Quality Control Job at Amneal Pharmaceuticals | MSc Chemistry Job
Looking for Quality Control Jobs in Gujarat? Here’s an exciting opportunity under Amneal jobs for the role of QC Officer. This opening is ideal for candidates searching for M.Sc Chemistry Jobs and pharma QC roles in API manufacturing. If you have experience in GLP, GMP, and laboratory analysis, this is your chance to build a strong career in the pharmaceutical industry.
About Amneal Pharmaceuticals
Amneal Pharmaceuticals is a leading global pharmaceuticals company dedicated to innovation, quality, and service satisfaction. We strive to foster a work environment that promotes collaboration, curiosity, and growth. Join us as we push the boundaries of medicine and healthcare. This opportunity is with Amneal Pharmaceuticals, a globally recognized company in the pharmaceutical sector known for its high-quality API manufacturing and strong compliance standards. Amneal jobs offer excellent career growth, innovation, and a professional work environment for chemistry and pharmacy graduates.
- Job Title: Officer, Quality Control
- Location: Dahej SIR, Gujarat, India
- Job Identification: 7456
Requirements
- Education: M.Sc / M.Pharm / B.Pharm – Chemistry or related discipline preferred.
- Experience: 1-6 years of hands-on experience in QC operations within an API manufacturing facility.
Job Description
The 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.Responsibilities
- 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.
