Senior GMP Quality Assurance Lead – Pharma/Biotech

Resourcing Life Science Ltd.; France; On-site; EUR 60,000 - 90,000; Full time

Job summary

Resourcing Life Science Ltd. in France is seeking an experienced Quality Assurance professional to ensure GMP compliance across manufacturing and finished products, review SOPs, and guarantee accurate release documentation.

The ideal candidate holds a bachelor’s or master’s in a scientific field, with at least five years in QA in pharma/biotech and hands-on knowledge of audits, deviations, and CAPA systems to drive continuous improvement and quality culture.

Qualifications

• Bachelor’s or Master’s degree in a scientific or technical field.
• Minimum five years in Quality Assurance in pharma/biotech or GMP-regulated environment.
• Hands-on knowledge of GMP, audits, deviations, and CAPA systems.

Responsibilities

• Maintain GMP compliance across manufacturing processes and finished products.
• Review, develop and update SOPs, work instructions and quality documentation.
• Assess production and batch documentation for accuracy and compliance.
• Investigate quality incidents and deviations; identify root causes and implement CAPAs.
• Manage customer complaints; oversee investigations and coordinate CAPA implementation.
• Plan and perform internal audits; document findings and improvements.
• Coordinate external audits and inspections by customers and regulatory authorities.
• Compile annual product quality reviews and assess quality system performance.
• Support quality discussions with internal teams and external partners; review quality agreements.
• Advise production teams on quality requirements and promote GMP awareness.

Skills

Quality Assurance

GMP familiarity

Audit management

CAPA system

KPI monitoring

Education

Bachelor's or Master's degree in a relevant field

Job description

Resourcing Life Science Ltd. in France is seeking an experienced Quality Assurance professional to ensure GMP compliance across manufacturing and finished products, review SOPs, and guarantee accurate release documentation.

The ideal candidate holds a bachelor’s or master’s in a scientific field, with at least five years in QA in pharma/biotech and hands-on knowledge of audits, deviations, and CAPA systems to drive continuous improvement and quality culture.