Commissioning Engineer

Overview Intellectt is looking for Medical Device Quality Assurance professional for W2 contract role onsite at Massachusetts. Senior Commissioning / Startup Engineer — 5–10 Years. Location: Onsite – Indianapolis. Industry: Pharma (Capital Projects / Utilities / Automation). 6-12 Months. Responsibilities Lead commissioning and startup execution for pharma utility and process systems. Develop and review operation verification (OV/OQ) test scripts, startup logic, and turnover strategy. Lead startup activities including flushing, pressure testing, system energization/livening, and readiness reviews. Oversee installation verification, operational verification, and PQ support activities. Coordinate with construction, automation, validation, QA, and vendors to resolve issues. Enforce LOTO procedures and site safety compliance. Manage punch lists, deviations, and commissioning documentation. Support DeltaV-based systems where applicable (FAT/SAT, integration, troubleshooting). Required Experience 5–10 years commissioning/startup experience in pharma or large-scale regulated capital projects. Strong background in utility systems startup and handover. Proven experience leading field execution and commissioning teams. Deep understanding of IV/OV/OQ execution and documentation. Full-time onsite availability in Indianapolis. #J-18808-Ljbffr