Development Scientist within Stability for API Manufacturing Development
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Do you have experience with protein chemistry? Are you motivated by and have experience in working with stability studies, production support and regulatory documentation? Are you eager to learn and kick-start your career at Novo Nordisk or do you bring a solid experience and are ready for a more senior position?
Then you might be our new Development Scientist within Stability in API Process Support.
The position
Together with your team colleagues, your main focus will be to act as point of entry for our numerous stakeholders. As product responsible, you will assess the need for stability studies; both when new processes are transferred from development to production and as part of production process optimisation. Moreover, you will support the production with stability data in compliance with Good Manufacturing Practice (GMP). On a daily basis, your main tasks will be to design stability studies, write protocols, reports and regulatory documents, perform trend evaluation of data and comment on deviations related to the stability of the products. Based on your seniority-level, the position will be adjusted accordingly.
Qualifications
As a person you,
About the department
You will become a part of API Process Support, which is a department in our Active Pharmaceutical Ingredient (API) Manufacturing Development. Our main responsibility is to ensure that manufacturing processes are continuously optimised and new processes are transferred from development to production.
The department is located in Bagsværd and consists of 80 employees organised in five teams. We play a central role in supporting the production of API and have many other stakeholders, including Quality Control, Quality Assurance, Senior Project Managers, and Regulatory Affairs. Within the department, you will be a part of the stability team, consisting of 6 chemists and 6 laboratory technicians. Here, our focus is stability testing of both new as well as marketed drug substances.
We are known for an open-minded and cooperative working environment, and we believe that it should be both scientifically exciting and fun to go to work.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
If you have questions you need answered before applying, please feel free to call Claus Juul-Mortensen at +45 30759732.
Should you wish to learn more about working at Novo Nordisk, here is a good place to begin: https://www.novonordisk.com/careers/working-at-novo-nordisk.html
Deadline: November 24st, 2022
Applications will be reviewed on an ongoing basis, so please do not hesitate to apply.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your 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.
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Then you might be our new Development Scientist within Stability in API Process Support.
The position
Together with your team colleagues, your main focus will be to act as point of entry for our numerous stakeholders. As product responsible, you will assess the need for stability studies; both when new processes are transferred from development to production and as part of production process optimisation. Moreover, you will support the production with stability data in compliance with Good Manufacturing Practice (GMP). On a daily basis, your main tasks will be to design stability studies, write protocols, reports and regulatory documents, perform trend evaluation of data and comment on deviations related to the stability of the products. Based on your seniority-level, the position will be adjusted accordingly.
Qualifications
- You hold a M.Sc. degree or higher in Pharmacy, Biochemistry, Chemical Engineering or other relevant scientific discipline.
- You have experience within protein chemistry, data analysis, and at least some experience with statistics (e.g. SAS Jump).
- You have experience within the pharmaceutical industry, as well as experience from working in a GMP environment. You will be in daily contact with chemists, technicians, production employees, project managers, analytical laboratories and other stakeholders. Therefore, it is important that you are a strong communicator and that you master Danish and English both orally and in writing.
As a person you,
- exhibit a positive nature enabling you to build fruitful relations to stakeholders and respond constructively to challenges.
- You are a person who thrive in – and contribute to - a working environment where a good laugh is appreciated even when things occasionally get hectic.
- You have a strong quality mind-set and focus on meeting deadlines by prioritising your work assignments and helping your colleagues.
About the department
You will become a part of API Process Support, which is a department in our Active Pharmaceutical Ingredient (API) Manufacturing Development. Our main responsibility is to ensure that manufacturing processes are continuously optimised and new processes are transferred from development to production.
The department is located in Bagsværd and consists of 80 employees organised in five teams. We play a central role in supporting the production of API and have many other stakeholders, including Quality Control, Quality Assurance, Senior Project Managers, and Regulatory Affairs. Within the department, you will be a part of the stability team, consisting of 6 chemists and 6 laboratory technicians. Here, our focus is stability testing of both new as well as marketed drug substances.
We are known for an open-minded and cooperative working environment, and we believe that it should be both scientifically exciting and fun to go to work.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication, and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
Contact
If you have questions you need answered before applying, please feel free to call Claus Juul-Mortensen at +45 30759732.
Should you wish to learn more about working at Novo Nordisk, here is a good place to begin: https://www.novonordisk.com/careers/working-at-novo-nordisk.html
Deadline: November 24st, 2022
Applications will be reviewed on an ongoing basis, so please do not hesitate to apply.
To ensure an efficient and fair recruitment process, please refrain from adding a photo in your 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.
Print job Send to e-mail
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 8.11.2022, 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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