Job Description

Roles & Responsibilities

about the position

Join the Quality department to contribute to the handling of CAPAs and deviations in compliance with GMP standards and regulatory requirements of the pharmaceutical industry. You will participate in the implementation of corrective and preventive actions to ensure compliance and continuous improvement of quality processes.

Location: Casablanca
Duration: Permanent Contract
Experience: 0-3 years in the pharmaceutical industry
Languages: Good level of French and English

Job duties

• Manage and monitor CAPAs (Corrective and Preventive Actions) and deviations in accordance with internal and regulatory procedures.
• Participate in the analysis of root causes and the definition of action plans.
• Ensure documentation and traceability of actions in the quality system.
• Contribute to the continuous improvement of quality processes and GMP compliance.

Your profile

• Diploma m(e) in pharmacy, science or biology (quality, biology, pharmaceutical industry).
• First experience or internship in quality assurance or pharmaceutical production (0-3 years).
• Knowledge of GMP and quality tools (CAPA, deviations) .
• Rigour, organisation and ability to work in a team.

Desired Candidate Profile

Diploma m(e) in pharmacy, science or biology (quality, biology, pharmaceutical industry).

First experience or internship in quality assurance or pharmaceutical production (0-3 years).

Knowledge of GMP and quality tools (CAPA, deviations) .

Rigour, organisation and ability to work in a team.