CQV Compliance Specialist - Drive Quality & CAPAs

Evotec WD; Toulouse; Sur place; EUR 55 000 - 85 000; Plein temps

Résumé du poste

Evotec in Toulouse is looking for a CQV Compliance Specialist (F/M/D) to support MSAT quality systems and regulatory alignment in a cGMP environment. The role focuses on documentation, deviations, CAPAs, and change controls.

You will partner with MSAT, Quality, and Manufacturing across sites, coordinate document lifecycles, perform investigations with root cause analysis, and drive continuous improvement in compliance processes.

Qualifications

• Bachelor's degree in a scientific, engineering, or technical field.
• 4–5 years of experience in a cGMP-regulated manufacturing environment.
• Fluent in French and English with strong communication.

Responsabilités

• Coordinate quality and compliance documentation for MSAT teams.
• Lead investigations and CAPA follow-up with root cause analysis.
• Manage deviations, change controls, and related action plans.
• Monitor compliance trends and support data-driven decisions.
• Collaborate with Quality, Manufacturing, and MSAT teams.

Connaissances

French (Fluent)

English (Fluent)

Root cause investigations

FMEA

cGMP knowledge

Quality systems

Documentation management

Formation

Bachelor's degree in science/engineering

Description du poste

Evotec in Toulouse is looking for a CQV Compliance Specialist (F/M/D) to support MSAT quality systems and regulatory alignment in a cGMP environment. The role focuses on documentation, deviations, CAPAs, and change controls.

You will partner with MSAT, Quality, and Manufacturing across sites, coordinate document lifecycles, perform investigations with root cause analysis, and drive continuous improvement in compliance processes.