Senior QA Auditor — Compliance & Audit Management

Lonza; Singapore; On-site; Confidential; Full time

Benefits offered by this job

Medical insurance

Family coverage

Transport provided

Career growth

Global exposure

Competitive pay

Job summary

Lonza Singapore is seeking a Lead Specialist, Compliance (Audit Management) to support audit activities for a multi-product, cGxP contract manufacturing facility. This fully site-based role emphasizes close collaboration and precision in manufacturing medicines.

You’ll lead audit prep, responses, deviation investigations, and document ownership, while developing training capabilities and SME-level expertise.

Qualifications

• Bachelor’s degree with relevant QA experience in biopharma or GMP environments.
• Solid understanding of GMP, quality systems and regulatory expectations.
• Experience collaborating with cross-functional manufacturing teams.
• Familiarity with FDA/EMA/ICH guidelines and inspection readiness.

Responsibilities

• Lead in audit walk-down preparation and provide feedback.
• Lead audit/inspection responses and deviation investigations.
• Maintain ownership of quality documents for the assigned processes.
• Develop training materials and act as a SME in assigned domains.
• Support regulatory inspections and customer audits as required.

Skills

QA operations

GMP compliance

Cross-functional collaboration

Regulatory knowledge

Analytical abilities

Communication skills

Organizational skills

Detail-oriented

Education

Bachelor's degree in life sciences / QA

Job description

Lonza Singapore is seeking a Lead Specialist, Compliance (Audit Management) to support audit activities for a multi-product, cGxP contract manufacturing facility. This fully site-based role emphasizes close collaboration and precision in manufacturing medicines.

You’ll lead audit prep, responses, deviation investigations, and document ownership, while developing training capabilities and SME-level expertise.