Assistant Manager - Quality Control
Job Description:
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Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable).
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Review and approve analytical results, COAs, test reports, and raw data.
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Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.).
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Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.).
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Review and update SOPs, STPs, GTPs, and analytical documentation.
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Manage laboratory investigations—OOS, OOT, deviations, CAPA.
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Coordinate method validation, method transfer, and verification activities.
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Ensure timely sampling and testing of RM/PM, intermediates, finished APIs, and stability samples.
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Support audits (regulatory & customer) and ensure readiness of QC operations.
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Train and supervise QC analysts; ensure adherence to safety practices.
Company Profile
At --- ---, we manufacture, license, and distribute over 400 oral and topical formulations for human and veterinary markets—all under one WHO-GMP-certified roof in Gujarat, India.
High-volume capacity: 2.4 million tablets, 0.5 million capsules, 500Kg semi-solids & 1000 liters Liquids every day
Specialised lines: Bi-layer, effervescent, ODT, controlled-release, powders, oral jellies, creams & ointments
Therapeutic depth: HIV/ARVs, TB, cardiology, CNS, nephrology, OB/GYN, controlled substances & more
Regulatory peace of mind: ACTD/CTD dossiers, COPPs, and full in-house regulatory support
Packaging innovation: combi-kit blisters, liquid/jelly sachets, and custom formats tailored to your market
From concept to commercial launch, our team ensures each batch meets the strictest global standards—while giving you the creative flexibility to stand out.
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.