Browse current jobs

Officer, IPQA

Amneal Pharmaceuticals India · Ahmedabad

Apply on employer website

Source and collection record

Read the employer source

Last observed by our collector: . This is not a manual review or a confirmation from the employer.

Employer requisition: 7490

Job type and experience labels are automated discovery categories. The employer determines eligibility. Original experience wording was not retained separately; check the current employer page.

How sourcing and classification work · Report a discrepancy

Your application evidence checklist

Mark the statements you can support after reading the employer source. This checklist stays on this page; it does not score your eligibility or submit an application.

0 of 3 checks marked. Keep unresolved requirements as questions for the employer.

Collected role description

Department - Quality Assurance - IPQA Designation - Officer / Sr. Officer Qualification - B. Pharm / M.Pharm Experience - 2 to 5 Years Location - Palli Plant Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances, thereby supporting the production of high-quality injectable pharmaceutical products Essential Functions: To ensure cGMP and compliance review in the manufacturing shop floor and packing areas. To supervision of dispensing activity of manufacturing shop floor and packing areas. To Issuance of Bottle label, Ouster and Medication guide for commercial batch. Rsponsible for providing machine and area clearance. To conduct Sampling of reserve sample, stability sample and In-process checks during execution of batch packaging as per Batch Packaging Record (BPR) and stability study protocol. Online Documents and records review like equipment’s logbooks, dispensing logs, housekeeping records, environmental monitoring records, calibration record, batch records etc.. Calibration of IPQA instruments. Additional Responsibilities: Real-time Monitoring and Compliance Reporting. Participation in Investigations. Provide on-the-job training to shop floor personnel on GMP practices, quality standards, and documentation practices. Maintain IPQA-related documents and records in a state of audit readiness. To have good written and verbal communication skills in English language.

Collected minimum qualification

Education: Bachelors Degree (BA/BS) B. Pharm - Required Master Degree (MS/MA) M. Pharm - Preferred 2 - 4 Years

Collected experience requirement

2 years