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Driving all aspects of purification process development, characterization, and technology transfer to cGMP manufacturing for hybrid and continuous processes; Serving as an internal technical resource for cGMP manufacturing and Process Design as well as a
This person will join a fast-paced, collaborative, and multidisciplinary team to support purification process development at the bench and pilot scale for the advancement of low-cost biotherapeutics manufacturing. Experience with high throughput
Overseeing the overall end to end COE Research group covering pDNA, mRNA & Delivery (including Lipids discovery, associated synthesis) research teams and capabilities supporting Sanofi ambition in the field of therapeutic and prophylactic approaches