Quality Assurance Officer – CAPA & Deviations
Capgemini Engineering · Casablanca
Description du poste
About the role
Join the Quality department of a leading engineering services firm to manage CAPA and deviation processes in compliance with GMP standards for the pharmaceutical industry. You will support corrective and preventive actions to ensure continuous improvement and regulatory conformity.
Key responsibilities
- Manage and track CAPA (Corrective and Preventive Actions) and deviations according to internal procedures and regulatory requirements.
- Participate in root‑cause analysis and define action plans.
- Document and maintain traceability of all actions within the quality management system.
- Contribute to ongoing improvement of quality processes and GMP compliance.
Required profile
- Degree in pharmacy, life sciences, biology or related field.
- 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
- Deviation handling
- GMP knowledge
- Documentation and traceability in quality systems
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Capgemini Engineering
Casablanca
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