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LL Project Manager for CQV Documentation Project
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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.
- Minimum of 5 years of experience in Project Management in direct pharmaceutical, medical device or biotechnology industries.
- Experience in CQV in direct pharmaceutical, medical device or biotechnology industries.
- Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
- At least 5 years on the pharmaceutical industry preferably with experience on CQV Projects, Document Control.
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