Job description

Company culture :

Sothema operates within a performance-driven and competitive culture, where ambition, results orientation and customer focus are key priorities. This dynamic is closely balanced by a collaborative environment that promotes trust, teamwork and close leadership. The company also relies on a structured organization to ensure efficiency, quality and process consistency. An innovation component further complements this balance, supporting adaptability and continuous improvement.

Raw Material Quality Control Manager

Join a dynamic company operating in the pharmaceutical industry as a Raw Material Quality Control Manager. Based in Bouskoura, your main mission will be to ensure the compliance and quality of raw materials used in our production processes.
Missions principales :

• Plan and communicate the analysis schedule within the defined deadlines
• Control the preparation of reagents and solutions needed for analyses, as well as their traceability
• Ensure the calibration and proper functioning of laboratory equipment
• Supervise the execution of physico-chemical and microbiological analyses of raw materials
• Ensure the availability of laboratory needs: glassware, chemicals, consumables, etc.
• Control storage conditions for reagents, reference standards, and consumables
• Manage the raw material sample archive and ensure compliance with retention deadlines
• Develop and update procedures related to laboratory activities
• Identify and propose areas for improvement in work methods and processes
• Develop the team's professional expertise by ensuring technical and regulatory monitoring
• Participate in continuous improvement projects related to laboratory activities
• Monitor team and activity performance through tracking indicators

Profile sought :

• Master's degree (Bac+5), Engineer or Master's in Quality Control, Chemistry, Biology, or equivalent
• Proven experience in the pharmaceutical industry and in team management
• Mastery of quality control protocols and rules
• Good knowledge of raw material and pharmaceutical product statuses
• Knowledge of pharmaceutical standards: GLP, GMP, GCP, GDP, USP, European Pharmacopoeia, etc.
• Team spirit, commitment, rigor, and continuous improvement orientation

To excel in this role, a Master's degree (Bac +5) or higher is required, ideally in the fields of Production, Quality, Safety, or Maintenance. A solid understanding of regulatory requirements and good manufacturing practices in the pharmaceutical sector is essential.

We are looking for someone with significant experience of 5 to 10 years in a similar position, ideally gained within the pharmaceutical industry or a related sector requiring strict quality control. Your professional background should demonstrate mastery of control techniques and proven team management skills.

• Excellent knowledge of raw material analysis and control techniques.
• Mastery of quality standards (GMP, ISO, etc.) and pharmaceutical sector regulatory requirements.
• Proven ability in project management and problem-solving.
• Team management and employee development skills.
• Very good organizational skills, rigor, and reliability.
• Good interpersonal skills and excellent communication abilities, both written and oral.
• Proficiency in computer tools and quality management software.
• Analytical skills and proactivity in suggesting improvements.

If you see yourself in this profile and wish to take on a new exciting challenge within a growing company, we invite you to apply without delay using the button below "Send my CV to the recruiter".