Role & responsibilities
- Maintains and documents proper records / log book / BPCRs / Reports as per GDP
- Handling of Chromatography, sterilization & Filtration techniques.
- Coordination with other department VIZ. engineering, QA, QC and R&D for smoothly execution of Technical Documents.
- Coordination with QA for timely issuance, completion, filling of BPCR and other GMP documents.
- Preparation of Performance Verification and PQ and commissioning protocol Understanding & execution of work in line with cGMP.
- Preparation of SOP, BPCR and other Technical Documents.
- Handling of QMS Documents, Handling of DMS.
- Execution of Training related activities of DSP area.
- To ensure the timely dispensing of raw material and Handling of SAP.
- To support in qualification activities of DSP area.
- Execution of Process validation batches. Filling of all records,
- Change Controls and QMS related Documents associated with DSP area.
- Execution of IQ, OQ, PQ of equipments of downstream area.
- Ensuring complete in-process quality control and continuous improvement in process capabilities. Investigating the OOS.OOT and handling process validation& cleaning validation. Plan and actively oversee team and shift activities to meet the production requirements
Job Type: Full-time
Pay: ₹129,036.15 - ₹758,468.42 per year
Benefits:
- Flexible schedule
- Food provided
- Internet reimbursement
- Leave encashment
- Paid sick time
- Provident Fund
Experience:
- total work: 1 year (Preferred)
Work Location: In person
