08 Aug
|
BDR Pharmaceuticals
|
Padra
08 Aug
BDR Pharmaceuticals
Padra
Role & responsibilities :
Support technology transfer from R&D; to commercial manufacturing.
Monitor manufacturing processes and identify prospects for process improvement.
Review Batch Manufacturing Records (BMR), Process Flow Diagrams (PFD), SOPs, and process documentation.
Assist in process scale-up, trial batches, exhibit batches, validation batches, and commercial batches.
Participate in Process Validation, Equipment Qualification (IQ/OQ/PQ), and Process Verification activities.
Investigate process-related deviations and support Root Cause Analysis (RCA) and CAPA implementation.
Coordinate with cross-functional teams including Production, QA, QC, Engineering, and Warehouse.
Prepare and maintain process-related documentation, validation reports,
SOPs, and change controls.
Ensure compliance with cGMP, regulatory guidelines, EHS, and Data Integrity requirements.
Support continuous improvement initiatives to enhance productivity, yield, and operational efficiency
Preferred candidate profile
Designation : Officer/Sr. Officer
Location: Vadodara,Luna, Padra Gujarat
Department: Process Engineering
Employment Type: Full time
Industry: Pharmaceuticals, Only API
Experience: 25 Years
Education: B.E./B.Tech (Chemical Engineering)
📌 Officer, Process Engineering Padra
🏢 BDR Pharmaceuticals
📍 Padra