Job Overview
Required Skills
Job Description
Responsible for monitoring manufacturing and packing activities to ensure compliance with approved procedures and GMP requirements.
Key Responsibilities:
• Perform IPQA activities in manufacturing and packing areas.
• Conduct line clearance and area clearance.
• Monitor in-process manufacturing activities.
• Review BMR/BPR and production documentation.
• Ensure compliance with SOPs and GMP.
• Identify deviations and support investigations.
• Assist in CAPA and change-control activities.
• Monitor environmental and hygiene requirements.
• Support internal and external audits.
• Coordinate with Production and QC departments.
• Ensure proper documentation and data integrity.
Experience Requirements:
• 1–5 years relevant pharmaceutical QA/IPQA experience.
• Strong knowledge of GMP and documentation.
• BMR/BPR and SOP knowledge preferred.