Audit Manager GxP (GLP, GCP, GVP)

Responsibilities

• Conduct GCP, GLP, and GVP audits as a lead auditor or team member, covering internal processes, investigator sites, vendors, and service providers
• Coordinate regulatory inspection support activities for agencies such as the FDA, EMA, MHRA, and Health Canada
• Support the risk-based audit programme, including 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 meet regulatory requirements
• Support the development, maintenance, and periodic review of GxP SOPs and QMS documentation
• Act as a quality partner to stakeholders by advising on compliance questions and issue resolution
• Assist with quality metrics and trend analysis to identify compliance risks
• Support investigations into compliance issues, serious breaches, or quality events
• Deliver training and coaching to business functions to promote GxP awareness and a strong quality culture

Requirements

• 6+ years of pharmaceutical industry experience in R&D or Quality/Compliance roles
• Bachelor of Science degree in Chemistry, Pharmacy, Biology, Life Science, Public Health, or Healthcare
• Working knowledge of GCP, GLP, and GVP regulations and guidelines
• Ability to perform audits using a risk-based approach
• Strong stakeholder management, communication, and documentation skills
• Willingness to travel domestically and internationally as required

Preferred Qualifications

• Master of Science or PhD in Biology, Biochemistry, or an equivalent field

About the Company

Haleon is a purpose-driven, world-class consumer company dedicated to putting everyday health in the hands of millions. With a trusted portfolio of brands including Sensodyne, Panadol, Advil, and Centrum, we combine deep human understanding with trusted science to deliver better everyday health with humanity.