
Executive C QA
1 week ago
**Experience -** 5+ Years
**Education -** MSC
**Gender -** Male
**Job Location -** Lonavala
**About Role **-**
- Preparation, review and revision of Standard Operating Procedure and Integrated QMS documents ensure training.
- Verification of Implementation with respect to cGMP system for manufacturing operations
- To support in Handling Regulatory and Non regulatory inspections.
- To carry of Compliance action post audit.
- To carry out self-inspections, issuance, review and their closure.
- To review all executed quality related controlled documents like quality procedures, SOP’s, BMPR’s and specifications etc.,
- Preparation and review of technical agreements.
- Review and compilation of calibration, validation protocols and reports.
- To perform vendor qualification, Review Vendor Qualification set and preparation of vendor list.
- Archival and retrieval of documents.
- Verification of control documents, issuance and their retrieval.
- Preparation, review, compilation and execution of PQR.
- Handling of change control and deviations, issuance, review and their closures.
- Handling of corrective and preventive actions, issuance, review and their closure.
- Assignation of numbering system to BMPR.
- To carry out in process Quality Checks.
- Handling of market complaints, investigation, completeness and closure.
- Vendor Qualification data verification and generation of item codes.
- To arrange and provide departmental trainings as per Training Calendars.
- To perform the Job assigned by Dept. Head in absence of Officer in the QA Dept., if any.
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