Senior Process Development Specialist

Ferring Pharmaceuticals

Kastrup, Denmark
Onsite
Process development and gmp manufacturing expertise
Late-stage drug product development
Gmp and aseptic/sterile drug product manufacturing
Ferring Pharmaceuticals is seeking a Senior Process Development Specialist to lead late-stage drug product development in Kastrup, Denmark. The role involves collaboration across various functions to ensure compliance with regulatory standards and successful project execution in a dynamic, team-oriented environment

Job Summary

  • This role offers broad organizational exposure and collaboration and is a chance to truly stand out in a lean organization where great work is quickly recognized.
  • You will join a small, highly dedicated team supporting projects at late stages of development, working with peptides, small molecules, proteins, gene therapies, and microbiome-based therapies.
  • You will work with process development and IMP manufacturing, focusing on developing a robust manufacturing process which comply with regulatory requirements whilst meeting the expectations of commercial manufacturing.

Matching Summary

Match Score: 85

Ferring Pharmaceuticals is seeking a Senior Process Development Specialist to lead late-stage drug product development in Kastrup, Denmark. The role involves collaboration across various functions to ensure compliance with regulatory standards and successful project execution in a dynamic, team-oriented environment.

Skills & Requirements

Must-have

  • process development and GMP manufacturing expertise
  • late-stage drug product development
  • GMP and aseptic/sterile drug product manufacturing
  • CTD authoring and regulatory documentation
  • technology transfer to commercial manufacturing

Nice-to-have

  • collaborative mindset and cross-functional work
  • structured problem-solving tools
  • interest in project management

Key Requirements

  • Subject matter expert (> 10 years)
  • M.Sc. in pharmaceutical process science
  • Experience in late-stage drug product development
  • Proven experience in CTD authoring
  • Demonstrated scientific project management skills

Work Rights

Must be located in the Øresund region

Tailored Resume

Cover Letter