Audit senior lead (emea gmp audit) (parma)

Experteer OverviewIn this Audit Senior Lead role within GSK’s Quality organization, you will lead GMP and Compliance audits of Biopharm, Vaccines and Pharmaceutical facilities across the Global Supply Chain.

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You’ll assess adherence to GMP, policies and regulatory commitments, covering internal and external sites, LOCs, R&D; and LSPs, and provide sterile manufacturing SME input to the EMEA auditing team.

The role emphasizes clear reporting of risks and action plans to senior management, with significant cross-site interaction.

A key hook is contributing to quality and regulatory excellence across a global network while enabling continuous improvement.Retribuzione / BenefitsManage complex stakeholder engagement across the audit network (Site Directors, Site Quality Directors, VPs/Heads of support functions, and R&D; Quality)Audit Global Supply Chain sites, LOCs, external manufacturers, R&D; sites, LSPs, and facilities serving EMEA and other regulated marketsConduct unannounced audits and for-cause audits based on regulatory actions or identified risksPerform process, quality system-specific, and targeted auditsAudit against risk mitigation plans or regulatory citation commitmentsProduce clear, concise audit reports for senior management and ensure corrective actions xlwpduy are implementedResponsabilitàDegree in a relevant Scientific, Technical or Engineering disciplineRelevant and specific experience in Steriles/Biopharm/Vaccines/Pharmaceutical industriesSubject matter expertise in worldwide cGMPs, regulatory requirements, and Quality Management Systems for sterile/pharma manufacturing and packingExperience identifying and managing complex Quality and Compliance risks and issues