to pharmacokinetic and pharmacodynamic drug properties including absorption, distribution, clearance, elimination and biotransformation. 
Deliver DMPK data and interpretation to projects within agreed timelines and to the right quality 
Accountable together with Bioscience and Toxicology functional leads to plan and conduct non-clinical studies of drug candidates to support first in human dosing. 
Apply an understanding of DMPK and regulatory requirements to address DMPK related risks and take advantage opportunities for simplification. 
Responsible for leading, coordinating and engaging with Early RIA DMPK colleagues and contract research organizations in project related activities 
Prepare clear presentations related to the above for internal governance bodies.


Qualifications
Formal training or proven experience of working with pharmacokinetics and drug metabolism. 
Hands-on knowledge of pharmacokinetic data analysis. 
PhD or equivalent experience in a relevant discipline (Pharmacokinetics, toxicology, , Pharmaceutics). 
Understanding of regulatory requirements related to DMPK and ADME.
Experience from drug discovery or development cross-functional project work is desirable. 
Ability to engage and collaborate across boundaries with a problem solving attitude and focus on delivery.

For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-01-14, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


For more information, please contact Eleonor Ehrman, Consultant Manager [email protected].

About the company
With more than 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry and offers staffing, consulting and recruitment solutions in all areas of expertise. We also offer interim management, executive search and outplacement services. We have a large network of clients and candidates, which means that we convey hundreds of jobs within different industries all over Sweden. Our ambition is to be the best employer in the market. 

By combining our passion for people with the power of today’s technology, we help people and organizations to reach their true potential. We call it Human Forward. Visa mindre

Job description
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But they're more than one of the world's leading pharmaceutical companies. At AstraZeneca, they are proud to have a phenomenal workplace culture that encourages innovation and collaboration. There, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

For a consultant position, Randstad Life Sciences is now looking for a motivated individual to take on the role as Drug Metabolism and Pharmacokinetic (DMPK) Design Leader (DDL) for 12 months. Alternatively, it is an opportunity for a highly talented indivudal with less specific experience to assist an experienced DDL whilst training for the role. The DDL role is a strategic and scientific role where you will work closely with Medicinal Chemistry, Bioscience and representatives from other functions in drug discovery. You will influence chemical drug design by optimizing the ADMET (absorption, distribution, metabolism, excretion, toxicity) for compounds within projects. In addition to oral drugs, the task is also to optimize inhalation properties for projects aiming for this route of administration.

The successful applicant will contribute to RIA drug design teams by providing DMPK expertise and input to the design of new compounds. This includes analysis of ADMET and efficacy data and to develop a strategy for how to improve these and subsequently influence project progression.

You are expected to have understanding of DMPK and chemistry to be able to provide advice and interpretation of complex drug discovery data.

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
Lead DMPK-related activities and the optimisation of compounds by balancing the properties associated with absorption, distribution, clearance, elimination and lung targeting to ensure that DMPK challenges are thoroughly assessed and resolved
Deliver DMPK input and data to projects within agreed timelines and to the right quality
Accountable together with Medicinal Chemistry, Bioscience and Safety, for compound design and effective cross-discipline optimization and Design-Make-Test-Analysis (DMTA) cycles in drug discovery
Apply an understanding of DMPK and physicochemical properties to support/influence compound design, project progression and project strategy
Responsible for leading, coordinating and engaging with RIA DMPK colleagues in project related activities
Prepare clear presentations related to the above for internal governance bodies


Qualifications
Formal training or proven experience of working with pharmacokinetics and drug metabolism.
PhD or equivalent experience in a relevant discipline (Medicinal, Organic or Physical Chemistry or bio-pharmaceutics/pharmacokinetics)
Understanding of correlations between physicochemical characteristics and their influence on DMPK properties and subsequent design of new compounds.
Experience from drug discovery cross-functional work and compound/project progression is desirable
Ability to engage and collaborate across boundaries with a problem solving attitude and focus on delivery

For us at Randstad, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2020-01-14, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


For more information: please contact Eleonor Ehrman, Consultant Manager [email protected] .

About the company
With more than 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry and offers staffing, consulting and recruitment solutions in all areas of expertise. We also offer interim management, executive search and outplacement services. We have a large network of clients and candidates, which means that we convey hundreds of jobs within different industries all over Sweden. Our ambition is to be the best employer in the market. 

By combining our passion for people with the power of today’s technology, we help people and organizations to reach their true potential. We call it Human Forward. Visa mindre

Arbetsbeskrivning
Lockas du av en internationell miljö med många kontaktytor där du får leverera högsta service till kund? Är du ansvarstagande och flexibel som person och trivs med att jobba i en laborativ miljö? Avantor Services söker nu en serviceinriktad laboratorietekniker till sin verksamhet på AstraZeneca!
 
Tjänsten som laboratorietekniker är placerad in-house på AstraZeneca och innebär ett ansvar för labb support till AstraZenecas laborativa verksamhet. I rollen utför du supporttjänster vilka fungerar som ett direkt och indirekt stöd till forskare inom olika funktioner och avdelningar på AstraZeneca. Du kommer att arbeta i ett team om 12 Laboratorietekniker och tillsammans delar ni intresset av att serva era kunder på labb.   

