GMP QA Lead – Site-Based Quality & Compliance

Lonza Group Ltd.; Slough; On-site; Confidential; Full time

Benefits offered by this job

Agile work culture

Inclusive workplace

Competitive compensation

Job summary

Lonza seeks an Associate Principal QA Specialist to provide QA review and oversight across studies and activities, ensuring GMP compliance and alignment with Global Quality Standards. You will act as a GMP SME, implementing robust quality processes, supporting operations, and driving continuous improvement within QC and Development Services.

This is a fully site-based role with emphasis on collaboration and quality culture.

Qualifications

• BSc or equivalent experience in a scientific subject preferred.
• Experience developing quality assurance plans for technical operations.
• Experience in quality audits and inspections of technical processes.

Responsibilities

• Provide QA review, approval, and guidance for deviations, CAPAs, change controls, investigations, and OOS records.
• Provide QA oversight for QC, MSAT, and Development Services activities.
• Act as GMP SME, offering strategic quality support to Operations, QC, MSAT, and Development Services.
• Mentor and develop team members in cGMP principles.
• Maintain audit readiness through area walkthroughs and inspections.

Skills

GMP

QA Oversight

QMS

CAPA Mgmt

Deviations Handling

Audits

Quality Systems

Mentoring

Process Improvement

Documentation

Education

BSc or equivalent

Tools

GxP Knowledge

Job description

Lonza seeks an Associate Principal QA Specialist to provide QA review and oversight across studies and activities, ensuring GMP compliance and alignment with Global Quality Standards. You will act as a GMP SME, implementing robust quality processes, supporting operations, and driving continuous improvement within QC and Development Services.

This is a fully site-based role with emphasis on collaboration and quality culture.