Qa Executive

Jubilant Pharmova

6 - 9 years

0 Lacs

bharuch

Posted:3 hours ago| Platform:

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Skills Required

good knowledge of cgmp and cglp practices. knowledge of validation process. practical experience in documentation as per various audits.

Work Mode

Work from Office

Job Type

Full Time

Job Description

Role & responsibilities

To prepare Internal Audit/Self Inspection plan.
Perform internal audits to verify compliance with the principles of GMP. Prepare and submit summary of audit findings / audit report.
To record the deviations observed during plant rounds.
Issuance and retrieval of Batch Manufacturing Records.
Control and Issuance of formats.
Ensure that retention of various documents, reports and records are as per documented procedures.
Issue copy of Master Batch Production Instructions to production for batch manufacture & review critical control parameters before release of the batch.
Co-ordination with other department for timely completion of cGMP/ IMS/ FAMI-QS/ HACCP/ process/ quality related documents.
Preparation and review of system based SOPs
Responsible for adherence to EHS policy .
To implement ISO 9000, ISO-14000, OHSAS -18000, TPM and WCM .
To implement of 5S in lab and office.

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