Andhra Pradesh / Hyderabad

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Key Responsibilities

- Perform analysis of raw materials, in-process samples, finished products, and stability samples as per approved specifications.

- Conduct in-process quality checks during manufacturing to ensure compliance with quality standards.

- Perform analytical testing using HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution Apparatus, and other laboratory instruments.

- Review and document analytical results in accordance with GLP and data integrity requirements.

- Prepare and maintain laboratory records, logbooks, test reports, COAs, and analytical worksheets.

- Ensure compliance with cGMP, GLP, SOPs, STPs, pharmacopeial standards (IP, USP, BP, EP), and regulatory guidelines.

- Handle OOS (Out of Specification), OOT (Out of Trend), deviations, and laboratory investigations with appropriate CAPA implementation.





- Perform calibration, verification, and routine maintenance of laboratory instruments.

- Maintain reference standards, reagents, volumetric solutions, and laboratory inventory.

- Participate in method validation, method verification, and stability studies.

- Support internal, customer, and regulatory audits (USFDA, MHRA, WHO-GMP, EU GMP, etc.).

- Coordinate with Production, QA, Warehouse, and Engineering departments for quality-related activities.

- Ensure laboratory safety, housekeeping, and compliance with EHS requirements.

- Location Andhra Pradesh / Hyderabad

- Website [email protected]

- Salary Best in Industry

- EXPERIENCE NEED Minimum 2 Years

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