Quality Assurance Analyst (Manufacturing)

About the role

We are looking for a Quality Assurance Analyst to join our QA department at Hikma’s manufacturing site. The analyst will support the production of injectable medicines by ensuring compliance with cGMP, FDA and internal standards through sampling, testing and documentation.

Key responsibilities

• Conduct and verify analysis of bulk samples and in‑process controls during batch filling.
• Perform post‑cleaning verification of equipment and parts to confirm cleanliness.
• Enter and review data in LIMS, logbooks and other records daily, ensuring accuracy.
• Monitor equipment validity, sample finished products for microbiology and QC testing, and carry out aseptic practice checks.
• Perform round checks, visual inspections and acceptance procedures across production, packaging and infrastructure areas.
• Approve maintenance requisitions, support start‑up activities and train new QA analysts.

Required profile

• High school diploma or academic degree in a scientific field.
• Ability to multitask, meet tight deadlines and work under pressure.
• Attention to detail, assertiveness and flexibility.
• Fluency in English and good computer proficiency.
• Knowledge of injectable pharmaceutical manufacturing, cGMP, FDA and other regulatory requirements.
• Willingness to work 12‑hour rotating shifts.

Required skills

• LIMS (Laboratory Information Management System) usage.

What we offer

• Competitive salary aligned with the role.
• Real growth opportunities within a global pharmaceutical company.