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Job description
Join our QC team with a quality mindset to help make and release medicines for better lives. Our team is built on trust, respect, and integrity. The quality mindset is about operating with reliability, efficiency, and honest feedback.
Laboratory role to support the qualification, and validation of analytical methods for biologic drugs and process related impurities. Execute Analytical Development activities, investigations, and data evaluation in a GMP environment to ensure compliance based on regulatory and industry standards.
Strong hands-on experience operating and troubleshooting Cytiva based Biacore systems using Biacore Insight required. Strong understanding of molecular biology assays in support of product quality testing for Biologics drug substances/drug products.
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Healthcare • Manufacturing
Rentschler Biopharma is a leading contract development and manufacturing organization (CDMO) specializing in biopharmaceuticals, offering end‑to‑end services that span cell line and process development, formulation, analytics, quality control, regulatory support, and GMP manufacturing through to commercial supply. Leveraging a robust quality management system and an operational‑excellence philosophy, the company delivers technology‑driven solutions that accelerate product development and ensure high‑quality biologics. With approximately 1,400 employees, Rentschler Biopharma is a family‑owned firm headquartered in Laupheim, Germany, and operating a U.S. site in Milford, Massachusetts. Its expertise and global footprint make it a trusted partner for biopharma clients seeking reliable, high‑performance development and manufacturing capabilities.