Walk-In for Sr. Officer / Officer / Chemist -
QC/QA @ RL Fine Chem Pvt. Ltd
Date
& Time: 13th December - 20th December, 9
AM onwards
Venue:
RLFC House, C-10,
1st Cross, KSSIDC
Industrial Estate,
New Town Yelahanka,
Bangalore-560064
QC- Job Description
- Should have experience in pharma Analytical/Quality Control
- Should have handling knowledge on HPLC & GC Tests
- Should have Knowledge on sampling & wet analysis
- Should have knowledge cGMP/USFDA documentation
- Should have Knowledge on analytical method validation
QA- Job Description
- Issuance and retrievals of Batch Manufacturing records
- Review of the executed Batch Manufacturing records for compliance to the requirements.
- Preparation of Master manufacturing record and Batch Manufacturing records as per technology transfer documents
- Daily rounds and monitoring of the shop floor (Production Warehouse and Engineering) activities to ensure the compliance with requirements
- Coordinate in the dispatch activities and maintain records
- Preparation of data and trend analysis of finished product.
- Assist in the investigation related to Deviation Complaints. OOS & OOT
- Preparation of validation protocols reports
- Change control evaluations
- Line clearance for product changeovers and packaging activities
- Should have experience in pharma Analytical/Quality Control
- Should have handling knowledge on HPLC & GC Tests
- Should have Knowledge on sampling & wet analysis
- Should have knowledge cGMP/USFDA documentation
- Should have Knowledge on analytical method validation
QA- Job Description
- Issuance and retrievals of Batch Manufacturing records
- Review of the executed Batch Manufacturing records for compliance to the requirements.
- Preparation of Master manufacturing record and Batch Manufacturing records as per technology transfer documents
- Daily rounds and monitoring of the shop floor (Production Warehouse and Engineering) activities to ensure the compliance with requirements
- Coordinate in the dispatch activities and maintain records
- Preparation of data and trend analysis of finished product.
- Assist in the investigation related to Deviation Complaints. OOS & OOT
- Preparation of validation protocols reports
- Change control evaluations
- Line clearance for product changeovers and packaging activities
- Additional
activities as assigned by in charge after completion of training
IPQA
Note: No Walk In on Sundays
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