QA Executive ( (QMS documentation )

QA Executive ( (QMS documentation )

1 Nos.
61077
Full Time
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.50 LPA
Production / Quality / Maintenance
Pharma/Biotech/Clinical Research
B.Pharma - Pharmacy; M.Pharma - Pharmacy
Job Description:

Duties & Responsibility :
·       Quality Management System Implementation and Modification control.
·       Document Control.
·       Approval for batch release.
·       Review and approval of Qualification Document.
·       Review and approval of Calibration and Validation document.
·       Planning, execution and compliance of both internal and external audits.
·       Preparation of audit compliance report
·       Review and approval ofSMF, VMP and Quality manual.
·       Review and approval of BMR, BPR, MFC.
·       Review and approval of OOS/OOT.
·       Review and approval of Vendor list.
·       Planning, execution and compliance of both internal and external-audits.
·       Review and approval of all Quality Assurance, quality Control and manufacturing records.
·       Review of filled BMR/BPR and analysis data, and release of batch for dispatch.
·       Review and approval of SOPs.
·       To prepare audit and compliance reports and CAPA reports.
 

Company Profile

Our Client is a reputed pharma company based at Vadodara

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