Audit Manager GxP (GLP, GCP, GVP) in Weybridge

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.

POSITION PURPOSE

To support the execution of GxP audit and inspection activities across GCP, GLP, and GVP, ensuring compliance with applicable global regulations and internal quality standards, while contributing to inspection readiness and continuous quality improvement initiatives.

ACCOUNTABILITIES/RESPONSIBILITIES

• Support and conduct GCP, GLP, and GVP audits as a lead auditor for assigned audits or as a team member, including internal processes, investigator sites, vendors, and service providers.
• Contribute to/coordinate regulatory inspection support activities (e.g., FDA, EMA, MHRA, Health Canada), including preparation, coordination, and follow-up actions.
• Support the risk-based audit programme, including audit preparation, execution, reporting, and CAPA follow-up and tracking.
• Document audit observations, assess responses, and review CAPA evidence for adequacy and timely closure.
• Provide quality and compliance support to ensure clinical, non-clinical, and pharmacovigilance activities are conducted in accordance with GCP, GLP, and GVP requirements.
• Support the development, maintenance, and periodic review of GxP SOPs, written standards, and QMS documentation.
• Act as a quality partner to assigned stakeholders by advising on compliance questions, issue resolution, and quality improvement actions.
• Assist with quality metrics, trend analysis, and reporting to support identification of compliance risks and areas for improvement.
• Support investigations of compliance issues, serious breaches, or quality events, escalating issues as appropriate.
• Deliver training and coaching to business functions to promote GxP awareness and a strong quality culture.

QUALIFICATIONS

• 6+ years of pharmaceutical industry experience in R&D and Quality/Compliance roles.
• Bachelor of Science Degree (Minimum Level of Education Required), Specialization in Chemistry, Pharmacy, Biology or Life Science, Public Health or Healthcare Provider.
• Master of Science Degree or PhD Biology, Biochemistry, or equivalent is a preferred Level of Education but not mandatory.

COMPETENCIES AND SKILLS

• Working knowledge of GCP, GLP, and GVP regulations and guidelines.
• Ability to support and perform audits using a risk-based approach.
• Good stakeholder management and communication skills.
• Ability to work independently on assigned tasks with appropriate supervision.
• Strong written, verbal, and documentation skills.
• Organized, detail-oriented, and able to manage multiple priorities.
• Willingness to travel domestically and internationally as required.