QC Chemist Executive
Job Description:
Key Responsibilities:
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Perform analysis and testing of Raw Materials (RM), Packaging Materials (PM), in-process samples, finished products, and stability samples as per pharmacopoeia standards.
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Operate, calibrate, and maintain analytical instruments such as HPLC, GC, UV, IR, Dissolution Apparatus, etc.
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Ensure timely release of materials/products with accurate and complete documentation.
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Maintain records, calibration logs, data integrity, and adherence to SOPs.
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Follow cGMP, GLP, and regulatory compliance in the QC laboratory.
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Handle OOS / OOT results, deviations, lab incidents, and prepare required reports.
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Prepare and review STPs, COA, specifications, and test reports.
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Coordinate with QA, Production, and Warehouse teams to ensure smooth operations and timely batch release.
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Support internal and external audits such as WHO / USFDA / MHRA / etc.
Desired Profile / Criteria / Skills :
Requirements:
- B.Sc./M.Sc. Chemistry or B.Pharm/M.Pharm.
- Hands-on experience in RM/PM analysis (3–6 years).
- Knowledge of pharma guidelines (IP, BP, USP).
- Strong documentation and compliance skills.
- Gujarati-speaking preferred.
- QC: 1 year (Preferred)
Offered Benefits / Facilities :
Why Join Us?
- Exposure to regulated pharma environment.
- Professional growth in a leading formulation company.
- Supportive work culture with career stability.
Key Skills :
Company Profile
Our client followa standards of WHO - CGMP
Our Mission
“To become a valued Pharmaceutical partner to the World Pharma fraternity by continuously researching, developing and manufacturing a wide range of pharmaceutical products that complies with the global regulatory standards.”
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.