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Senior Officer, QC Testing at Amneal India
, gujarat, India -
Full Time

Start Date

Immediate

Expiry Date

10 Jun, 26

Salary

0.0

Posted On

12 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Quality Control, Preventive Maintenance, Calibration, Verification, GLP, Safety Practices, Stability Testing, Deviation Investigation, OOS Investigation, CAPA Implementation, SOP Preparation, Test Method Development, Data Integrity, LIMS, Analytical Testing, API Manufacturing

Industry

Pharmaceutical Manufacturing

Description
Essential Functions – Sr. Officer, Quality Control • Execute routine preventive maintenance, 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.
Responsibilities
The Senior Officer is responsible for executing routine Quality Control laboratory activities, including instrument maintenance, analysis of raw materials and intermediates, and managing stability studies according to approved protocols and SOPs. This role also involves supporting investigations into deviations and OOS results, ensuring compliance with cGMP and GLP standards, and maintaining accurate data integrity.