Principal Scientist Parenteral Dosage Forms


Reference Number: 895552-W
Type of placement: Contract, 5 months
Location: Switzerland, North West


Our client is a privately held Swiss Specialty Pharma company with focus on the development of drugs that address rare and hard to treat diseases. As they are expanding their clinical development activities, they are currently looking for a

Main Responsibilities:

  • Late phase process development and process transfer to commercial site(s) of parenteral dosage forms
  • GxP documentation preparation (e.g. FMEAs, QTPPs, QRAs, ) for late phase / transfer projects
  • Project management incl. e.g. detailed project schedule planning & progress tracking, resource & budget planning and tracking, project risk analysis and management
  • Coordination of activities and interfaces (e.g. development, analytical, device laboratory activities, interaction between development and commercial site)

Qualifications and Experience:

  • Pharmacist, Pharmaceutical Engineer or other equivalent natural science education
  • Ph.D. in Pharmaceutical Technology or related scientific fields
    3 to 5 years of experience in pharmaceutical industry
  • proven track record of working with parenteral primary packaging (e.g. syringes, vials) materials
  • Swiss work permit or EU-citizenship necessary

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