Posted:2 days ago|
Platform:
On-site
Full Time
Production-Packing- Injection
· Allocations of workman / manpower in area & supervision of activities going in area.
· Following of gowning procedure as per SOP & ensuring for subordinate also.
· Ensure calibration of equipment’s / instruments, etc.
· Preparation of line clearance & taking line clearance before start in designated working areas.
· To supervise and monitor activities in general Tablet area pertaining to Dispensing, Granulation, Compression, Coating, Inspection & Packing
· Compliance to CGMP practice in documents, area, daily logs and its timely completion as per the defined schedule in SOP.
· Best utilization of man, material and machineries.
· Completing online BMR / BPR, formats & ensuring its timely updating.
· Checking / Ensure continuous quality through IPQC checks
· Ensure for adherence & compliance of Maintaining / follow CGMP practices in workplace.
· Ensure / checking environmental conditions like temperature / humidity & recording differential pressure etc. in the area.
· Follow & ensure the labeling procedure as per SOP in the area & segregation of Product / Batch wise to avoid mix-up.
· Checking & ensuring personnel hygiene & Safety.
· Checking & ensuring the cleaning of equipment’s as per SOP & cleaning and sanitization practices in production / packing area as per SOP.
· To follow standard operating procedures / manufacturing, packing procedure as per BMR /BPR by own & also by workmen.
· Proper storage of spares / equipment’s, issuance & checking of materials.
· Controlling quality / yield at each stage of operation as per limits specified.
· Filling & Reconciliation in BMR /BPR.
· Ensure Storage of product / Raw materials as per storage condition during processing / storages.
· Ensure the removal of scrap from the area with proper status label.
· Adhere and follow Quality Policy of Organization.
· Ensure and follow proper segregation of waste.
· Maintaining day-to-day wise production report.
· Routinely coordination to other department for maintenance (utilities/ services) like in case of breakdown, Quality Assurance, Quality control, Human Resources, PPIC wherever required.
· Checking availability of documents where required.
· Preparation & recording of documents as required.
· Following safety protective clothing, availability & implementation as defined.
· Raising BMR /BPR request as per requirement.
· Doing correct entries in Pharm cloud wherever required.
· Control of rejection at each stage of operation.
· To train sub-ordinates as and when required.
· Any other Job assigned by Department Head or seniors.
Job Type: Full-time
Benefits:
Bharat Parenterals Limited
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