Ansvarsområden
Arbetsuppgifter:
·         Hantering av labbdisk
·         Tömning och påfyllning av labbrockar/kläder
·         Underhåll av olika instrument (både i och utanför GMP miljö)
·         Autoklavering av olika material 
·         Tillverkning av olika typer av media och buffertar (både i och utanför GMP miljö)
·         Enklare kontroll av pipetter
·         Arkivering av instrument- och utrustningsdokument
·         Säkra upp serviceleveransen genom att utbilda kollegor på ditt arbetsområde och vara beredd att lära dig nya områden


I rollen ingår även att arbeta generellt med förbättring och optimering av befintliga processer, samt aktivt jobba med att utvärdera och implementera nya arbetsuppgifter efter behov från AstraZenecas forskningsverksamhet. Det är en mångfacetterad roll som ska utföras på ett säkert, regelmässigt och arbetsmiljömässigt korrekt sätt.

Tjänsten är en tillsvidareanställning på heltid hos Avantor Services. 
 

Kvalifikationer
Vi söker dig som har en relevant teknisk eller naturvetenskaplig utbildning på lägst gymnasienivå. Du har erfarenhet av laboratoriearbete och förståelse för laborativ verksamhet. Du har tidigare arbetat med riktlinjer och rutiner för hälsa, miljö och säkerhet. Du är dessutom kunnig i datainsamling, analys och rapportering med hjälp av olika IT system och t.ex. Microsoft Excel. Goda kunskaper i svenska och engelska i både tal och skrift är en förutsättning för att lyckas i tjänsten. Har du kunskap inom GMP ses det som ett stort plus. Då en stor del av arbetet innefattar kontakt med kunder är erfarenhet av kundrelationer meriterande.
 
 Då vi arbetar tätt tillsammans, kommer dina personliga egenskaper att värdesättas högt. Du är bra på att kommunicera och du värderar noggrannhet, säkerhet och service högt. Du är en utpräglad team-människa och har lätt för att samarbeta, samtidigt som du har en god förmåga att driva ditt arbete framåt. Som person kan du enkelt prioritera mellan dina arbetsuppgifter och du är flexibel och strukturerad och kan hantera flera ansvarsområden och uppgifter regelbundet. Då tjänsten innebär olika typer av arbete på lab är det viktigt att du trivs med att vara aktiv samt klarar vissa tunga lyft. Du tar en aktiv roll i teamet och delar gärna med dig och bidrar till en positiv stämning.
 
 Om du tror att du skulle trivas hos oss, är du välkommen med din ansökan!
 



Ansökan
Ansök med CV och ett motiverat brev senast den 8 januari 2020. Vi tillämpar löpande urval, så ansök gärna så snart som möjligt. I den här rekryteringen samarbetar Avantor Services med Randstad LifeSciences & Engineering och rekryteringskonsult Nadja Bergman 072-988 98 28. 
 



Om företaget
”VWR International, part of Avantor” är den ledande leverantören av laboratorieutrustning till laboratorier. Produktsortiment omfattar kemikalier, glas- och plastutensilier, apparater, instrument och laboratorieinredningar. VWR säljer och marknadsför laboratorieprodukter från världsledande leverantörer runt om i världen.


Affärsområdet Avantor Services erbjuder högkvalitativ Lab Service integrerat hos kunder inom främst läkemedelsindustri med målet att förbättra produktivitet och vetenskaplig innovation hela vägen från laboratoriet till produktutveckling. Genom att utnyttja Avantor Services flexibla och anpassningsbara tjänster kan våra kunder fokusera på deras kärnverksamhet och nå sina mål på ett effektivare och snabbare sätt. Visa mindre

Job description
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world’s leading pharmaceutical companies?

The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca’s pharmaceutical development organizations deal with all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase. You will also have the possibility to contribute with expert advice to the pharmaceutical development functions and to the delivery of our pipeline of exciting new medicines.

Responsibilities
The role
In your role you will have a lot of interactions with internal and external stakeholders as well as with vendors and suppliers.
Provide QA advice into internal/external manufacturing activities of Drug Product and patient medication
Perform QA release of internally/externally manufactured and packed Drug Product as part of the Supply Chain to clinical trials
Support the pharmaceutical development functions with investigations of deviations, complaints, changes and other quality and compliance decisions in the development projects
Provide QA support to pharmaceutical development project with daninterpretation of GMP regulations 
Provide appropriate QA input to business improvement projects
Collaboration with AstraZeneca QA colleagues globally


The role may also include
Responsible for QA advice and approval of documentation related to manufacturing equipment and facilities to ensure compliance, including maintenance, calibration, validation and change control
Interpret, trend and report compliance data, to measure and improve quality standards within the pharmaceutical development functions.
Develop QA Agreements with suppliers or contractors delivering services or products to the pharmaceutical development Supply Chain. 


Qualifications
Minimum requirements – Education and Experience
MSc in pharmacy or engineering (specializing in Pharmaceuticals) with at least 3 years’ experience of working within a pharmaceutical GMP environment
Broad understanding of Quality Systems and GMP
Comprehensive understanding of the pharmaceutical/drug development process
Good communicator with experience of interacting effectively across interfaces
Fluent in written and spoken English


Preferred requirements
Experience preferably within a pharmaceutical manufacturing organization
Good team working and networking skills
Capable of making effective decisions
Demonstrate a high degree of personal credibility


For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.



Application
2019-11-12, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


For more information: Birgitta Nyström, consultant manager, [email protected] or Kerstin Karlsson, consultant manager [email protected].



About the company
Randstad Life Sciences specializes in the field of science and is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Arbetsbeskrivning
Är du nyutexaminerad eller senior inom IT/Programmering och har ett brinnande intresse för utveckling och teknik? Har du goda programmeringskunskaper i C#? Vill du få chansen att bli en del av ett härligt företag med stark laganda och gemenskap där man samtidigt värdesätter individens utveckling? Då har du möjligheten nu. Sök jobbet redan idag.  

