o Preparation of quality-related documents(viz.SOPs,Validation Protocols and reports, Qualification Protocols and Reports, System procedures, Master production records, specification, etc.) o Calibration of IPQA equipment o Perform qualityin-processchecks o Preparation and review documents of product changeover and cleaning validation procedure. o Line clearance in dispensing & manufacturing department. o Preparing Annual product quality reviews. o Issuance of controlled copies, Logbooks,SOPs,Formats,specifications and records to various departments. o Review Batch manufacturing records, testing protocol,formats,etc. o Handling QMS(Deviation,change Control,Marketcomplaint,etc.)on GMP production area. o Making sure that internal audits (self-inspection)are performed. o To ensure Q.A.activities are carried out as per set procedures and ensure to record in respective documents. • Review of BMR & BPR. o Compilation of Planned/unplanned Deviation & Change Control Documents System. o To follow the EHS Procedure at the work place o Review of Batch manufacturing records and batch packing records Job Types: Full-time, Permanent Pay: Up to ₹30,000.00 per month Benefits:
Health insurance
Paid time off
Provident Fund
Schedule:
Day shift
Night shift
Rotational shift
Supplemental Pay:
Overtime pay
Performance bonus
Experience:
total work: 2 years (Preferred)
Work Location: In person
We regret to inform you that this job opportunity is no longer available