QA Operations Specialist
On-site · Plan-les-Ouates, Geneva, Switzerland
Job Summary
Quality Assurance Operations Specialist to support QA Operations at the Geneva Manufacturing Site, ensuring GMP compliance, leading deviations and CAPA, audits, and collaboration across sterile production, maintenance, packaging, and labs; responsibilities include batch record reviews, release of incoming materials, QA documentation review/issuance, CAPA, change controls, risk analyses, self-inspections, external audits support, training in classified areas, and effective cross-functional communication; requires university degree in Pharmacy/ Chemistry/ Biochemistry and 5+ years in pharmaceutical quality management; French and English fluency.
Required Qualifications
- University degree in Pharmacy, Chemistry or Biochemistry
- Over 5 years in Quality Management in Pharmaceutical Industry
- Solid knowledge of cGMP, including Annex 1
- Experience in lyophilized products and aseptic process
- Indirect Management in project or investigation
- Fluency in French and English (both oral and written)
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