2 - 6 years
3 - 7 Lacs
Posted:3 weeks ago|
Platform:
Work from Office
Full Time
Coordinate and compile product data from various departments (Production, QC, QA, Warehouse, etc.) for APQR. Review manufacturing, testing, and deviation records to identify trends and areas for improvement. Ensure compliance with regulatory and company requirements for APQR documentation. Analyze critical quality attributes, in-process parameters, and batch performance. Identify corrective and preventive actions (CAPA) based on APQR findings. Prepare and finalize APQR reports within defined timelines. Support audits and regulatory inspections by presenting APQR documentation. Ensure timely closure of action items identified during the APQR process.
AMNEAL PHARMACEUTICALS COMPANY (INDIA) PRIVATE LIMITED
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My Connections AMNEAL PHARMACEUTICALS COMPANY (INDIA) PRIVATE LIMITED
Pharmaceutical Manufacturing
5001-10000 Employees
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