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Endo Pharmaceuticals is hiring Quality Assurance (IPQA) Associates and Senior Associates for its Chennai facility. This opportunity is ideal for experienced IPQA professionals with strong exposure to in-process quality assurance, cGMP compliance, and pharmaceutical manufacturing operations.
If you are looking to advance your career in Quality Assurance IPQA jobs in Chennai, this role offers hands-on responsibility, regulatory exposure, and long-term career growth in a regulated pharma environment.
📌 Job Overview
- Position: Associate & Senior Associate – Quality Assurance (IPQA)
- Department: Quality Assurance – IPQA
- Experience: 3 to 7 Years
- Location: Chennai, Tamil Nadu
- Qualification: B.Pharm / M.Pharm
🔍 Key Responsibilities – IPQA Roles & Responsibilities
- Authorize line clearance during product changeover in warehouse, manufacturing, and packing.
- Perform in-process quality checks at defined intervals during production.
- Execute sampling of intermediates, finished products, reserve samples, and stability samples.
- Submit samples to Quality Control (QC) as per approved sampling plans.
- Support hold time studies by sampling and storing materials under controlled conditions.
- Ensure calibration and compliance of IPQC instruments.
- Monitor Environmental Management System (EMS) alarms, review history, and document e-signatures with observations.
- Acknowledge maintenance requests and perform impact assessments prior to closure.
- Conduct visual inspection, reserve sample destruction, and maintenance of reserve sample rooms.
- Inspect products for physical defects as per batch record frequency.
- Review batch manufacturing and packing records for accuracy and compliance.
- Release bulk materials and perform QA transactions in SAP.
- Ensure strict cGMP, data integrity, and regulatory compliance in all activities.
🎓 Eligibility Criteria & Skills
- B.Pharm or M.Pharm from a recognized institution.
- 3–7 years of experience in IPQA / In-Process Quality Assurance.
- Strong knowledge of cGMP, SAP, batch record review, and pharmaceutical documentation.
- Experience in OSD / manufacturing / packing operations preferred.
- Good understanding of regulatory and quality systems.
💼 Salary & Benefits
- Salary Range: ₹4,00,000 – ₹8,00,000 per annum (CTC)
- Performance-linked growth opportunities
- Exposure to regulated manufacturing environments
- Professional development and compliance training
📩 How to Apply
Interested and eligible candidates can share their updated CV at:
📧 Nagarajan.patchaiappan@endo.com