Compliance Auditor x2

Location: Manchester - Remote This role involves significant international travel (50–60%) across global manufacturing sites and operational facilities.

As a Corporate Compliance Auditor, you will play a pivotal role in safeguarding Lonza ’s license to operate by driving compliance excellence and mitigating quality risks worldwide.

Acting as a trusted technical advisor, you will design, plan, and execute high-impact corporate cGMP audits across a diverse global footprint—spanning biologics, cell and gene therapies, sterile drug products, APIs, medical devices, and hardware/software operations.

In this high-visibility global role, you will partner directly with manufacturing sites to elevate standards, navigate complex regulatory landscapes, and ensure continuous inspection readiness.

What you will get: An agile career and dynamic working culture An inclusive and ethical workplace A variety of benefits tailored to your localality.

Access to global benefits via What you will do: Champion Global Excellence: Support the global vision and strategic objectives for HR processes and technology, ensuring alignment with Lonza ’s goals.

Advise and support sites in developing and executing remediation actions, preparing for and managing regulatory inspections, and ensuring compliance. Provide GMP compliance expertise and best practice guidance. Perform Supplier Quality assessments and audits. Act as SPOC for assigned suppliers within a global portfolio.

Monitor and assess compliance risks across business units. Mentor and coach auditors What we are looking for: Mandatory previous experience as a Health Authority Inspector with the MHRA or HPRA (Ireland) carrying out cGMP inspections.

Lead, plan, and execute global corporate cGMP compliance audits across diverse sites, including biologics, cell/gene therapies, sterile products, and APIs. Advise sites on regulatory compliance, risk assessment, remediation strategies, and health authority inspection preparation. Perform supplier a