Quality Assurance - GMP&Clinical (d/f/m)

- Globally operating pharmaceutical company - Temporary assignment for 12-24 months **About Our Client** For our client, a globally renowned pharmaceutical company in the Basel area, we are seeking a Quality Assurance (GMP&Clinical) professional to strengthen the team in 2026 in support of Phase 3 development activities. The contract duration is 12-24 months and is open to candidates with 5+ years of relevant experience across different seniority levels. Depending on the selected candidate's performance and motivation, the possibility of an extension or a permanent take over. **Job Description** Depending on the candidate`s seniority, the incumbent will provide Quality Assurance oversight for Phase 3 clinical development, ensuring GMP and GCP compliance for clinical trial material and trial execution (small molecules drugs). - Lead / Support establishment and maintenance of the Quality Management System appropriate for Phase 3 - Own / Contribute to GMP oversight of drug substance, drug product, packaging, labeling, and testing activities - Manage / Coordinate batch record review, lot disposition, and clinical supply release - Lead / Support deviation, CAPA, and change control activities impacting Phase 3 material - Oversee / Participate in vendor and CDMO quality oversight and audits - Ensure / Support inspection readiness for GMP and GCP inspections - Lead / Support Quality input to stability programs and expiry management - Approve / Review quality documentation depending on delegated authority **The Successful Applicant** **In order to be considered for the role, the selected candidate must have:** - Degree in Life Sciences disciplines - Relevant experience in QA phase 3 (small molecules): - ~5-7 years: Executes QA activities, supports audits/inspections, manages assigned systems - ~8-10 years: Leads QA activities, acts as primary QA contact for Phase 3 program - 10+ years: Owns QA strategy, leads inspections, accountable for quality risk - Strong communication skills in English - Passion for Drug Development (small molecules) **What's on Offer** The selected candidate will be part of a dynamic team in an international environment and actively contribute to shape, develop, and drive the market authorization of innovative drugs. Hybrid work model (3 days onsite). Extension or take-over possibility. **Contact: Kamila Fotiou** **Quote job ref: JN-122025-6909327** Quelle: https://ch.linkedin.com/jobs/view/quality-assurance-gmp-clinical-d-f-m-at-michael-page-4345590785

Level: mid level