Quality Assurance Analyst – Pharmaceutical Production

About the role

The role focuses on ensuring product quality and compliance throughout the pharmaceutical manufacturing process. You will work closely with supervisors and managers to identify quality concerns, implement improvements, and maintain rigorous standards.

Key responsibilities

• Report quality concerns and suggestions for improvement to supervisors/managers.
• Complete assigned trainings in the QA‑In Process Quality Assurance group using the L2LMS (SABA) platform.
• Perform in‑process and finished‑product sampling, including bulk and packed samples.
• Execute hold‑time studies and sample at hold‑time stages for both bulk and packed products.
• Conduct QA rounds to document deviations from SOPs and record observations.
• Maintain and calibrate instruments used in IPQC.
• Review logbooks, environmental monitoring files, and online records such as equipment usage, cleaning, and balance calibration.
• Manage line clearances for various production activities.
• Execute, review, and release/approve documents (BRRs, ESPs) in the PAS‑X system.
• Review and approve batch manufacturing and packing records.
• Participate in equipment qualifications, cleaning validation, and equipment qualification activities.

Required profile

• 1 to 5 years of relevant experience in pharmaceutical quality assurance.
• Graduation in Pharmacy.

Required skills

• PAS‑X System
• SABA L2LMS platform
• Instrument calibration
• Sampling and testing techniques
• Hold‑time study execution
• Equipment qualification
• Cleaning validation