Atea Global Services (AGS) är ett dotterbolag till Atea, Nordens ledande IT-infrastrukturföretag med mer än 7 000 anställda. De fungerar som Ateas globala operations center (GOC) och levererar tjänster i världsklass med fokus på den digitala arbetsplatsen så som Services Desk, Applikations paketering och tjänster inom Azure. AGS utvecklar även mjukvaruprodukter med fokus på den digitala arbetsplatsen och ligger i framkant för självbekännande support. 

På företaget råder balans som ger utrymme för kreativitet, utveckling och chans att påverka. Som anställd blir man en del av ett erfaret team på ett bolag med en stark grund att stå på. Samtidigt råder dock en mer utpräglad entreprenörskänsla på företaget där man driver sin egen verksamhet och har sin egen kultur. AGS utvecklar och jobbar med aktuella och spännande lösningar som ligger i framkant. Du kommer bli en del av ett glatt team bestående av 14 medarbetare. Inledningsvis kommer du att ha en mentor som introducerar och stöttar dig i ditt arbete.

Rollen som Systemutvecklare är ett uppdrag där du inledningsvis kommer att få anställning hos Randstad Technologies men med ambition att på sikt gå över i anställning hos kund. För rätt person kan det bli aktuellt med direktrekrytering. 

Ansvarsområden
I rollen som systemutvecklare blir din primära uppgift att utveckla i C# och konfigurera mjukvarubaserade produkter kopplat till den digitala arbetsplatsen. Scripting i PowerShell förekommer också. Du kan komma att utveckla  allt ifrån självbetjäningsportaler till projektplaneringsverktyg mot kundernas önskemål. Arbetet är förlagt mestadels in-house men besök hos kund förekommer. 

Arbetstider
Heltid

Kvalifikationer
• Högskoleexamen / YH-utbildning inom Data/IT
• Goda kunskaper i .Net och C#
• kunskaper
• Du kommunicerar obehindrat på engelska och svenska

Meriterande kompetenser
• Angular
• Active Directory 
• PowerShell
• Hobbyprojekt
• HTML
• CSS3
• Javascript
• Webforms
• Azure cloud services



Erfarenhet
Eftergymnasial utbildning inom IT/Programmering och goda kunskaper i C# och .

Ansökan
2019-12-31 urval och intervjuer kommer att ske löpande. Tjänsten kan komma att bli tillsatt innan sista ansökningsdag, ansök därför så snart som möjligt. Då det är sommartider kan det dröja något längre innan man får återkoppling

för information: Tova Dahlgren [email protected]



Om företaget
Randstad Technologies är specialister inom IT. Som konsult hos oss får du konkurrenskraftig lön, förmåner och kollektivavtalade villkor. Din konsultchef, som alltid finns nära till hands, ser till att du får varierande och utvecklande uppdrag på olika företag, inom olika branscher. Hos Randstad Technologies står din personliga utveckling i fokus, och du erbjuds ett stort nätverk och många sociala aktiviteter. 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. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
 
The arena
Pharmaceutical Sciences is accountable for the design and development of synthetic routes, preclinical and phase I/II formulations, analytical methods and CMC project leadership needed to support early clinical trials, encompassing both small molecules and new modalities such as microRNA, messenger RNA and antisense oligonucleotides, across the whole range of AstraZeneca’s therapeutic areas.
 
Drug Product Manufacture (DPM) in Gothenburg manufactures investigational products (oral solution/suspension, parenteral solutions, capsules, tablets and inhalers) to AstraZeneca’s clinical studies mainly in phase I/II around the globe and is a vital part of the Pharmaceutical Sciences organisation. 

Responsibilities
The role
At DPM, in the GMP (Good Manufacturing Practice) arena, you will make an important contribution in delivering clinical results in the development of new medicines. This role revolves around the manufacturing of drug product where all activities below will have a significant impact on the speed, quality and cost of the AZ development portfolio. We expect the successful candidate to:


Assume responsibilities toward timely and cost-effective manufacture of various drug products in line with the plans agreed within DPM, with focus on practical hands-on work in our pilot plant GMP facilities. 
Display strong competence as a process scientist with credibility and ability to give assured technical direction for product establishment and scale-up. 
Set up Master Manufacturing Records and Batch Records and perform transactions in Warehouse Management System through the Supply Chain IT-systems.
Assess records and report manufacturing and validation data accurately according to GMP. 
Ensure that SHE (Safety Health and Environment) and GMP standards are upheld and ensure AZ Policies and Standards are understood and followed.
Recommend ways to improve flexibility and productivity, including new ways of working, resulting in shorter lead times. 


Qualifications
Experience/requirements
We are looking for a scientist with excellent communication, planning and collaboration skills with the ability to operate independently to drive delivery of projects.  


MSc in pharmacy or engineering (specialising in Pharmaceuticals). Experience from pharmaceutical development or working in a manufacturing or supply chain organisation is required. You will have knowledge of cGMP and display excellent documentation skills, both in English and Swedish. You will also have a good understanding of, and interest in, manufacturing equipment. 
 
When publishing an ad for this assignment you may write that it is a consulting assignment at AstraZeneca as long as it is explicitly clear that it is a consulting assignment. All chosen candidates need to go through a background check and do an alcohol- and drug test.
 
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.

Application
2019-12-05, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.
 
