CQV Project Manager

Position: CQV Project Manager Location: New England Region Duration: Long Term Job Overview We are seeking a CQV Project Manager to lead Commissioning, Qualification, and Validation (CQV) programs for pharmaceutical and biotechnology manufacturing projects. In this role, you will lead cross‑functional CQV activities, manage project scope, schedules, and client expectations, while driving successful project delivery, quality, and compliance. This is an excellent opportunity to work on state‑of‑the‑art biotech and pharmaceutical manufacturing facilities. Key Responsibilities Lead CQV programs from planning through execution. Manage project scope, schedules, and client expectations. Partner with clients, engineering teams, and project stakeholders. Drive project delivery while meeting quality and compliance objectives. Lead cross‑functional CQV activities throughout the project lifecycle. Support the successful delivery of biotech and pharmaceutical manufacturing facilities. Coordinate with internal and external teams to ensure project success. Maintain effective communication with clients and stakeholders throughout project execution. Required Qualifications Experience leading Commissioning, Qualification, and Validation (CQV) projects. Proven ability to manage project scope, schedules, and client expectations. Experience collaborating with clients, engineering teams, and cross‑functional stakeholders. Strong project management and leadership skills. Excellent communication and stakeholder management abilities. Ability to drive project delivery while maintaining quality and compliance objectives. Experience supporting pharmaceutical or biotechnology manufacturing projects is preferred. #J-18808-Ljbffr