LL01-030524 Project Manager for CQV Documentation ...
Validation & Engineering Group - Raritan, NJ
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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: * Project Manager for CQV Documentation Project Qualifications: * Bachelor's Degree in Science or Engineering. * 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. * Must be fully bilingual (English / Spanish) with excellent oral skills. * Must be proficient using MS Windows, Microsoft Project and Microsoft Office applications. * Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance. * Available to work extended hours, possibility of weekends and holidays. Skills: * Able to work with multiple projects at the same time. * At least 5 years on the pharmaceutical industry preferably with experience on CQV Projects, Document Control. * Efficient scheduling. * Proactive management. * Project Management experience. Project Scope: The resource should be able to: * Participate in daily meeting/forums regarding the assigned projects. * Participate on change control/events meetings. * Manage change controls to ensure implementation steps are completed on time and in compliance with requirements. * Participate and serve as facilitator and technical support for the CQV Documentation Project. * Report immediately any event of the assigned projects. * Complete event documentation, investigation and closing of implementation actions. * Perform installation and completeness verification of the activities. * Coordinate the activities for the day to ensure compliance with schedule and other project requirements.
Created: 2024-10-22