Roles & Responsibilities. Support implementation of a new MES for drug substance manufacturing operations. Contribute across multiple phases including electronic equipment tracking, electronic batch records, and release-by-exception functionalities. Support the Quality Engineering workstream to ensure the site is prepared to adopt and sustain MES capabilities within routine production. Review and support execution and documentation of the CSV Pro...
Company Description. 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. . Job Description. We are seeking a talented, dedicated individual committed to work under the highest ethics standards fo...
Computer Systems Validation Specialist. Who we are. We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and simplify patients’ lives to as many people as possible. With 30 years of technological expertise, we position ourselves as a world leader in sterile single dose with 10 sites on 4 continents and more than 2000 employees. Since 2013, our site Unither Manufacturing LLC. based in R...
