Hiring CQV Engineer Commissioning Qualification and Validation

Hiring CQV Engineer Commissioning Qualification and ValidationLocation: Pennsylvania PADuration: 9 Month ContractWe are seeking an experienced CQV Engineer to support commissioning qualification and validation activities within a regulated pharmaceutical biotech and medical device environmentKey Responsibilities:Execute Commissioning IQ OQ PQ protocols for equipment utilities and facilitiesDevelop and review validation documents including URS DQ FAT SAT protocols and summary reportsEnsure compliance with cGMP FDA and regulatory standardsCollaborate with Engineering QA Manufacturing and Validation teamsPerform risk assessments deviation investigations and CAPA supportSupport equipment startup troubleshooting and full validation lifecycleMaintain accurate documentation and ensure data integrity practicesRequirements:Bachelor’s degree in Engineering or related field3 plus years of CQV Validation experience in pharmaceutical biotech or medical device industryStrong understanding of GMP environments and validation lifecycleHands on experience with equipment qualification and validationExperience with utilities such as HVAC cleanrooms WFI and clean steam is a plusExcellent documentation and communication skillsPreferred:Experience in sterile or aseptic manufacturing environmentsFamiliarity with validation systems such as Kneat or Veeva