Global GMP Compliance Auditor — Remote, Travel‑Heavy

Lonza; Manchester; A distancia; GBP 90.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Agile career culture

Inclusive workplace

Local benefits tailored to locality

Global benefits access

Descripción de la vacante

Lonza is seeking a Corporate Compliance Auditor based in Manchester with substantial international travel (50–60%). You will design, plan and execute global cGMP audits across biologics, cell and gene therapies, sterile products, APIs and related operations.

In this high-visibility role you will partner with manufacturing sites to elevate standards, navigate regulatory landscapes and ensure inspection readiness; you will mentor auditors and contribute to continuous quality improvements.

Formación

• 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.
• Advise sites on regulatory compliance, risk assessment, remediation strategies, and health authority inspection preparation.
• Mentor junior auditors, provide senior compliance guidance, and drive continuous quality improvement.

Responsabilidades

• Lead global cGMP compliance audits across biologics, cell/gene therapies, sterile products and APIs.
• Advise sites on regulatory compliance and inspection readiness.
• Perform supplier quality assessments and act as SPOC for suppliers.
• Mentor auditors and drive continuous improvement across business units.
• Partner with manufacturing sites to elevate standards and ensure ongoing readiness.

Conocimientos

cGMP QA/auditing

MHRA/HPRA inspections

Regulatory compliance

Audit leadership

Supplier QA/audits

Mentoring auditors

Educación

MSc in Chemistry, Biochemistry, Pharmacy, or related field

Descripción del empleo

Lonza is seeking a Corporate Compliance Auditor based in Manchester with substantial international travel (50–60%). You will design, plan and execute global cGMP audits across biologics, cell and gene therapies, sterile products, APIs and related operations.

In this high-visibility role you will partner with manufacturing sites to elevate standards, navigate regulatory landscapes and ensure inspection readiness; you will mentor auditors and contribute to continuous quality improvements.