CQV Engineer

Are you an experienced CQV Engineer looking to join a dynamic project team delivering complex pharmaceutical or life sciences projects? We are seeking a driven and collaborative CQV professional to support commissioning, qualification and validation activities across a range of GMP regulated systems, facilities and equipment. This is an excellent opportunity to work on high impact projects in a fast paced and technically challenging environment. Key Responsibilities Execute Commissioning, Qualification and Validation (CQV) activities in line with project schedules and GMP requirements. Support commissioning, startup and qualification of equipment, utilities and process systems. Prepare, review and execute validation documentation including protocols, reports, and traceability matrices. Lead or participate in design reviews, FATs, SATs, commissioning, IQ, OQ and PQ activities. Manage qualification documentation through the full CQV lifecycle. Coordinate activities with engineering, operations, quality, contractors and equipment vendors. Track progress, identify risks and support timely project delivery. Assist with change controls, deviations, punch lists and documentation management. Ensure all activities are performed to the highest safety and compliance standards. Provide technical support during project execution and system handover What We're Looking For Experience within Pharmaceutical, Biotechnology, Medical Device or Life Sciences industries. Background in Commissionin