Officer, Quality Control Testing
Amneal Pharmaceuticals · Bharuch · onsite · Posted 41d ago
Undisclosed2–5 yrsfulltimeSourced from
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About this role
Officer - Quality Control is responsible for executing and supporting routine QC laboratory activities, including analysis, documentation, and compliance with cGMP and GLP requirements. The role involves handling raw material, in-process, and finished product testing, supporting stability studies, maintaining instrument compliance, and assisting in deviation/OOS investigations. The position also supports data integrity, SOP adherence, and continuous improvement initiatives within the QC function.
Essential Functions - Officer, Quality Control
- Execute routine preventive maintece, calibration, and verification activities of QC instruments as per approved SOPs.
- Perform analysis and support timely release of raw materials, intermediates, and packing materials as per approved specifications.
- Ensure day-to-day compliance with GLP, safety practices, and laboratory housekeeping requirements.
- Execute stability sample charging, withdrawal, testing, and documentation as per approved stability protocols.
- Support investigation of deviations, OOS, OOAL, and laboratory incidents; assist in implementation of CAPA.
- Prepare, revise, and follow QC-related SOPs, test methods, and specifications; ensure compliance in routine work.
- Perform audit trail checks and ensure adherence to data integrity requirements for computerized systems.
- Enter, verify, and maintain accurate analytical data and sample status in LIMS.
- Participate in training programs and support knowledge sharing within the QC team.
- Maintain analytical columns, reference standards, and laboratory consumables as per SOPs.
- Perform analysis and support timely release of raw materials, intermediates, and packing materials as per approved specifications.
- Ensure day-to-day compliance with GLP, safety practices, and laboratory housekeeping requirements.
- Execute stability sample charging, withdrawal, testing, and documentation as per approved stability protocols.
- Support investigation of deviations, OOS, OOAL, and laboratory incidents; assist in implementation of CAPA.
- Prepare, revise, and follow QC-related SOPs, test methods, and specifications; ensure compliance in routine work.
- Perform audit trail checks and ensure adherence to data integrity requirements for computerized systems.
- Enter, verify, and maintain accurate analytical data and sample status in LIMS.
- Participate in training programs and support knowledge sharing within the QC team.
- Maintain analytical columns, reference standards, and laboratory consumables as per SOPs.
Qualifications
Education
- M.Sc / M.Pharm / B.Pharm - Chemistry or related discipline preferred.
Experience
- 1-5 years of hands-on experience in QC operations within an API manufacturing facility.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
API ManufacturingCGMPProduct testingtraining programsChemistryCAPARaw MaterialStability StudiesQuality ControlManufacturingoperationsmaintenancePreventive MaintenancecomplianceQCHousekeeping
About Amneal Pharmaceuticals

Amneal Pharmaceuticals
Pharma
5.5k+
employees
2002
24 years old
Bridgewater, New Jersey
United States (USA)
About
Amneal Pharmaceuticals operates in the pharmaceutical sector, focusing on developing accessible and affordable medicines to address critical healthcare challenges.
Industries
PharmaBiotechnologyClinical Research
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1,455 reviews
4.2/ 5
Culture
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