For more information: Eleonor Ehrman, Consultant manager +4673-343 41 09 or Kerstin Karlsson, Consultant manager +4673-084 86 95.

About the company
Randstad Life Sciences specializes in the field of science and is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Arbetsbeskrivning
Zinzino är en arbetsplats präglas av drivkraft och stort fokus på digitala marknadsplattformar och användarvänliga system. Vi närmar oss 100 anställda på huvudkontoret där vi arbetar nära våra kunder och återförsäljare som finns i 34 länder i Europa och Nordamerika. Vi håller till i superfina lokaler i Västra Frölunda, Göteborg. 

På Zinzino har vi en miljö med högt i tak och kollegor med stort engagemang. Vi har som mål att förbättra och förändra befintliga system samt utveckla nya system inom hela vår infrastruktur. Detta gör att vi kan se fram emot många spännande utvecklingsprojekt för våra IT system. 

När vi nu är igång med att utveckla nästa generation av system och applikationer behöver vi utöka vårt team med ytterligare en mjukvarutestare. Du kommer att tillhöra vår R&D-avd på snart 17 pers varav 4 av oss jobbar mer eller mindre med test. 

Ansvarsområden
Vi blir bättre och bättre på att kvalitetssäkra vårt arbete men har fortfarande en del kvar att göra, framför allt när det gäller testautomatisering där vi vill utvecklas och bli bättre. Som mjukvarutestare hos oss kommer du att genomföra manuella tester men även bidra till att vi kan genomföra, automatisera och utveckla nya testmetoder. Vi önskar att du är med och driver och utvecklar arbetet med testautomatisering framåt. Tillsammans med övriga testteamet kommer du att utforma testplaner och lösningar för att implementera och testa både ny och befintlig funktionalitet. Vi tror att du kommer att vara viktig för oss när det gäller att förbättra och utveckla metoder och processer. Vi jobbar agilt och vi har stort fokus på kundnytta och slutresultatet.

Kvalifikationer
Vi vill att du har några års erfarenhet av kvalitetssäkring av mjukvara med hjälp av både manuella och automatiserade tester. Tillsammans med teamet är du med och planerar testarbetet, du är med och prioriterar, resurssäkrar, följer upp och förbättrar testprocessen. Vi tror att du har tidigare erfarenhet av agilt tillvägagångssätt. Vi tror också att du behärskar både svenska och engelska i tal och skrift.


Vi vill gärna att du har erfarenhet och kunskap inom: 
Automatiserade tester (främst GUI)
Last- och prestandatester
Skriptning
Uppsättning och orkestrering av testmiljöer
Framtagning av testdata

Meriterande är:
Certifieringar (ISTQB och IREB) är meriterande
Erfarenhet av flera verktyg inom testautomatisering
Kunskap i något programmeringsspråk kopplat till testautomatisering

Du är en teamplayer och vi ser gärna att du är en driven, engagerad och social person som vill vara med och aktivt påverka. Du tycker om att dela med dig av din kunskap till andra och ta feedback från dina kollegor. Vidare har du ett genuint intresse för att lära dig nya saker. Du är kvalitetsmedveten, strukturerad och ambitiös.

Ansökan
I den här rekryteringen samarbetar vi med Randstad Technologies och Pia Tegnér. För information kontakta Pia Tegnér, rekryteringskonsult, [email protected] eller 0733-573607. Urval och intervjuer kommer att ske löpande. Tjänsten kan komma att bli tillsatt innan sista ansökningsdag, ansök därför så snart som möjligt.

Om företaget
Zinzino AB är ett globalt direktförsäljningsföretag som marknadsför och säljer testbaserade produkter inom kosttillskott, hudvård och livsstil. Zinzino äger det norska företaget BioActive Foods AS och forsknings-/produktionsenheten Faun Pharma AS. Zinzinos huvudkontor ligger i Göteborg och företaget har även kontor i Helsingfors, Riga, Oslo, Florida och Adelaide. Zinzino är ett aktiebolag noterat på Nasdaq First North. 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

Job Description
Do you have experience within analytical and biophysical characterization of biomolecules and enjoy working in the lab? Are you interested in working with a broad array of molecules and analytical techniques in the pharmaceutical product development area? We are looking for you that are an analytical chemist with experience of biomolecule characterization and working according to Good Manufacturing Practice (GMP).

AstraZeneca is now seeking two Analytical Scientists to join their New Modality CMC Analytics team within the Advanced Drug Delivery (ADD) function that is part of Pharmaceutical Sciences at AstraZeneca in Gothenburg, Sweden.

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. Our portfolio of projects spans traditional small molecules, peptides, oligonucleotides to RNA based therapeutics across AstraZeneca’s therapy areas. Advanced Drug Delivery (ADD) resides within Pharmaceutical Sciences with a mission to provide novel products to AstraZeneca’s clinical pipeline.

As a Scientist working in the clinical development phase within ADD you will support drug projects from an analytical perspective, from candidate drug nomination over Phase 2 clinical trials. You will focus on characterization of various molecules, primarily oligonucleotides, using several different analytical techniques. The role covers development and validation of analytical methods, stability studies, release analysis, and other type of analytical support to drug projects. Part of the work is performed according to GMP.You will work as a member of cross-functional pharmaceutical project teams and in close collaboration with other analysts, formulators, chemists and biologists at AstraZeneca in Sweden, UK and US.Preferably, you should be experienced in analytical and biophysical characterization of biomolecules as well as working in pharmaceutical development, including working according to GMP. You should possess an enthusiasm for laboratory-based work, be flexible and have a problem-solving mind-set. 

