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 [Confidential Information]
- Salary Best in Industry
- EXPERIENCE NEED Minimum 2 Years
