GMP Specialist Lead

vor 1 Tag


Visp, Schweiz BioTalent Ltd Vollzeit

We are seeking a GMP Specialist Lead to oversee the implementation of quality systems and ensure compliance with regulatory requirements. This includes adhering to ISO/cGMP standards, PIC/S GMP (part 1-2) or EU Guidelines (Annex 1).

The successful candidate will have 5-10 years of QA experience in commercial drug substance/product or aseptic processing, strong knowledge of GMP (inc. Part 11), and aseptic regulations.

Main Responsibilities:

  • Ensure compliance with regulatory requirements
  • Oversight of on-the-floor QA support
  • Independent quality decisions


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