Senior Officer/Executive
16 hours ago
Roles & Responsibilities:
- Conduct routine analysis of raw materials, in-process samples, and finished products as per approved specifications and procedures.
- Provide timely analytical support to the production department to ensure smooth and uninterrupted manufacturing operations.
- Perform chemical and instrumental analysis (HPLC, GC, UV, IR, titrations, etc.) as required.
- Ensure all analytical data, test results, and observations are accurately documented in accordance with Good Laboratory Practices (GLP).
- Maintain calibration and validation records of laboratory instruments.
- Assist in investigation of non-conforming results, deviations, and OOS (Out of Specification) findings.
- Support implementation of GMP, GLP, and other quality systems in the laboratory.
- Participate in stability studies and ensure samples are analyzed as per stability protocol.
Coordinate with QA and Production for timely release of batches and documentation compliance.
Ensure safe laboratory practices and proper disposal of chemical waste.
Preferred Candidate Profile:
- M.Sc. in Chemistry, Biochemistry, or related discipline.
- 25 years of experience in Quality Control (Analytical) in a manufacturing setup (preferably pharmaceuticals, chemicals).
- Hands-on experience with analytical instruments such as HPLC, GC, UV-Vis spectrophotometer, pH meter, etc.
- Strong understanding of GMP, GLP, and documentation practices.
- Good analytical and troubleshooting skills with attention to detail.
- Ability to work collaboratively with production and quality teams.
- Good communication, time management, and organizational skills.
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