Global Quality Manager

About the role

We are seeking an experienced Global Quality Manager to lead quality, integrity and regulatory compliance of Investigational Medicinal Products (IMPs) across our worldwide clinical supply chain. Based in Basel, the role offers extensive exposure to GxP processes, international stakeholders and continuous improvement initiatives.

Key responsibilities

• Act as delegate of the Swiss Responsible Person (FvP) with final quality decision authority.
• Ensure GMP/GDP compliance for all IMP activities and manage product quality impact assessments.
• Lead deviation management, CAPA assessment and approval.
• Maintain global QA oversight of the IMP distribution network and key supply‑chain partners.
• Review third‑party quality evaluations, master quality agreements and quality agreements.
• Oversee the full lifecycle of quality documentation, change controls and internal/external procedures.
• Drive GxP inspections, audits and health‑authority interactions.
• Manage temperature excursions, complaint handling and IMP supply & release flowcharts.
• Collaborate with external partners and depots to ensure network compliance and support cross‑functional improvement projects.

Required profile

• Bachelor’s degree in Pharmacy, Chemistry, Biology, Engineering or a related scientific/technical field.
• Minimum 3 years of Quality Assurance experience in a regulated GMP/GDP environment.
• Strong knowledge of quality systems, regulatory compliance and inspection readiness.
• Excellent written and spoken English; German is a strong asset.
• Proven ability to manage complex documentation and provide clear regulatory guidance.
• Analytical thinking and problem‑solving skills, with experience in international, cross‑functional teams.

Required skills

• Experience with electronic Quality Management Systems such as Veeva Vault QMS.