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QA Specialist (m/f)

  • You hold a relevant academic degree as a Biochemist, Microbiologist, Pharmacist or similar
  • You have a minimum of 3 years of experience from a pharmaceutical/biotech organisation and has been working preferably within QC alternatively within QA or production
  • You have experience with and knowledge of GMP and/or interest within the areas of aseptic processing and Environmental Monitoring within API and finished product production
  • You have experience with validation of QC methods and stability
  • Be a part of the process of defining new methods in relation to our expanding pipeline
  • Provide quality support to and build up ongoing QA oversight of the QC and the Production departments
  • Review and approve protocols and reports from the QC area and Production departments
  • Handling of documentation from the Production specifically from the Environmental Monitoring department
  • Review and approval of stability protocols and reports
  • Review and approve SOPs, Process Simulations, Change Requests, OOSs, Deviations and CAPAs
  • Take active part in QA activities for Bavarian Nordic projects

» Job description

Bavarian Nordic
Kvistgaard [DK]

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