Hyderabad / Visakhapatnam

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Key Responsibilities

- Review and approve analytical documents such as STPs, specifications, and reports.
- Ensure compliance of QC laboratory activities with GMP, GLP, and data integrity principles.
- Review analytical data, test results, and certificates of analysis (COA).
- Handle OOS, OOT, deviations, and CAPA related to QC/analytical activities.
- Audit laboratory records, logbooks, and instrument usage.
- Ensure calibration and qualification status of analytical instruments.
- Support method validation, transfer, and verification activities.
- Participate in internal audits and regulatory inspections (USFDA, WHO, EU GMP).
- Ensure proper documentation and control of records as per GDP practices.
- Coordinate with QC, Production, and other departments for quality compliance.
- Location Hyderabad / Visakhapatnam
- Website [email protected]
- Salary Best in Industry
- EXPERIENCE NEED Minimum 2 Years (Relevant Sector)

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