Global Quality Manager

About the role

We are seeking a qualified Global Quality Manager to lead quality assurance activities for a leading pharmaceutical company. The role is based in Basel and offers up to 40% remote work.

Key responsibilities

• Act as Delegate of the Swiss Responsible Person (FvP) with final quality decision support.
• Provide global QA oversight for the IMP distribution network and PTDS‑L.
• Lead deviation and CAPA oversight, including quality impact assessments and third‑party evaluation reviews.
• Own quality documentation and change control for internal procedures and PTDS‑L business documents.
• Drive inspection and audit readiness and manage temperature excursion assessments for clinical trials.
• Enable clinical studies through 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.

Required profile

• Bachelor’s degree in a scientific or technical field such as Pharmacy, Chemistry, Biology, or Engineering.
• Minimum 3 years of comprehensive Quality Assurance experience with a strong compliance focus.
• Deep knowledge of regulated GxP environments (GMP/GDP), preferably with distribution or supply‑chain exposure.
• Fluent English (written and spoken); German required for critical quality/regulatory documentation and health‑authority inspections.

Required skills

• Veeva Vault QMS

What we offer

• Fixed‑term contract (12 months) with possible extension.
• Hybrid work model with up to 40% home‑office.
• Opportunity to influence global quality strategy in a leading pharma environment.