CQV EngineerContract: 12 Months (Potential for Extension)Type: Full-time, On-siteOverviewWe are seeking an experienced CQV Engineer to support a broad range of capital and site-based projects. This role will work across both the Projects and Validation departments, collaborating closely with existing CQV engineers and cross-functional teams. The successful candidate will bring a wide range of CQV expertise and the flexibility to adapt to diverse project scopes.ResponsibilitiesDeliver commissioning, qualification, and validation (CQV) activities across multiple projects simultaneously.Support upgrades and modifications to utilities, process equipment, filling/packaging lines, and laboratory facilities.Collaborate with both the Projects and Validation departments to ensure alignment of CQV deliverables.Interface with other CQV engineers, both broad-based and specialist, to ensure project goals are met.Prepare and execute CQV documentation in compliance with internal standards and regulatory requirements.Provide technical support during new product introduction, scale-up, and clinical supply projects.Participate in project meetings, providing CQV input and updates.Ensure timely completion of CQV tasks to meet project schedules.RequirementsMinimum 5 years' experience within the pharmaceutical industry.Proven background in commissioning, qualification, and validation across:Process equipmentUtility systemsFill/pack systemsStrong understanding of GMP and regulatory compliance standards.Ability to work across multiple teams and manage competing project priorities.Excellent communication and problem-solving skills.Ability to adapt quickly to different project scopes and requirements.Additional InformationReporting line to the Projects or Validation Manager.Interviews will be conducted in one stage (with potential for a second round)Start date targeted for early in the new year.