Chemistry QC Job at Amneal | Candidates Apply Now
Are you looking for a Chemistry QC Job in a reputed pharmaceutical company? Here’s an excellent opportunity with Amneal Careers! Amneal Pharmaceuticals is hiring an Officer – Quality Control Testing in Dahej, Gujarat. This Amneal Job is ideal for candidates with hands-on QC experience in API manufacturing and a strong understanding of GLP, cGMP, and laboratory practices.
About Amneal
Amneal Pharmaceuticals is a leading global pharmaceutical company known for developing, manufacturing, and distributing a wide range of generic and specialty medicines. With a strong presence in India and international markets, Amneal Careers provides excellent growth opportunities for professionals in Quality Control, R&D, and manufacturing. Working at Amneal means being part of a company that values innovation, compliance, and continuous improvement—making it an ideal destination for candidates seeking a stable and rewarding Chemistry QC Job.
- Position: Officer, Quality Control Testing
- Location: Dahej SIR, Gujarat, India
- Job Identification: 7460
This Chemistry QC Job under Amneal Careers offers a great platform to work in a regulated pharmaceutical environment.
Job Description
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 maintenance, calibration, and verification activities of QC instruments as per approved SOPs.
- Perform analysis and support the 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.
