Purification Scientist
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Gentofte
Are you ready to make a difference for people living with haemophilia and other rare diseases? Do you want to work with life cycle management of API processes in Biotech & Rare Disease (BRD)? Thus, being a vital part in securing treatments to chronic patients worldwide.
BRD’s portfolio is expanding, and we are therefore looking for an additional purification scientist at our Novo Nordisk site in Gentofte to support API production in the BRD area.
The position
As a purification scientist in our LCM API team, you will be involved in supporting different API productions within our BRD portfolio with downstream processes. You will work closely with API coordinators who represent our department, BRD API Manufacturing Development, in the product project teams and coordinate the relevant deliveries throughout the organization.
Your major tasks will include:
• Creating and maintaining central process and control documents such as master formulas, in-process control documents, risk assessments and drug substance quality specifications.
• Developing a drug substance stability strategy for ongoing stability.
• Providing support to solve and prevent issues in the API production sites in Gentofte, Hillerøg, Kalundborg, and the US.
• Ensuring compliance with regulatory files and answering questions from the authorities.
• Setting up yield and process optimization studies in our in-house laboratory
You will collaborate with a wide range of stakeholders across Novo Nordisk, including production departments, Quality Assurance, development, Regulatory Affairs, analytical departments and project groups across development and BRD. Qualifications
To succeed in this position, you have:
• An academic degree within a scientific field such as biotechnology, chemistry, engineering or similar.
• At least 5 years of experience working with protein purification.
• Experience in pharmaceutical production.
• Experience with project management or/and stakeholder management.
• Full professional proficiency in oral and written English.
Strong communication and collaboration skills are crucial to ensure efficient distribution of tasks and alignment across the team, the department and within BRD. You should be outgoing and self-driven as a person. Additionally, you should thrive in an environment where you get to throw yourself in at the deep end, always seizing an opportunity for personal and professional development.
BRD is expanding rapidly, and the project plans are ambitious, which means that you should enjoy the fast pace and be pragmatic to finding the correct level in your professional tasks to live up to requirements while also supporting the business needs. About the department Manufacturing Development is a part of BRD with a team of over 650 colleagues working together to optimise and develop processes across six global production sites. Our field of work broadly covers the area also known as MSAT (Manufacturing, Science, and Technology). We bring value to our patients by driving innovation for the entire BRD, working with Industry 4.0, new technologies, biotechnology, and developing processes for both existing and future products.
Working at Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology.
Contact If you have any questions about the position, please do not hesitate to contact Manager Helle Damgaard Nielsen [email protected].
Deadline
4 February 2024. We will review applications and conduct interviews on an ongoing basis, so you are encouraged to apply as soon as possible.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
BRD’s portfolio is expanding, and we are therefore looking for an additional purification scientist at our Novo Nordisk site in Gentofte to support API production in the BRD area.
The position
As a purification scientist in our LCM API team, you will be involved in supporting different API productions within our BRD portfolio with downstream processes. You will work closely with API coordinators who represent our department, BRD API Manufacturing Development, in the product project teams and coordinate the relevant deliveries throughout the organization.
Your major tasks will include:
• Creating and maintaining central process and control documents such as master formulas, in-process control documents, risk assessments and drug substance quality specifications.
• Developing a drug substance stability strategy for ongoing stability.
• Providing support to solve and prevent issues in the API production sites in Gentofte, Hillerøg, Kalundborg, and the US.
• Ensuring compliance with regulatory files and answering questions from the authorities.
• Setting up yield and process optimization studies in our in-house laboratory
You will collaborate with a wide range of stakeholders across Novo Nordisk, including production departments, Quality Assurance, development, Regulatory Affairs, analytical departments and project groups across development and BRD. Qualifications
To succeed in this position, you have:
• An academic degree within a scientific field such as biotechnology, chemistry, engineering or similar.
• At least 5 years of experience working with protein purification.
• Experience in pharmaceutical production.
• Experience with project management or/and stakeholder management.
• Full professional proficiency in oral and written English.
Strong communication and collaboration skills are crucial to ensure efficient distribution of tasks and alignment across the team, the department and within BRD. You should be outgoing and self-driven as a person. Additionally, you should thrive in an environment where you get to throw yourself in at the deep end, always seizing an opportunity for personal and professional development.
BRD is expanding rapidly, and the project plans are ambitious, which means that you should enjoy the fast pace and be pragmatic to finding the correct level in your professional tasks to live up to requirements while also supporting the business needs. About the department Manufacturing Development is a part of BRD with a team of over 650 colleagues working together to optimise and develop processes across six global production sites. Our field of work broadly covers the area also known as MSAT (Manufacturing, Science, and Technology). We bring value to our patients by driving innovation for the entire BRD, working with Industry 4.0, new technologies, biotechnology, and developing processes for both existing and future products.
Working at Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology.
Contact If you have any questions about the position, please do not hesitate to contact Manager Helle Damgaard Nielsen [email protected].
Deadline
4 February 2024. We will review applications and conduct interviews on an ongoing basis, so you are encouraged to apply as soon as possible.
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Gentofte.
Jobbet er oprettet på vores service den 16.1.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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Statistik over udbudte øvrige i Gentofte over tid
| Dato | Alle jobs som øvrige |
|---|---|
| 4. november 2024 | 19 |
| 3. november 2024 | 19 |
| 2. november 2024 | 19 |
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| 6. oktober 2024 | 23 |
| 5. oktober 2024 | 23 |