Compliance Auditor x3

Overview

Lead global corporate cGMP compliance audits and provide regulatory, quality, and remediation guidance across manufacturing sites and operational facilities.

What you'll do

• Plan and execute global corporate cGMP compliance audits.
• Advise sites on remediation actions and regulatory inspection preparation.
• Provide GMP compliance expertise and best-practice guidance.
• Perform supplier quality assessments and audits.
• Act as the single point of contact for assigned suppliers.
• Monitor compliance risks across business units.
• Mentor and coach auditors.

What you'll need

• 10+ years of cGMP quality assurance or auditing experience.
• Previous experience as an MHRA or HPRA Health Authority Inspector.
• Experience carrying out cGMP inspections.
• Experience auditing biologics, cell and gene therapies, sterile products, or APIs.
• An MSc or equivalent in Chemistry, Biochemistry, Pharmacy, or a related field.
• Experience with regulatory compliance, risk assessment, and remediation strategies.

Details

• Location: Manchester, United Kingdom.
• Remote role.
• International travel: 50–60%.