Responsibilities
Give analytical support to drug development projects, such as stability studies, release analysis and other supportive characterization experiments, using techniques like UV spectrophotometry, LC-UV/MS and liquid particle counting.
Development and validation of analytical methods.
Generate, evaluate and report data clearly and reliably. 
Prepare documentation and formal reports in accordance with current standard procedures and where appropriate, according to GMP standard.
Give analytical support to scientific initiatives on new technologies/processes together with specialists and/or technology networks. 
Working as a member of cross-functional drug development project teams.




Qualifications
Essential Requirements
MSc degree in a relevant scientific discipline (e.g., Analytical Chemistry, Biochemistry or Biotechnology).
In-depth knowledge of analytical methodologies such as chromatography, mass spectrometry and biophysical characterization techniques.
Thorough understanding of principles and applications of Good Manufacturing and Laboratory Practices (GMP/GLP).
Ability to communicate in English both orally and in writing.



Desirable Requirements
3+ years of industrial experience of analytical work with biomolecules in clinical drug development phase.
Qualified to execute analytical work according to GMP.
An interest in exploratory analytical work related to complex molecules and new Technologies


For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
2019-11-17, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


For more information: Eleonor Ehrman, Consultant manager, +4673-343 41 09 or Kerstin Karlsson, Consultant manager, +4673-084 86 95.

About the company
Randstad Life Sciences specializes in the field of science and is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Arbetsbeskrivning
Vill du bli del av ett framgångsrikt företag som är världens ledande tillverkare av verktygsstål? Har du ett stort teknikintresse och drivs av att skapa goda relationer med dina kunder? Då kan rollen som Teknisk Innesäljare på voestalpine (Uddeholm) vara rätt utmaning  för dig!    

Som innesäljare på voestalpine i Mölndal arbetar du självständigt i ett team bestående av sex stycken innesäljare samt utesäljare och regionchefer. I rollen som teknisk innesäljare kommer du att ansvara för den dagliga kontakten med våra kunder och supportera dem via telefon och mejl. Relationen med kunden har ett stort värde vilket gör att kundvård och samarbete med kunder och det övriga teamet är mycket viktig. I rollen som teknisk innesäljare får du kontinuerligt teknisk utbildning på våra produkter. Vi vill ligga i framkant för att kunna utveckla våra kunder och säkerställa försäljning av de produkter som voestalpine erbjuder. 

Ansvarsområden
- Ansvara för rådgivning till kunder gällande materialval
- Stötta kunder med teknisk rådgivning
- Aktivt bearbeta och sälja till våra kunder över telefon
- Ordermottagning och registrering i affärssystem
- Ansvara för offertgivning och affärsavslut
- Ansvara för inköp från leverantörer
- Ansvara för att egna kundorder blir fakturerade

Arbetstider
Heltid, Tillsvidare

Kvalifikationer
Du som söker har gärna en teknisk utbildning på lägst gymnasienivå. Flytande norska och engelska i tal och skrift är ett krav. Vi ser gärna att du tidigare har arbetat med försäljning och är van vid att hantera och stötta kunder över telefon och mejl. Erfarenhet från tillverkande industri ses som en stor fördel. Att du har ett tekniskt intresse ser vi som självklart. 

För att vara framgångsrik i rollen är det viktigt att du är noggrann, ansvarsfull och en skicklig administratör. Som person är du serviceinriktad och trivs med att dagligen ta kontakt med kunder på eget initiativ. Du är självgående, samtidigt som du har en god samarbetsförmåga och ditt engagemang för kunden och affären gör att du ser möjligheter i varje utmaning. 

Ansökan
I den här rekryteringen samarbetar voestalpine med Randstad Engineering. Har du frågor om tjänsten är du välkommen att kontakta rekryteringskonsult Malin Tossavainen, [email protected]

Sista ansökningsdag: 2019-12-15

Om företaget
Sedan 2007 ingår Uddeholm i den internationellt börsnoterade stålkoncernen voestalpine AG med säte i österrikiska Linz och över 50 000 anställda. voestalpine High Performance Metals Sweden är Uddeholms säljbolag i Sverige.
Uddeholm är världens ledande tillverkare av verktygsstål för industriverktyg och finns i över 90 länder. Det är ingen tillfällighet. I varje stålbit, i varje steg av processen, från råmaterial till slutprodukt, satsar vi hela vårt hjärta. Tekniken är viktig, kunskapen och produktutvecklingen likaså, men det handlar också om viljan och modet, kraften och framåtandan. Det handlar om glöden inom oss – om kärleken till stålet! Visa mindre

Job description
The Clinical Supply Co-ordinator supports the Global Clinical Supply Chain teams to ensure the delivery of Clinical material and associated information to meet the agreed Clinical demand. The Clinical Supply Co-ordinator role covers parts of the clinical study lifespan, across all phases of the drug development lifecycle, covering small and large molecule drug products. 


The Global Clinical Supply Chain organisation are managing the supply chain for a portfolio of global clinical studies across all phases within a drug development programme. The Clinical Supply Study Lead and Clinical Supply Program Lead works in collaboration with customer functions to influence and manage demand for individual programs and studies and are responsible for their supply chain deliverables.


The Clinical Supply Co-ordinator is an important role in the Global Clinical Supply Chain organisation supporting the Clinical Study Supply Lead (CSSL) and Clinical Supply Program Lead (CSPL).

