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4.0 - 6.0 years
5 - 6 Lacs
Navi Mumbai
Work from Office
Job Description 1 Master & Control of all documents like SOPs, BMR, Specification & MOA, logbooks, calibration records to concern departments. 2 Issuance of all documents like SOPs, BMR, Specification & MOA, logbooks ,calibration records to concern departments 3 Preparation of all documents like SOPs, BMR, Specification & MOA, logbooks, calibration records of concern departments 4 Reviewing of HPTLC, TLC, GC reports, peaks, graphs etc 5 Checking & signing of BMR of Liquid syrup, Tablets & Mother tincture section. 6 Receipt & storage of executed documents like BMR, Analytical logbooks, calibration records etc. 7 Receipt & storage of control samples of finished product, raw material etc. 8 Receipt, storage & destruction of superseded SOPs. 9 Preparation of process validation protocol & Report. 10 Receipt & storage of executed validation protocol & Report 11 Receipt & storage of executed Qualification documents of equipment & instruments 12 Stability studies documentation with help of Quality control. 13 Preparation & Revision of SOPs of Quality Assurance department. 14 Compliance and preparation of Audit Report. 15 Maintenance of control sample room & Documentation room. 16 Training of sub ordinates & evaluation. 17 Preparation of Training schedule and its implementation and monitoring. 18 Identification of training needs to internal/ external to the sub ordinates. 19 Compliance of Audit Report from Government authorities (FDA). 20 Any other activity assigned by the management.
Posted 2 weeks ago
7 - 11 years
2 - 4 Lacs
Noida
Work from Office
Ensuring compliance with Current GLP, Collaborate other internal department, Lab Qualification, Vendor Qualification & CMS Verification, Check the Artwork, Product Inspection Report, Check ADC document, SOPs of QA. Share CV on jobs@asmohlab.com Required Candidate profile Manage Control Sample, Document Controlling, Risk Assessments related to Product Quality, Supply Chain & Regulatory Compliance.
Posted 2 months ago
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