07 Aug
|
BDR Pharmaceuticals
|
Padra
07 Aug
BDR Pharmaceuticals
Padra
Role & responsibilities :
- Support technology transfer from R&D; to commercial manufacturing.
- Monitor manufacturing processes and identify opportunities 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