QA CQV Expert
Vor 2 Tagen
We're Hiring: QA CQV Expert (Consultant)
– 14-month contract | Switzerland
Are you an experienced QA professional with a strong background in commissioning, qualification, and validation (CQV) within GMP environments?
We're looking for a
QA CQV Expert
to support a major biotech project involving new manufacturing premises and equipment. This is a
14-month consulting opportunity
starting
November 2025
, based in
Fenil-sur-Corsier, Switzerland
.
Key Responsibilities:
- Act as QA representative for engineering projects
- Review validation deliverables (plans, protocols, URS, risk assessments)
- Oversee qualification of equipment, premises, and clean utilities
- Lead or review deviations and CAPAs
- Collaborate cross-functionally with Engineering, QC, and Manufacturing
Your Profile:
- 5–10 years in GMP biotech/pharma environments
- Degree in Engineering, Biotechnology, Pharmacy, or Quality Management
- Fluent in French; English proficiency a plus
- Strong knowledge of FDA/EMA/ICH regulations and CSV
If you're autonomous, pragmatic, and thrive in dynamic environments, we'd love to hear from you
DM me or apply directly to learn more.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
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