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Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
The CQV Specialist will support the commissioning and qualification of downstream process equipment for a GMP-compliant biotechnology manufacturing facility. The role involves hands-on execution of IQ/OQ/PQ protocols, system walkdowns, and validation documentation for equipment such as chromatography skids, TFF systems, ultrafiltration units, centrifuges, and bioburden reduction filtra...
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