QC Analyst – Quality Control Laboratory

About the role

Hikma Pharmaceuticals is seeking a motivated QC Analyst to join its Casablanca laboratory. You will work in a supportive environment that values innovation, care, and collaboration, contributing to the production of high‑quality medicines.

Key responsibilities

• Perform stability, validation, raw material, packaging material, semi‑finished and finished product analyses.
• Conduct both manual and automated laboratory tests.
• Calibrate and adjust laboratory equipment.
• Prepare and store reagents according to established procedures.
• Follow the analysis schedule and compare results against current standards.
• Identify anomalies, contribute to their resolution, and record verified results.
• Issue analysis reports and propose improvements in equipment organization.
• Maintain workstations and provide technical training to new team members.

Required profile

• Bachelor’s degree (Bac+3/4) in Chemistry, Pharmaceutical Quality Control/Analysis, or a related field.
• Strong knowledge of GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices).
• High level of accuracy, attention to detail, and strong organizational skills.
• Team spirit with the ability to collaborate across logistics, production, quality assurance, and maintenance.
• Autonomous, proactive mindset.

Required skills

• Proficiency with GMP and GLP standards.
• Familiarity with laboratory equipment and IT systems.
• Ability to write procedures and analytical reports.