Quality Assurance GMP France

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

Your responsibilities

• Maintain compliance with GMP requirements and applicable quality regulations across manufacturing processes and finished products.
• Review, develop and update SOPs, work instructions and quality documentation, ensuring these are followed consistently in daily operations.
• Assess production and batch documentation for accuracy and compliance, taking appropriate action when products do not meet release requirements.
• Investigate quality incidents and deviations, work with relevant departments to identify root causes, and ensure corrective and preventive actions are implemented effectively.
• Manage customer complaints, oversee investigations and coordinate the implementation of appropriate CAPAs.
• Plan and perform internal audits, document findings and ensure agreed improvements are completed.
• Coordinate external audits and inspections by customers and regulatory authorities, including preparation, responses and follow-up activities.
• Compile annual product quality reviews, assess quality system performance and prepare required reports and management information.
• Support quality-related discussions with internal teams and external partners, including the preparation and review of quality agreements.
• Advise production teams on quality requirements, promote GMP awareness and encourage a strong quality culture throughout the organization.
• Identify opportunities to improve Quality Assurance processes, monitor relevant KPIs and contribute to departmental performance reporting.

Your profile

• A bachelor’s or master’s degree in a relevant scientific or technical discipline.
• At least five years of Quality Assurance experience / GMP-regulated environment in pharma / biotech
• Practical knowledge of GMP requirements, audit processes, deviation management and CAPA system