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Executive - Quality Assurance, Pharma
Posted on Dec. 25, 2024
- Ankleshwar, India
- 0 - 0 USD (yearly)
- Full Time

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- B. Pharm / M. Pharm from a reputed university
- 1 to 4 years of similar experience in regulatory-approved OSD manufacturing large units.
- Line Clearance and shop floor compliance
- In-process checks and sampling activity
- Assisting in the Complaint Investigation system at the site
- Assisting in Qualification and validation system, change control system, deviations
- Preparing & reviewing the Annual Product Quality Review
- Review of Batch Manufacturing & Packing Records
- Coordination of cGMP Training activity.
- Preparation of quality system SOPs
- Controlled distribution and archival of documents & record
- Control of master documents
- Management of archival room
- Issuance of batch records, ATR, logbooks, and controlled formats.
- In process controls
- Review of Executed Batch Manufacturing & Packing Records
- Ensuring implementation of Corrective actions/Preventive actions proposed in Deviations and Customer complaints
- Ensuring the effectiveness review of the implemented CAPA
- Review of batch records & analytical testing records
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