Chargé(e) Assurance Qualité - CAPA & Déviations
Capgemini Engineering · Casablanca
Job description
About the role
Join the Quality department of a global engineering leader to manage CAPA (Corrective and Preventive Actions) and deviations in a GMP‑compliant pharmaceutical environment. You will support the implementation of corrective measures and drive continuous improvement of quality processes.
Key responsibilities
- Manage and track CAPA and deviation cases according to internal procedures and regulatory requirements.
- Participate in root‑cause analysis and define action plans.
- Document and ensure traceability of all actions within the quality management system.
- Contribute to ongoing GMP compliance and continuous improvement initiatives.
Required profile
- Degree in pharmacy, life sciences or biology (quality, biologie, pharmaceutical industry).
- 0‑3 years of experience or internship in pharmaceutical quality assurance or production.
- Knowledge of GMP regulations and quality tools such as CAPA and deviation handling.
- Strong organization, rigor and ability to work in a team.
Required skills
- CAPA management
- Root‑cause analysis
- GMP compliance
- Quality documentation and traceability
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Published 4 hours ago
Expires 1 month from now
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Capgemini Engineering
Casablanca
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