Quality Assurance Specialist – Raw Material

vor 1 Woche


Lausanne, Schweiz AXEPTA SA Vollzeit

Main Responsibilities:

  • Collect, review, and complete all documentation required for raw material batch review and disposition.
  • Provide quality oversight for all quality events (e.g., deviations, investigations, CAPA, change control) within the area of responsibility.
  • Act in compliance with legal and regulatory requirements as well as company guidelines.

Your Profile:

  • At least 2 years of experience in realising of raw material in the pharmaceutical industry.
  • Strong knowledge of cGMP, cGDP, and global regulatory requirements related to pharmaceutical manufacturing and testing.
  • Fluency in French and English is mandatory.

Interested? We invite you to submit your application confidentially.



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