Technical Expert in Pharmaceutical Manufacturing

2 days ago


Copenhagen, Copenhagen, Denmark Novo Nordisk AS Full time
Key Responsibilities

This position involves providing scientific and technical support for downstream purification processes, including process transfer and batch execution at CMOs. The ideal candidate will have extensive experience in downstream purification of peptide-/protein-based therapeutics and a strong understanding of GMP requirements.

About the Team

You will be working with a highly motivated and experienced team, dedicated to driving innovation and ensuring manufacturing success in downstream purification of synthetic peptides.

Required Skills
  • Masters' degree or Ph.D. within chemical or biochemical sciences, chemical engineering, or equivalent.
  • Extensive experience with downstream purification of peptide-/protein-based therapeutics in commercial phase and/or late development phase drug substance manufacturing.
  • High level of relevant GMP experience and understanding of GMP requirements for drug substance manufacturing.
  • Experience with scale-up and process transfer to large-scale manufacturing is required.


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