Quality Assurance Analyst – Pharmaceutical Manufacturing

About the role

Hikma is seeking a motivated Quality Assurance Analyst to join its pharmaceutical manufacturing site in Portugal. The role involves ensuring that injectable medicines are produced in compliance with strict regulatory standards and internal quality procedures.

Key responsibilities

• Conduct and verify analysis of bulk samples and in‑process controls during batch filling.
• Perform post‑cleaning verification of machine parts to confirm cleanliness.
• Coordinate sampling of finished products for Microbiology and Quality Control testing.
• Carry out round checks, inspections, and start‑up activities in production, packaging, and infrastructure areas.
• Execute aseptic practices, cleaning/disinfection monitoring, and visual inspections for defects.
• Approve maintenance requisitions for product release and verify equipment print‑outs.
• Train new QA analysts and support continuous improvement initiatives.

Required profile

• Academic degree in a scientific discipline.
• Ability to multitask, meet tight deadlines and work under pressure.
• Assertive, flexible, detail‑oriented with good English communication skills.
• Good computer proficiency.
• Knowledge of injectable pharmaceutical processes, cGMP, FDA and other regulatory requirements.
• Availability for 8‑hour shifts and own vehicle for site access.

Required skills

• cGMP compliance
• FDA regulatory knowledge
• Injectable pharmaceutical manufacturing expertise

What we offer

• Direct permanent contract with Hikma.
• Competitive salary aligned with the role.
• Life insurance and health insurance extended to student children up to age 24.
• Annual performance bonus.
• Clear growth and development opportunities.