Chemist with flair for Stability

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Are you motivated by working with stability studies, production support, regulatory documentation, and data science? Do you have an innovative mindset towards digital automation of e.g. paper-based processes? Then you might be the new colleague we are looking for in our dedicated API Manufacturing Development Stability team. The job 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. As Chemist your primary daily tasks will include:
  • Supporting the production with stability data in compliance with Good Manufacturing Practice (GMP).
  • 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.
    • In addition to these day-to-day tasks, we want to start projects with focus on digital automation/statistic both in the team and the department. Here we see you as a contributor to drive and executer the different projects. Qualifications To be successful in this role it is required that:
  • You hold a M.Sc. degree or higher in Pharmacy, Biochemistry, Chemical Engineering or other relevant scientific discipline preferably with skills in the area of stability.
  • You have vast experience within protein chemistry and data analysis, and you exhibit an interest in statistics.
  • Preferably, 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 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. In addition, 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 PS API organisation, MDev 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 100 employees organised in six teams. We play a central role in supporting the production of Diabetes 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 7 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 collaborative working environment, and we believe that it should be both scientifically exciting and engaging to go to work. About Novo Nordisk At Novo Nordisk, your skills, commitment and ambitions help us to improve the lives of millions. 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 For further information, please contact Claus Juul-Mortensen at +45 3075 9732. Deadline January 14, 2024 Applications will be reviewed 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. 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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    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 29.12.2023, men kan have været deaktiveret og genaktiveret igen.

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