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Aetea Information Technology |
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PM with validation, glp, cfrPosted: November 16, 2009
Client is looking for a hybrid PM who can work on both large and small scale projects. They should be able to do hands on validation and understand the life cycle of drug. Must understand regulations. The position involves providing Project Management services to a medium-to-large IT project in a GLP regulated environment using the standard Project Management best practices of the company. Requires significant collaboration and coordination of multiple functional areas and geographic sites. A substantial portion of the job involves the timely creation and editing of quality, readable complex technical documentation that requires practical understanding of regulatory requirements, especially 21 CFR Part 58 and 21 CFR Part 11, Systems Development Life Cycles, and Systems Validation. Please refer to job code cmd329 when responding to this ad.
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