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

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 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.

Equal Opportunities

Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected – all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It's important to us that Haleon is a place where all our employees feel they truly belong.

During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees. The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.