1. Overall Quality Assurance
• Support day-to-day QA operations across Production, Quality Control, Warehouse, Packing and other departments.
• Ensure compliance with cGMP, SOPs and applicable regulatory requirements.
• Coordinate with departments to ensure adherence to established quality systems.
• Assist in identifying and resolving quality-related issues. 2. Documentation & Quality Management Systems
• Review and maintain BMRs, BPRs, SOPs, logbooks and other GMP documentation.
• Assist in handling deviations, change controls, CAPA and other QMS activities.
• Support document control, issuance, review and archival activities.
• Assist in internal audits, regulatory inspections and compliance follow-ups. 3. In-Process Quality Assurance (IPQA)
• Perform IPQA activities in manufacturing and packing areas as required.
• Conduct line clearance, in-process checks and verification of manufacturing activities.




• Monitor compliance with approved manufacturing procedures and documentation practices.
• Coordinate with Production and QC teams on in-process quality requirements. 4. Cross-Functional Coordination
• Work with Production, QC, Stores, Packing and other departments on quality matters.
• Follow up on pending QA observations, documentation and compliance requirements.
• Assist with routine monitoring, reporting and continuous improvement initiatives.
• Undertake additional QA responsibilities assigned by the department head. Qualification & Experience
• B.
Pharm / M.
Pharm / B.
Sc. / M.
Sc. in a relevant discipline.
• 2–5 years of Quality Assurance experience in pharmaceutical manufacturing.
• Working knowledge of GMP, pharmaceutical documentation and quality management systems.
• Exposure to manufacturing, packing and IPQA activities preferred.

📌 Quality Assurance Executive (Indore)
🏢 KAAPRO
📍 Indore