Associate Director, Quality Auditor, GVP

Associate Director, Quality Auditor, GVP

Closing Date: 9th October 2026 (COB)

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success.

We're uniting science, technology, and talent to get ahead of disease together.

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Our approach to R&D

We are seeking an experienced and strategic quality professional to join GSK as an Associate Director, Quality Auditor, GVP within R&D Quality and Risk Management.

The purpose of this role is to provide independent Quality Assurance across GSK R&D by delivering comprehensive global audit programmes and influencing quality and compliance strategies. This position plays a key leadership role in ensuring compliance with international pharmacovigilance regulations, GSK policies and procedures, and industry best practices. The successful candidate will define audit scope and methodology, lead complex audits, identify emerging compliance trends, drive quality improvements across the organisation, and support regulatory inspections.

This is an influential position requiring strong leadership, expert knowledge of pharmacovigilance quality systems, and the ability to partner effectively across multiple functions and geographic regions.

• Lead and deliver risk-based pharmacovigilance audits across processes, systems and third parties to assess compliance with global regulatory requirements and GSK standards.
• Develop and execute audit strategies and plans that align with organisational priorities and emerging compliance risks.
• Provide independent quality oversight by identifying compliance risks, evaluating quality systems, and recommending sustainable improvements.
• Lead discussions with senior stakeholders to communicate audit outcomes, drive effective corrective and preventive actions (CAPAs), and monitor their implementation and effectiveness.
• Analyse audit data, compliance trends, and quality metrics to identify systemic issues and opportunities for continuous improvement.
• Serve as a key quality partner during regulatory inspections and inspection readiness activities.
• Provide expert advice on pharmacovigilance regulatory expectations, quality risk management, and compliance practices.
• Influence and collaborate across global matrix teams to strengthen quality culture and compliance performance.
• Coach, mentor and develop auditors and business partners, sharing best practices and contributing to organisational capability building.

• Bachelor's degree or equivalent in a scientific, pharmacy, life sciences, quality-related discipline, or equivalent combination of education, training and experience.
• Significant experience within the pharmaceutical industry, quality assurance and/or pharmacovigilance.
• Extensive knowledge of global pharmacovigilance regulations and quality management expectations.
• Demonstrated experience planning and leading complex quality audits.
• Experience developing corrective and preventive action strategies and evaluating effectiveness.
• Strong analytical, organisational, and planning skills.
• Proven ability to work effectively across global matrix organisations.
• Excellent verbal, written and presentation skills.
• Ability and willingness to travel domestically and internationally…