Global Quality Manager (m/f/d)

Description du poste

For a leading pharmaceutical company, we are looking for a qualified General Information: Location: Basel Workload: 100% Start: 21.08.2026 Duration: 12 months (Extension possible) Home Office: max. 40% Your Responsibilities: Act as Delegate of the Swiss Responsible Person (FvP) with final quality decision support. Provide global QA oversight for the IMP distribution network (depots) and PTDS?L. Lead deviation & CAPA oversight, including quality impact assessments and third-party evaluation review. Own quality documentation & change control (internal procedures + PTDS?L business documents). Drive inspection/audit readiness and manage temperature excursion assessments for clinical trials. Enable clinical studies via flowchart/transfer/expert opinion approvals, quality agreements, and complaint management. Ensure GMP/GDP compliance, adherence to Good Documentation Practices, and training compliance with PQS documents. Your Profile: Bachelor’s degree in a relevant scientific/technical field (e.g., Pharmacy, Chemistry, Biology, Engineering). Minimum 3 years of proven, comprehensive Quality Assurance experience with a strong compliance focus. Deep knowledge of regulated GxP environments (GMP/GDP), ideally with distribution/supply chain exposure. Fluent in English (written and spoken); German is a strong asset—required for authoring critical quality/regulatory documentation and supporting Health Authority Inspections. Nice-to-haves Familiarity with Veeva Vault QMS PTQ experience Experience in supplier management, especially depots Interested? Then apply today. We look forward to hearing from you!