Lediga jobb som Forskningschef i Mölndal

Är du en trygg och inspirerande ledare som drivs av utmaningar? Tycker du att samarbete över teknik- och verksamhetsområden är en självklarhet för skapandet av både nya affärer och nya innovationer? Vill du hjälpa svensk industri att bibehålla och stärka sin konkurrenskraft, såväl nationellt som internationellt?
Vi söker en erfaren ledare till avdelningen Metodik, textil och medicinteknik med placering i Borås eller Mölndal.
Om oss
RISE är en kraftsamling för den hållbara omställning näringslivet, samhället och världen behöver. Som hela Sveriges forskningsinstitut jobbar vi med lösningarna och förutsättningarna som gör skillnad här och nu och med de kunskapsområden och tekniker som kan vara avgörande imorgon.
Divisionen Material och produktion samlar expertis inom forskningsområden med fokus på utveckling av material, produktion och produkter för tillverkningsindustrin inom en mängd olika branscher. Vårt erbjudande byggs upp av unik infrastruktur i form av test- och demonstrationsanläggningar och labb i kombination med djup kompetens inom såväl relevanta teknikområden som hållbarhet och digitalisering, med syftet att vara en nyckelspelare i industrins omställning och totalförsvarets uppbyggnad.
Inom avdelningen Metodik, textil och medicinteknik drivs utveckling och utvärdering av material, processer och produkter inom olika områden, som life science, textil och metall. Fokus är också på utveckling av erbjudanden inom coachning och rådgivning, metodutveckling. Expertis finns inom innovationsledning, produktionseffektivitet, miljö och hållbarhet, kemisk substitution, industriell digitalisering och interaktioner med biologiska system. Avdelningen består av sex enheter med drygt 120 engagerade medarbetare. Verksamheten bedrivs på tre platser i Sverige, Stockholm, Mölndal/Göteborg och Borås. Om rollen
Som avdelningschef ansvarar du för att stärka avdelningens och RISE innovationsförmåga och utveckling. Det gör du i samverkan med kollegor inom hela koncernen och tillsammans med våra kunder samt partners. Tillsammans med din ledningsgrupp definierar ni den strategiska inriktningen och möjliggör den dagliga verksamheten för våra medarbetare. Du involverar och coachar enhetscheferna i deras uppgift att bryta ner det övergripande uppdraget i verksamheten och säkra våra medarbetares leverans och utveckling.
Du rapporterar till Divisionschef och ingår i divisionsledningen för Material och produktion och du har medarbetar-, budget- och utvecklingsansvar för din avdelning. Du arbetar nära våra kunder och du hjälper oss att vidareutveckla RISE olika erbjudanden. Som avdelningschef hos oss leder och agerar du utifrån vår kultur och våra värderingar och är en viktig ambassadör för RISE. Du arbetar i en framåtblickande och innovativ miljö där samverkan och modigt ledarskap är stora framgångsfaktorer. Vem är du?
För att bli framgångsrik i rollen är du en erfaren ledare som trivs med förändringsledning. Du är trygg i ditt ledarskap och coachar medarbetare i rätt riktning för att säkra att ni tillsammans på ett engagerande och professionellt sätt presterar och bidrar till utveckling. Du är lyhörd och kommunikativ samt jobbar aktivt för att skapa en trygg och tillitsfull arbetsmiljö. Du är nyfiken och intresserad av olika domänområden och hur de kan samverka för att föda innovation, stärka forskningen och vår test- och demo verksamhet samt öka vårt kommersiella fokus. Vidare är du affärsmässig och inger stort förtroende hos såväl kunder som medarbetare. Du har en god samarbetsförmåga och motiveras av att växa tillsammans med andra.
Som chef på RISE är du en modig och visionsdriven ledare med ett tydligt fokus på resultat och samverkan. Du tar initiativ och leder med självförtroende både i vardagliga beslut och i komplexa utmaningar. Vi söker dig som är redo att möta spännande utmaningar och leda med både mod och vision i en dynamisk och innovativ miljö.
Krav för rollen:
Du har omfattande ledarskapserfarenhet och har aktivt deltagit i ledningsgrupper för att driva strategiska beslut och utveckling, samtidigt som du har haft ansvar för att leda andra chefer.
Kunskap och erfarenhet av att leda en verksamhet med ekonomisk styrning, personal- och budgetansvar
En bred och mångfacetterad bakgrund inom både näringslivet och den offentliga sektorn, gärna med erfarenhet av att leda forsknings- och utvecklingsorganisationer
Du har relevant universitetsutbildning
Flytande svenska och engelska i tal och skrift

Meriterande för rollen:
Branscherfarenhet inom områden som produktion, life science, textil och hållbarhet

Välkommen med din ansökan!
Är du intresserad och vill veta mer så är du välkommen att kontakta rekryterande divisionschef Pernilla Walkenström 010 516 62 88 [email protected]. Sista ansökningsdag är den 18:e april 2025.
Urval och intervjuer kommer ske löpande under ansökningstiden. Våra fackliga representanter är Ingemar Petermann, SACO, +46 10 228 41 22 och Linda Ikatti, Unionen, +46 10 516 51 61.
Befattningen kan komma att bli placerad i säkerhetsklass, vilket innebär att du kan behöva genomgå en säkerhetsprövning, i enlighet med säkerhetsskyddslagen nu eller längre fram. Visa mindre

Job description
Supply Chain Manager for Clinical Trial medications
Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.
We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca’s trials all over the world. Our goal is to never miss a patient.


