Quality Assurance Specialist – Raw Material
vor 1 Woche
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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