Global Quality Manager; m​/f​/d

Global Quality Manager (m/f/d) General Information

• Location:
  
  Basel
• Workload:100%
• Start:
  21.08.2026
• Duration:12 months (Extension possible)
• Home Office:max. 40%

• Act as Delegate of the Swiss Responsible Person (FvP) with final quality decision support.
• Provideglobal QA oversight for theIMP distribution network (depots) and PTDS?
  
  L.
• Leaddeviation & CAPA oversight, including quality impact assessments and third-party evaluation review.
• Ownquality documentation & change control(internal procedures + PTDS?L business documents).
• Driveinspection/audit readiness and managetemperature excursion assessments for clinical trials.
• Enable clinical studies viaflowchart/transfer/expert opinion approvals,quality agreements, andcomplaint management.
• EnsureGMP/GDP compliance, adherence toGood Documentation Practices, and training compliance with PQS documents.

• Bachelor’s degreein a relevant scientific/technical field (e.g., Pharmacy, Chemistry, Biology, Engineering).
• Minimum 3 yearsof 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.

• Familiarity with Veeva Vault QMS
• PTQexperience
• Experience in supplier management, especiallydepots