Drug Product Process Scientist

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Gentofte

Do you want to be part of a dynamic department that holds the responsibility of ensuring well-functioning marketed products and of bringing new products to markets within disease areas of haemophilia and growth disorders? Would you like to bridge products and processes and combine science with business needs? Then you might be the passionate scientist specializing in Drug Product Process we are looking for. The position As Process Scientist in our team, you will be involved in many different activities in relation to process characterization and validation for both new products and marketed products. Examples of activities are:
  • Manufacturing Process Design activities (such as process characterization studies).
  • Test activities for introduction of new development products from CMC (Chemistry, Manufacturing, and Control) Development.
  • Process validation for new products.
  • Technology transfer activities for marketed drug product.
    • Also, you will support the team of regulatory writers when we write the regulatory documentation related to the products. All of this is conducted in cooperation with colleagues in our manufacturing facilities in Denmark. Qualifications To succeed in this role, we expect you to have:
  • An academic degree in science within Engineering, Chemistry, Pharmacy, or similar.
  • +3 years of experience within the field of CMC or manufacturing, e.g. process or product support, transfer or process validation.
  • Knowledge of GMP regulations is an advantage, preferably from the pharmaceutical industry.
  • Fluency in both oral and written English and preferably you can also communicate in Danish.
    • On a professional level, you are open-minded, engaged, curious and able to inspire and motivate your colleagues. You enjoy finding new and smarter ways of thriving in a dynamic environment, always seizing an opportunity for personal and professional development.  As a team player, strong communication and collaboration skills are of key importance to ensure efficiency, as well as a high level of flexibility and adaptability in the context of a changing environment. The role offers good development opportunities e.g. potential for trying out project management skills, covering internal coordination and collaboration within the department About the department Manufacturing Development is a part of Biotech & Rare Disease (BRD) with a team of over 650 colleagues working together to optimize 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 BRD, Novo Nordisk Biotech & Rare Disease (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 For further information, please call, Senior Manager, Sussie Steen Jensen +45 3075 9955 Deadline 12 February 2024. Applications will be screened 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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    Arbejdsstedet er beliggende i Gentofte.

    Jobbet er oprettet på vores service den 21.12.2023, men kan have været deaktiveret og genaktiveret igen.

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