Quality Assurance (QA) Specialist

About the role

The Quality Assurance Specialist ensures that all pharmaceutical manufacturing processes, materials, and documentation meet GMP, GDP, and internal quality standards. You will support production operations, review batch records, perform sampling, and take part in investigations while maintaining compliance with the Quality Management System.

Key responsibilities

• Oversee manufacturing activities to guarantee GMP compliance and prevent cross‑contamination.
• Conduct in‑process checks, daily floor rounds, and inspect equipment for cleanliness and readiness.
• Inspect and sample received bulk products, collect medicinal and retention samples, and manage quarantine, rejected, and returned materials.
• Review batch records for completeness, ensure proper documentation practices (GDP), and manage pharmaceutical waste according to SOPs.
• Support quality investigations, deviation assessments, and participate in QMS activities such as CAPA, change control, complaints, and product recall documentation.

Required profile

• Bachelor’s degree in science, pharmacy, or a related field.
• 2–5+ years of Quality Assurance experience in the pharmaceutical industry.
• Strong knowledge of GMP and GDP regulatory requirements.
• Good English communication skills (reading, writing, speaking).

Required skills

• Quality Management System (QMS) handling, including change control, deviation, CAPA, complaint, and recall processes.
• Manufacturing oversight and in‑process inspection.
• Batch record review and documentation compliance.
• Sampling and material control procedures.