Key Responsibilities

- Perform routine analysis of raw materials, in-process samples, finished products, and stability samples.
- Operate and maintain analytical instruments such as HPLC, GC, IR, and ICP-OES .
- Conduct routine chemical testing , limit tests , and titration analysis as per approved analytical methods.
- Perform calibration and verification of laboratory instruments as per SOPs.
- Prepare, review, and maintain QC documentation, analytical reports, logbooks, and laboratory records.
- Ensure compliance with GMP, GLP, Data Integrity (ALCOA+), and regulatory requirements.
- Investigate OOS/OOT results, laboratory deviations, and implement corrective actions.
- Troubleshoot analytical instruments and coordinate with service engineers when required.
- Follow laboratory safety practices and maintain a clean and organized work environment.
- Coordinate with QA, Production, and other departments to ensure timely testing and product release.

Required Skills & Experience

- Hands-on experience with HPLC, GC, IR , and knowledge of ICP-OES .
- Experience in routine chemical testing , limit tests , and titration analysis .
- Experience in calibration of laboratory instruments .




- Strong knowledge of GMP, GLP, Data Integrity , and regulatory compliance.
- Valuable understanding of QC documentation, SOPs, and laboratory practices.
- Strong analytical, troubleshooting, and problem-solving skills.
- Excellent attention to detail and documentation practices.
- Good communication and teamwork skills.
- B.Sc./M.Sc. Chemistry, B.Pharm, M.Pharm, or an equivalent qualification.
- Experience in Quality Control (QC) within Pharmaceutical, Ayurvedic, or Nutraceutical manufacturing .
- Hands-on experience with HPLC, GC, IR , and routine laboratory testing.
- Strong understanding of GMP/GLP , Data Integrity, and regulatory guidelines.
- Experience in instrument handling, calibration, documentation, and troubleshooting.
- Ability to work independently as well as in a team environment.

Preferred Experience

- Experience with pharmacopoeial testing (IP, USP, BP, EP) will be an added advantage.
- Exposure to regulatory audits and quality management systems is preferred.

How to Apply

Pay: ₹300,000.00 - ₹600,000.00 per year

Work Location: In person

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