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We are seeking an experienced Process Equipment Project Engineer – CQV to support equipment specification, procurement, facility integration, and commissioning, qualification, and validation activities for a GMP biopharmaceutical manufacturing project. The consultant will review process equipment requirements, evaluate installation and utility needs, coordinate facility integration, and develop key CQV lifecycle documentation including URS, Design Reviews, and qualification-related documents. The role will work closely with Engineering, Manufacturing, MSAT, Validation, Quality, Facilities, and external vendors to support equipment selection, procurement, installation, and project execution.