Quality Assurance Senior Associate at Endo

Tiruporur, tamil nadu, India -

Full Time

Start Date

Immediate

Expiry Date

25 Sep, 26

Salary

0.0

Posted On

27 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

In-Process Quality Assurance, Line Clearance, Sampling, cGMP Compliance, SAP, Environmental Management System, Batch Record Review, Calibration, Visual Inspection, Quality Control

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary Responsible for planning and Execution of Shopfloor IPQA activities. Responsible for Authorizing the Line Clearance during the product change over in warehouse and production (manufacturing and packing ). Responsible for Conducting quality examination in regular intervals by performing in-process checks during the production process. Job Description Responsible for planning and Execution of Shopfloor IPQA activities. Responsible for Authorizing the Line Clearance during the product change over in warehouse and production (manufacturing and packing ). Responsible for Conducting quality examination in regular intervals by performing in-process checks during the production process. esponsible to perform Sampling of intermediates finished drug products, Reserve samples & stability samples from manufacturing and Packing stages and submission to Quality Control unit for testing. Responsible for Involvement in hold time study program by performing the sampling and retaining the required sample in controlled storage. Submission of sample to quality control lab on regular intervals as per sampling plan. Responsible for ensuring the compliance and performing calibration of IPQC-Instrument. Responsible for to follow the procedures pertaining to the environmental management system and review of EMS alarm history, e-sign with appropriate comments. Report any observation/non-conformance related to the environment management system. Responsible for Acknowledgement of Maintenance request and performing the impact assessment before closure. Responsible for performing visual inspection, destruction of reserve sample and Maintenance of reserve sample room. Responsible for performing product inspection for physical defects as defects as defined frequency in batch record and ensuring the compliance. Responsible for review batch records to assure that no errors have occurred or, if errors have occurred, that they have been fully investigated. Responsible for release the bulk, Posting sample quantity and other QA associated transaction in SAP. Responsible for approving or rejecting all procedures impacting on the identity, strength, quality, and purity of the drug product. Responsible for follow the written procedure applicable to job description. Responsible for to adherence of cGMP in all activities performed and responsible for compliance. Come join us! At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.

Responsibilities

Responsible for planning and executing shopfloor IPQA activities, including line clearance and in-process quality checks during production. Manages sampling of drug products, calibration of IPQC instruments, and ensures strict adherence to cGMP and environmental management systems.