Responsibilities
The Clinical Supply Co-ordinator can support global Clinical Supply Study Lead teams with task based activities including:
Electronic Trial Master File documentation archiving
Temperature Control Monitor tracking
Activities related to manufacturing of drug substance, drug product and packaged supplies e.g: API order form creation and Bulk Drug order form creation
Smart Supplies forecasting
ANGEL documentation uploading
Pre and post batch record review and release for primary and secondary packing jobs incl. Links Reports and packing order creation 
Maintain supplies by proactively managing the demand, updating forecasts and executing plans.
Work with multiply customers and stakeholders internally and externally.
Capable to use IRT system for management of study material. 
Supporting RFQ updates with systems data
Invoice checking
Complaints management
Proactively co-ordinate close out activities including stock destruction, archiving etc.
Follow SHE and GMP standards and is personally accountable for these areas within own work plans.


Qualifications
Preferred Minimum Education/Experience:
Demonstrable Aptitude for systems (MS Office)
Proven customer service skills
Highly Organised
Proven ability to self-manage and motivate. 
Awareness of GMP standards
Awareness of Clinical Development processes relevant to the supply of clinical materials.
Problem-solving skills
Excellent written and verbal communication skills in both Swedish and English



Skills/Behaviours: 
Builds relationships - Takes actions for development of relationships with customers and stakeholders
Delivery Focus - Demonstrates focus, initiative and tenacity to achieve goals and objectives, using experience and judgment to make decisions and overcome barriers.
Customer Orientation - Develops and sustains collaborative customer relationships. Works in partnership with internal and external customers to deliver business benefits, seeking to understand their requirements.
Planning and Organizing – Schedules and optimizing the use of resources whilst considering the impact on others. Utilizes formal planning methodologies as appropriate.
Initiative - Engages in proactive behaviour, seeking and seizing opportunities to achieve business objectives and resolve issues.
Team Working - Actively participates as part of a team. Adapts role within team as required.
Flexibility - Adapts positively to changes in tasks or environment, maintaining enthusiasm and Effectiveness, regarding change as an opportunity for learning and growth.




Values and Behaviours:
We are Entrepreneurial:
 - I collaborate with colleagues internally and externally to seize opportunities and make decisions with speed.


We do the Right Thing:
 - I take personal accountability for my actions and for the success of AZ as a whole. 
 - I treat colleagues with respect and candor


We put Patients First: 
- I hold myself and others accountable for making decisions in the best interests of the patient. 

For us, it is important that all competence and skills in the labor market are utilized. We welcome all applicants and strive for diversity.

Application
 2019-11-07, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


For more information: Birgitta Nyström, Consultant manager, [email protected] or Kerstin Karlsson, Consultant manager, [email protected].

About the company
Randstad Life Sciences specializes in the field of science and is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! 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


Are you a dedicated and curious Stem Cell Scientist? Would you like to join us on our journey where your contributions will have a profound impact on R&D using the latest engineering techniques?


An exciting opportunity is now available for you to join our Stem & Primary Cell Team. We are part of the Discovery Sciences department, responsible for the generation of novel cellular models to support projects in all phases of the drug discovery pipeline. We have a focus on target identification, target validation, disease model generation and the therapeutic use of stem cells. 


You will be based in Gothenburg Sweden, where your main focus will be set on culturing, genetically engineering and differentiating stem cells for cellular model development and their potential use as therapeutics.


The role
Leveraging your strong knowledge and experience in stem cell biology and tissue culture you will have the opportunity to work with cutting edge cellular models of disease. This includes culture of induced pluripotent stem cells (iPSCs) as a platform for differentiating to disease relevant cellular lineages relevant to the diseases and conditions that are the focus of research at AstraZeneca Gothenburg. 


The role is focused on laboratory-based activities, applying your knowledge and skills to drive project delivery, participate actively in problem solving and, where relevant, deliver cross disciplinary support based on your experience. Your biggest impact will be through significant contributions to the practical delivery of projects in compliance with AstraZeneca corporate responsibility policies and relevant safety standards.


It is essential to have good social and communication skills, be collaborative and a strong team player. Candidates should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude. Good organisational, data management and documentation skills are required, and you should be comfortable in presenting your results. English language is required, both spoken and in writing.

Responsibilities
Tasks
To culture iPSCs to generate cellular models of human disease biology
To apply existing differentiation protocol, and where relevant contribute to development of new protocols, to deliver cells and cellular models for drug discovery activities.


Qualifications
The following skills are highly desirable:
Experience in iPSC culture and quality control
Application of differentiation protocols for generation of complex stem-cell based cell models
Qualification and validation of cellular models using imaging techniques
Molecular Biology and Cell line engineering


Minimum experience:
For the Research Scientist role, you should hold a B.Sc. or M.Sc. degree with corresponding experience in a relevant scientific discipline with experience in cell culture.


For the Senior Research Scientist role, you should either hold a Ph.D. in Cellular Biology or a related degree or have significant relevant experience working in a cell culture Environment.

Application
2019-11-19, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


For more information: Contact Galia Nyström, Consultant Manager, [email protected] or Kerstin Karlsson, Consultant Manager, [email protected]. 

About the company
Randstad Life Sciences specializes in the field of science and is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in life science. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Job description
There is an attractive opening for a master student to join AstraZeneca's In vitro Biochemical Assays team, for developing high throughput assays for studying PROTAC-mediated protein degradation. PROTACs (Proteolysis targeting chimera) have emerged as an important new modality in drug discovery with the potential to deliver the next generation of medcines. We are interested to explore novel in vitro assays for understanding the mechanism of PROTAC-mediated protein degradation. 


AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. Our Discovery Sciences team operates from truly state-of-the-art centre in Sweden. You’ll work with some of the most knowledgeable technological experts in the industry, all collaborating on high-profile drug discovery projects. We’re also early adopters of new technologies to support innovation, including CRISPR, genome editing techniques, PROTACs, transcriptomics and next-generation sequencing.


On a daily basis you will work in the In vitro Biochemical Assays team with colleges/experts working on developing high throughput biochemical assays using state-of-the-art technologies to support drug discovery projects. You will be developing a project integrated in their current research activities benefiting from daily support from an experienced supervisor. 

Responsibilities
In this project you will learn about the new concept of PROTAC (Proteolysis targeting chimera) modality of medicine, and have the opportunity to explore world-leading science and develop different in vitro high throughput assays for studying the mechanism of PROTAC-mediated protein degradation. During this period you will gain extensive experience in developing high throughput in vitro assays to study the mechanism of PROTACs. You will gain practical independency in techniques/skills such as experimental design, cell culturing, Western blotting, advanced assay technologies such as TR-FRET, NanoBBRET and Nano-Glo assays, high throughput assay development, assay validation tools, and thesis writng. You will be independently conducting laboratory work, analysing the data collected and organizing it into scientific presentations to your peers, and you will have the opportunity to actively and critically participate in the development of the project. 

Qualifications
Essential requirements:
A bachelor in biological sciences with a strong cell biology or biochemical focus.
Excellent organizational, communication and interpersonal skills, combined with the ability to work collaboratively across boundaries and problem solve in the absence of complete information.
Excellent communication skills in English (speaking, presenting and writing).



Desirable requirements:
Basic knowledge around handling mammalian cell culture
Experience working in a biochemical laboratory


Application
Deadline for application: 2019-11-17, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


 For more information: Kerstin Karlsson [email protected] or Eleonor Ehrman +4673-343 41 09.

About the company
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.


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, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised. Visa mindre

Job description
Thesis work: 60 credits/spring and autumn 2020
Increasing CRISPR/Cas9-mediated knock-in efficiency in human induced pluripotent stem cells

Do you have a passion for cell and molecular biology? Would you like to learn more about CRIPSR/Cas9 and its application in gene therapy? Then AstraZeneca might be of interest to you!


We have an exciting opening for a master student in our Precise Genome Editing team. The Discovery Sciences department is responsible for generation of novel genome editing technologies to support projects in all phases of the drug discovery pipeline. Our focus is set on target identification, target validation, disease model generation and the therapeutic use of stem cells.

Responsibilities
Low efficiency of knock-in events represents a major obstacle in the therapeutic use of CRISPR/Cas9. Yet, the interplay between CRISPR/Cas9 systems and eukaryotic DNA damage repair (DDR) pathways is poorly understood.


The candidate will get the opportunity to work on a project to improve the efficiency of Cas9-mediated knock-ins in eukaryotic cells. You will evaluate the potential of compounds targeting DNA repair factors to enhance the efficiency of genome editing at different target-sites in diverse cell-lines including human induced pluripotent stem cells (hiPSC). 


Core tasks:
Gain expertise in designing and performing genome editing experiments using CRISPR/Cas9
Learn how to culture hiPSC 
Next generation sequencing data generation, analysis and interpretation
Basic programming in VBA 


Qualifications
Essential Requirements:

We are looking for a motivated master student with a background in biology/biotechnology that is willing to learn a broad range of biochemical, cellular and molecular biology techniques.


Your social and communication skills are essential as well as your ability to work in teams.

Desirable Requirements:

Knowledge of basic cellular and molecular biology techniques including cell culture, transient transfection and cloning would be advantageous.


If you are interested, apply now!



Application
Deadline for application: 2019-11-17, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.

For more information: Kerstin Karlsson [email protected] or Eleonor Ehrman +4673-343 41 09.



About the company
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.

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, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised. Visa mindre

Job description
Thesis work: 60 credits/spring and autumn of 2020


We have an attractive opening for a Master student to join our exosome team. Exosomes are extracellular vesicles released by virtually every cell in our body. They contain RNA, DNA and proteins and are important players in cellular communication. At AstraZeneca, we are interested in exploring exosomes as natural vehicles for drug delivery. 


AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. You will be joining our Discovery Sciences function, that operates from a truly state-of-the-art centre in Sweden. Here, you will work side-by-side with some of the most knowledgeable technological experts in the industry, all collaborating on high-profile drug discovery projects. We are also early adopters of new technologies to support innovation, including CRISPR, genome editing techniques, transcriptomics and next-generation sequencing.

On a daily basis you will work in the Exosome Team with colleagues developing engineered exosomes for improved delivery of therapeuthical protein and RNA drugs in vitro and in vivo. We have developed an extensive expertise in the field since 2016 and our research have been resulting in high impact publications over the years (Heath et al., Sci. Rep., 2018; Saleh et al., Nanoscale, 2019). You will be developing a project integrated in our current research activities benefiting from daily support from an experienced supervisor. 

Responsibilities
In this project you will have the opportunity to explore world-leading science and develop different in vitro systems to improve the efficiency of loading of RNA drugs, like microRNAs, siRNAs and CRISPR/sgRNAs into exosomes, via RNA modification/engineering. During this period you will gain extensive experience in exosomes production and characterization, mammalian cell culture and engineering, RNA engineering, and cell-reporter and functional delivery assays, and will gain practical independency in techniques such as western blotting, nanoparticle tracking analysis, cell transfection, digital PCR, cell imaging, among others. You will be independently conducting laboratory work, analysing the data collected and organizing it into scientific presentations to your peers, and you will have the opportunity to actively and critically participate in the development of the project. 

