Quality Assurance Jobs | Par Health is Hiring Quality Assurance Associate | Apply Now
Looking to start or grow your career in the pharmaceutical industry? A full-time Quality Assurance Associate role is now open in Pudupakkam, India, offering a strong entry into regulated manufacturing environments. This opportunity is ideal for candidates seeking quality assurance jobs, QA jobs, and long-term life science jobs in cGMP-compliant pharmaceutical operations.
Job Details
- Job Title: Quality Assurance Associate
- Locations: India – Pudupakkam
- Job Requisition ID: R002772
About the Company
PAR Health is a quality-driven pharmaceutical organization committed to manufacturing safe, effective, and compliant drug products. The company operates under strict cGMP guidelines and focuses on continuous improvement, regulatory compliance, and professional development. PAR Health offers a structured work environment where life science graduates can build strong careers in quality assurance and pharmaceutical manufacturing.
Key Responsibilities
- Organizational Alignment: Align to mission, vision & values of the organization and coach the quality assurance team to develop & sustain behaviors that are consistent with PAR HEALTH values.
- Shopfloor IPQA Activities: Responsible for planning and execution of Shopfloor IPQA activities. Authorize the line clearance during the product changeover in warehouse and production (manufacturing and packing).
- Quality Examination: Conduct quality examination at regular intervals by performing in-process checks during the production process.
- Sampling and Submission: Perform sampling of intermediates, finished drug products, reserve samples & stability samples from manufacturing and packing stages, and submission to the Quality Control unit for testing.
- Hold Time Study Program: Involvement in the hold time study program by performing the sampling and retaining the required sample in controlled storage. Submit samples to the quality control lab at regular intervals as per the sampling plan.
- Compliance and Calibration: Ensure compliance and perform calibration of IPQC-Instruments.
- Environmental Management System: Follow the procedures pertaining to the environmental management system and review EMS alarm history. E-sign with appropriate comments and report any observation/non-conformance related to the environment management system.
- Maintenance Request: Acknowledge maintenance requests and perform the impact assessment before closure.
- Visual Inspection: Conduct visual inspections, destruction of reserve samples, and maintenance of the reserve sample room.
- Product Inspection: Perform product inspection for physical defects as defined in frequency in batch records and ensure compliance.
- Batch Records Review: 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 transactions in SAP.
- Approval and Rejection of Procedures: Approve or reject all procedures impacting the identity, strength, quality, and purity of the drug product. Follow the written procedure applicable to job description.
- Adherence to cGMP: Ensure adherence to cGMP in all activities performed and maintain compliance.
This opening is a valuable opportunity for candidates seeking stable and growth-oriented quality assurance jobs in the pharmaceutical sector. With strong exposure to shopfloor QA, documentation, and compliance systems, these QA jobs provide an excellent foundation for long-term careers in life science jobs and pharma manufacturing.
