Contract Manufacturing Specialist (Drug Substance Production)

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Are you looking to bring your pharmaceutical experience to an international level in a global business environment? Do you have experience in pharmaceutical chemistry production? Would you thrive in implementing new production and influence and improve existing processes and conditions profoundly? If so, then apply today as you might be the person our Global Contract Manufacturing (GCM) Team is looking for! The Position As Contract Manufacturing Specialist (Drug Substance Production) you will work with CMOs (Contract Manufacturing Organisations) that produce side-chains, intermediates and drug substance that subsequently will be supplied to Novo Nordisk for further production. The main work responsibility is to be the responsible specialist of API or intermediate manufacturing in project teams with a special focus on facility, equipment and QMS. In this position, you will:
  • Author and review project documentation, validation reports, master batch records, change requests etc.
  • Be the technical process equipment facility specialist
  • Be a part of an experienced project team that is put together cross-functionally
  • Gain knowledge of the production through the project work, including the chemistry behind the process, the production equipment, the facility and other processes related to the manufacture
  • Act as knowledgeable specialist in daily operation when production issues occur
    • We expect you to make procedural or process suggestions for achieving team goals or performing team functions; providing necessary resources and help to remove obstacles, ensuring the team accomplishes specific results. As our new Contract Manufacturing Specialist (API/side-chain expert drug substance), you will quickly become a visible beacon of knowledge across and beyond a truly global organisation. Several of the CMOs we currently work with are in project phases where extra focus is needed from a set of skilled specialists. Possibility of remote working included (1-2 days per week). Qualifications You will be part of several teams – both formally and informally – why the ability to work across boundaries is critical for your success.
  • Master’s Degree within a relevant area, e.g. Chemistry, Pharmacy, Engineering or similar
  • Theoretical background is combined with at least eight years of practical experience within the pharmaceutical industry and manufacturing of pharmaceutical products under GMP
  • You should be able to demonstrate knowledge of API/side-chain production within the areas where Novo Nordisk is active, e.g. synthetic chemistry, protein production, peptide production, fermentation etc.
  • Knowledge within quality control laboratory is also a merit
  • You have an analytical mind-set with the ability to work in a structured way and an ability to support multiple activities
  • Experience from an international environment will make it easier for you to build results quickly
  • Strong communication skills in the English language
    • As a person you are good at building trust with stakeholders, and you naturally share important and relevant information with your team. Working location will be in Bagsværd and since international collaboration is an integrated part of your job, you can expect to be travelling around 25 days per year. About the Department Global Contract Manufacturing (GCM) is part of Novo Nordisk’s Product Supply organisation. We are responsible for all Novo Nordisk contracts and licence manufacturing of Active Pharmaceutical Ingredients (API’s), intermediates, semi-finished and finished drug products to global markets. Our main office is located in Bagsværd, Denmark. The primary role of GCM is to monitor and control the production handled by external Contract Manufacturing Organisations (CMOs), ensuring delivery of products from the CMOs to our respective customers. Our CMOs are located in Central Europe, North America and in East Asia. The position is in a production support department, Global Contract Manufacturing Support, a team of highly experienced specialists with a well-documented history in pharmaceutical sciences. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Thomas Lindblad, Director, Global Contract Manufacturing Support /+45 3075 5179. Deadline 10.04.2023. 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 14.3.2023, men kan have været deaktiveret og genaktiveret igen.

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