Senior Audit Lead – GMP Audits for EMEA Supply Chain

About the role

GSK is seeking an experienced Senior Audit Lead to drive GMP and compliance audits across its EMEA supply‑chain network. You will work within the Quality organisation, supporting senior management by identifying, prioritising and monitoring quality, compliance and technical risks in sterile, biopharm, vaccine and pharmaceutical facilities.

Key responsibilities

• Plan, execute and manage unannounced, for‑cause and targeted GMP audits of internal and external manufacturing sites, R&D centres and logistics service providers.
• Audit Global Supply Chain sites, Local Operating Companies and external partners that supply highly regulated markets.
• Produce clear, concise audit reports and ensure corrective action plans are implemented.
• Engage with senior stakeholders such as Supply Chain Directors, Site Directors, Quality Directors and R&D leaders.
• Provide sterile manufacturing subject‑matter expertise to the EMEA auditing team.

Required profile

• Degree in a scientific, technical or engineering discipline.
• Extensive experience in sterile, biopharm and/or vaccine manufacturing environments.
• Proven track record of conducting GMP and compliance audits.
• Strong communication and influencing skills across senior leadership.

Required skills

• In‑depth knowledge of GMP regulations.
• Expertise in sterile manufacturing processes.
• Familiarity with biopharm and vaccine production technologies.
• Audit planning, execution and reporting.