Location
saint georges
Posted
June 04, 2026
Commute
Local Area
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This job is in your area. Enjoy a short commute and work close to home.
Job Description
Elevate quality assurance as an Audit Manager at Haleon, leading GxP audits across GLP, GCP, and GVP. Ensure regulatory compliance while enhancing quality improvement initiatives.
This position requires 6+ years in R&D and Quality/Compliance, focusing on auditing internal processes and vendor practices. You'll lead GxP audits, support regulatory inspections, and manage CAPA follow-ups. The role holds substantial influence over quality culture and requires expertise in GCP, GLP, and GVP standards.
Key Responsibilities:
• Lead GxP audits for assigned processes and sites
• Coordinate support for regulatory inspections, including FDA and EMA
• Document audit observations and assess CAPA responses
• Maintain and develop GxP SOPs and quality metrics
• Provide guidance on compliance and quality improvement
Requirements:
• 6+ years in pharmaceutical R&D and compliance
• Bachelor’s degree in Chemistry, Pharmacy, or Life Sciences
• Master’s degree or PhD is a plu...
This position requires 6+ years in R&D and Quality/Compliance, focusing on auditing internal processes and vendor practices. You'll lead GxP audits, support regulatory inspections, and manage CAPA follow-ups. The role holds substantial influence over quality culture and requires expertise in GCP, GLP, and GVP standards.
Key Responsibilities:
• Lead GxP audits for assigned processes and sites
• Coordinate support for regulatory inspections, including FDA and EMA
• Document audit observations and assess CAPA responses
• Maintain and develop GxP SOPs and quality metrics
• Provide guidance on compliance and quality improvement
Requirements:
• 6+ years in pharmaceutical R&D and compliance
• Bachelor’s degree in Chemistry, Pharmacy, or Life Sciences
• Master’s degree or PhD is a plu...