Officer, Process Engineering

BDR Pharmaceuticals; Padra; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

BDR Pharmaceuticals seeks an Officer/Sr. Officer in Process Engineering to support technology transfer from R&D to commercial manufacturing in Vadodara, Gujarat. You will monitor processes, review BMRs and PFDs, and assist in scale-up and validation batches.

The role requires deep knowledge of cGMP, QA collaboration, and documentation rigor. You will participate in IQ/OQ/PQ, CAPA, and continuous improvement initiatives to boost productivity and yield.

Qualifications

• 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.

Responsibilities

• Prepare and maintain process-related documentation, validation reports, SOPs, and change controls.
• Support continuous improvement initiatives to enhance productivity, yield, and operational efficiency.

Education

B.E./B.Tech (Chemical Engineering)

Job description

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)