Qualifications
Essential requirements:


A bachelor in biological sciences with a strong cell biology or biochemical focus.
Excellent organizational, communication and interpersonal skills, combined with the ability to work collaboratively across boundaries and problem solve in the absence of complete information.



Desirable requirements:


Basic practical knowledge handling mammalian cell culture.
Basic practical knowledge of molecular biology techniques.
Experience working in a biochemical laboratory.


Application
Deadline for application: 2019-11-17, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.


 For more information: Kerstin Karlsson [email protected] or Eleonor Ehrman +4673-343 41 09.

About the company
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.

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, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised. Visa mindre

Arbetsbeskrivning
Vi söker dig som ser lösningar där andra ser hinder!

Piab Ergonomic Handling Division utvecklar och producerar bl.a. Vaculex produkter som är världsledande inom lyftsystem baserade på vakuumteknik. Under de senaste 30 åren har Vaculex helhetslösningar levererats inom många branscher med höga krav på ergonomi, säkerhet och effektivitet. Produktutveckling, konstruktion och tillverkning sker i vår egen regi och vår personal är innovativ och har stor drivkraft.  Vi tillverkar kundanpassade lösningar som ställer höga krav på vår supportorganisation och nu behöver vi en ersättare till gruppen eftersom en kollega går på föräldraledighet, vill du bli en av oss? 

Ansvarsområden
Som Supportingenjör hos oss kommer du arbeta nära vår säljorganisation för att utveckla och anpassa våra produkter utifrån våra kunders behov. Du arbetar med allt från enklare beräkningar, skapar offertunderlag och är teknisk rådgivare till kunder och kollegor.  Andra arbetsuppgifter som förekommer är t. ex. ritningar i 3D, problemlösning för kundsupport, delaktig i framställning av manualer och dokumentation, utvecklar processer samt deltar i andra förekommande arbetsuppgifter på avdelningen. 

Hos oss erbjuds du möjligheten att använda din tekniska kunskap och problemlösningsförmåga för att utveckla och förbättra våra produkter efter kunds behov. Vill du fortsätta att utvecklas som person i en tekniskt stöttande roll är detta tjänsten för dig!

Piab är ett innovativt bolag där beslutsvägarna är korta och trivsamheten hög. Du kommer att arbeta i ett framgångsrikt och expansivt företag i en växande bransch. Du rapporterar till Sales Support Manager med placering på vårt kontor på Aminogatan 20 i Mölndal. 

Kvalifikationer
Du har ett tekniskt intresse och gärna arbetslivserfarenhet från en liknande roll samt en förmåga att arbeta båda självständigt och i projektform. Du gillar att ge service och support samt att se till att allt dokumenteras på rätt sätt för fortsatta processer. Du arbetar gärna nära försäljningsavdelningen, utvecklingen och våra kunder för att lösa deras behov.

För att vara framgångsrik i rollen tror vi att du har en teknikbakgrund med inriktning från t.ex. maskin, automation eller liknande. Du har lätt för att kommunicera teknik till olika personer, har körkort samt goda kunskaper i svenska och engelska i tal och skrift. Rätt person är serviceinriktad, lösningsfokuserad, har en rådgivande och positiv attityd. Du har stort tekniskt intresse och är praktiskt lagd. Du har social kompetens och hanterar stressiga situationer på ett strukturerat och organiserat sätt. Hos Piab är din öppenhet och positiva syn på utveckling en nyckel till framgång.

Ansökan
Ansök med CV så snart som möjligt. I denna rekrytering kommer du att anställas som konsult via Randstad Engineering, men arbeta ute på plats hos Piab. Uppdraget ligger initialt på ett år, med goda möjligheter till ett övertag eller att fortsätta med en karriär inom Randstad Engineering. Vid frågor om tjänsten så är du varmt välkommen att kontakta konsultchef Rebecka Simonsson via mail [email protected].

Uppdragsgivare: Randstad Engineering

Omfattning: Heltid, tillsvidare

Ort: Göteborg

Sista ansökningsdag: 2019-11-18, urval och intervjuer kommer att ske löpande. Tjänsterna kan komma att bli tillsatt innan sista ansökningsdag, ansök därför så snart som möjligt.



Om företaget
Piab erbjuder smarta lösningar för en automatiserad värld och hjälper tusentals slutanvändare och maskintillverkare inom e-handelslogistik, livsmedel, läkemedel, bilindustri och andra tillverkningsindustrier med att förbättra energieffektivitet, produktivitet och arbetsmiljö. Piab är en global organisation som har dotterbolag och distributörer i närmare 70 länder, närmare 500 anställda och drygt 1,2 miljarder kronor i försäljning 2018. Genom att dra fördel av den pågående teknikutvecklingen inom automatisering och robotisering, och rikta in sig mot snabbväxande segment och geografier, är Piabs vision att bli den globala ledaren inom robotiserade grip- och förflyttningslösningar.

Ergonomic Handling Divisionen utvecklar och producerar produkter som är världsledande inom lyftsystem baserade på vakuumteknik. Vår utveckling och produktion finns i Mölndal på Aminogatan 20. Välkommen till oss! Läs gärna mer om oss på:  www.piab.com. Visa mindre