In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.
What you'll do In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.


To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.


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

Responsibilities
Your main responsibilities will include:
Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
Ensure effective communication with project teams and key partners across a global network.
Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.


Qualifications
Essential for the role:
Experience within a Supply Chain Management environment with a holistic knowledge of end-to-end supply chain activities (minimum 2 years experience desirable)
Proficient IT skills with an ability to adapt and operate in bespoke multiple systems
Experience in running projects and in?uencing customer demands
Experience of demand planning and forecasting and risk identification and management
Excellent English written and verbal communication skills



Desirable for the role:
Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
Knowledge of clinical development processes relevant to the supply of clinical materials
Lean knowledge and understanding
Experienced in handling Quality Events (Deviations, Change Controls, Complaints)
Knowledge of clinical development processes relevant to the supply of clinical materials
Working in a leading role within a team


About the company

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

Job description
Supply Chain Manager for Clinical Trial medications


Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.
We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca’s trials all over the world. Our goal is to never miss a patient.
In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.


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

Responsibilities
What you'll do


In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.
To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.


Your main responsibilities will include:
• Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
• Ensure effective communication with project teams and key partners across a global network.
• Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
• Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
• Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
• Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.

Qualifications
Essential for the role:
• Bachelor’s Degree in Supply Chain, business or scientific subject area – equivalent experience within Supply Chain will be considered
• Experience within a Supply Chain Management environment with a holistic knowledge of end-to-end supply chain activities (minimum 2 years experience desirable)
• Proficient IT skills with an ability to adapt and operate in bespoke multiple systems
• Experience in running projects and in?uencing customer demands
• Experience of demand planning and forecasting and risk identification and management
• Excellent English written and verbal communication skills


Desirable for the role:
• Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Lean knowledge and understanding
• Experienced in handling Quality Events (Deviations, Change Controls, Complaints)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Working in a leading role within a team

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

Would you like to work as a Clinical Project Manager in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A place that is constantly moving forward, with great science, great people, and an informal atmosphere? Do you enjoy reaching goals in a fast-paced environment through teamwork and collaboration? If this ticks your boxes, you should continue reading.

At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET), to design and deliver clinical studies for decision making and differentiation in drug development.

We value competence and development as well as ideas and creativity. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 90 employees working at our offices in Sweden in Mölndal and Uppsala, as well as a newly established subsidiary in the US, and we are continuously growing and developing.

As a part of our growth journey, we are looking for our next Clinical Project Manager with experience in clinical drug development. You will ideally join our office in Mölndal or Uppsala in Sweden, with flexibility to partly work home-based. The position could possibly be placed internationally home-based in the US or Europe.

As a Clinical Project Manager at Antaros Medical, you will be overall responsible and accountable for project management of the imaging part in clinical trials, from initiation to end of assigned projects. Your responsibility includes to ensure the projects are delivered accordingly with timelines, to the agreed budget, with high quality, and per internal and client’s SOPs, ICH/GCP and other regulation.

Your main responsibilities will be:

- Manage multiple projects ranging in size and complexity, from single to multicenter studies
- Act as a primary contact to the client to ensure smooth operations and communication
- Manage the internal trial team to ensure the right input at the right time from different skills within the company
- Present project information at internal and external meetings
- Risk management responsibility and lessons learned for assigned projects
- Manage the project financials in collaboration with the Finance Department and financial follow-up for assigned projects


Who are we looking for?

We believe that you have demonstrated collaboration skills as well as a team-oriented approach to engage with colleagues and clients. You have the flexibility and the ability to handle multiple tasks and projects to meet deadlines while delivering high-quality work in a dynamic environment.

As a person, we further believe that you are outgoing and enthusiastic, a natural communicator, and can adapt your approach depending on the situation. You work as a team player and apply communicative and interactive skills on different levels within the organization and with external parties and customers.

Requirements:

- University degree in Life Science
- At least 3 years’ experience from working with clinical trials from start to end of projects
- Experience within project management of clinical trials is meritorious
- Strong understanding of ICH-GCP and other relevant regulations and guidelines in relation to clinical trials
- Understanding of the full drug development process
- Excellent written and verbal communication skills in Swedish and English


Are you interested?

Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than 18th July, 2021.

For more information about the position, please contact Richard Olbe, Manager Clinical Operations, at +46 732301011.

About Antaros Medical

At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialised in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicines Initiative (IMI) and COST.

Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com (http://www.antarosmedical.com/) Visa mindre