Drug Product Development Scientist

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Drug Product Development Scientist Do you have what it takes to break new land and develop injectable biopharmaceutical products during clinical development? Are you eager to act in a team linking research and production during clinical development and documentation of formulations and processes for new injectable products? If yes, then apply now! About the department Injectable Formulation Development is part of CMC Development. We are responsible for developing drug product formulations and production processes for injectables of new biopharmaceutical products. In our daily work we link research to pilot production and drive the entire variety of injectable projects from early stage (phase 1-2) to late-stage (phase 3-PPQ) development. The development projects in the department include e.g. GLP-1 products, insulins, haemophilia products, monoclonal antibodies, and RNAi. The position As our new Scientist, you will have the responsibility for product and process development to secure optimal pharmaceutical characteristics and stability. The open position is in the late phase development where the primary focus is development and manufacture of Drug Product for phase 3 clinical trials to market. The variety of tasks covers all related aspects of product development and related fields. With your achieved knowledge, you will therefore become a key person to secure continuous progress with our stakeholders. Your responsibilities will include:
  • Working in close collaboration with a project team, and be responsible for designing, interpreting, and reporting studies on drug products
  • Writing documentation for internal and external use including clinical trial applications and patent applications
  • Interacting with a wide variety of internal stakeholders, e.g., Production, Regulatory Affairs, Quality Assurance and Analytical Development
    • Together with our colleagues, you will also contribute to the on-going optimisation of processes and systems with LEAN as the guiding principle. Qualifications Our ideal candidate has the below qualifications:
  • You hold a M.Sc. or PhD within Pharmacy, Chemistry, Biophysics, Engineering of related field of study.
  • Experience in either formulation development, aseptic manufacturing process development, pharmaceutical production, or other relevant area within pharmaceutical drug products
  • Experience with documentation including regulatory and quality aspects of pharmaceutical drug products
  • Ability to promote collaboration with other parts of the organisation as the position requires close interaction with a variety of stakeholders
  • Possess strong communication skills both verbally and written in English
    • We are looking for someone who can show drive and have a positive can-do mind-set, you enjoy working in a team with highly motivated people dedicated to developing the next generation of pharmaceuticals. At the same time, you should work systematically and can adhere to strict documentation and quality standards. You have excellent collaborative skills, agility and flexibility are a natural part of your approach to interact with colleagues in the department and with your stakeholders. Working at Novo Nordisk Novo Nordisk is its people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees. Together, we go further. Together, we’re life changing. Contact For further information, please contact Associate Manager Jens Toft Hummelshøj at +45 3077 5768. Deadline 15th of August 2023 Applications will be reviewed on an ongoing basis. 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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".

    Arbejdsstedet er beliggende i Måløv.

    Jobbet er oprettet på vores service den 3.7.2023, men kan have været deaktiveret og genaktiveret igen.

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    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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