QA Associate – GMP Pharmaceutical Manufacturing
Company: Meet Life Sciences Agency
- Location: Zurich, Switzerland
- Seniority: Mid level
- Employment type: Contract
- Posted: 12 days ago
- Offer language: English
Job description
Meet Life Sciences is looking to connect with experienced QA Officers and QA Associates interested in potential upcoming opportunities within the Swiss pharmaceutical and biotechnology sectors.
We are particularly interested in candidates with direct, hands-on experience supporting GMP-regulated manufacturing operations.
Location: Switzerland
Opportunities: Contract assignments
Industry: Pharmaceutical / Biotechnology
Experience: 2–5+ years in GMP Quality Assurance
Relevant Responsibilities
- Reviewing batch manufacturing records and GMP documentation
- Supporting deviations, CAPA investigations and change controls
- Maintaining GMP compliance across manufacturing activities
- Supporting document control, SOP updates and quality systems
- Assisting with internal audits and regulatory inspection preparation
- Working closely with production, QC and quality teams
Candidate Requirements
- At least 2 years' experience in a GMP-regulated pharmaceutical or biotechnology environment
- Previous experience in an operational Quality Assurance role
- Understanding of EU GMP requirements
- Practical experience with deviations, CAPAs, batch documentation or change control
- Based in Switzerland or eligible and able to work on site
- German language skills preferred for German-speaking sites
Please note: This advertisement is for candidate networking and potential upcoming opportunities rather than a confirmed live vacancy.
If you're currently working in GMP Quality Assurance and would be interested in hearing about future opportunities, please apply with your CV, location and availability.
Right to Work: Candidates must already have the legal right to work in at least one of the DACH countries (Germany, Austria or Switzerland). Applicants who do not meet this requirement will not be considered.
