We’re looking for a QC Analyst to join our Quality Control team! You’ll play a vital role in ensuring our products meet the highest standards of quality and compliance. Working in a fast-paced, GMP-regulated environment, you’ll help deliver safe and effective medicines to patients worldwide
Perform batch disposition and stability activities, including QC testing and reporting of raw materials, in-process, bulk drug substances, and finished products.~ Act as system owner for QC equipment, overseeing calibration, periodic reviews, and maintenance.~ Prepare, review, and update SOPs, protocols, and other QC documentation in line with Data Integrity standards.~ Maintain QC information systems and ensure accurate records.~ Represent QC in technical meetings and conferences when required.~ Ensure housekeeping and proper maintenance of laboratories and equipment.~ Solid understanding of scientific and technical processes
Experience in a QC laboratory working under GMP conditions. Experience writing, reviewing, and working to SOPs. Knowledge of GMP guidelines and regulatory bodies.
For over three decades, Piramal Group has grown into a global leader through innovation and collaboration. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) with a globally integrated network across North America, Europe, and Asia. We offer end-to-end solutions across the drug lifecycle, from discovery and development to commercial supply, including specialized services in highly potent APIs, ADCs, biologics, gene therapies, and more .
We celebrate diversity and are committed to providing a fair, supportive, and inclusive workplace for all…