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Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals. Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies. Validation Engineer (CQV) Location: Raleigh-Durham area, NC Position Overview We are seeking an experienced Validation Engineer (CQV) to support commissioning, qualification, and startup activities for a large-scale biopharmaceutical manufacturing facility. This role will focus on downstream process systems and requires strong hands-on field execution, system troubleshooting, and automation verification experience in a GMP-regulated environment. Key Responsibilities Perform field verification of P&IDs, equipment datasheets, vendor drawings, isometrics, and utility connections to confirm system accuracy and readiness ahead of commissioning and startup. Lead and execute mechanical completion walkdowns and turnover package (TOP) reviews, ensuring construction quality, punch list closure, calibration records, weld documentation, and redline updates are complete. Support commissioning readiness by validating system boundaries, flow paths, and equipment installation in alignment with design documentation. Execute commissioning and qualification (CQV) activities for downstream process equipment including: Chromatography skids Ultrafiltration/Diafiltration (UF/DF) systems Viral filtration systems Depth filtration units Buffer preparation vessels Product hold tanks Perform field startup and functional testing of chromatography systems, including: Flow path verification Valve sequencing checks Conductivity and pressure monitoring Automation functionality validation Conduct Operational Qualification (OQ) testing for automated systems using DeltaV, including: Loop checks and I/O verification Interlock and permissive testing Alarm challenge testing Control logic and sequence verification under live conditions Verify process alarms, interlocks, permissives, and emergency shutdown functions through field execution and control system testing. Perform detailed P&ID walkdowns and field verification of valves, instruments, and process flow to support system turnover, TOP approval, and final acceptance. Identify and troubleshoot startup issues related to: Automation logic and control sequences Valve sequencing and flow path discrepancies Equipment integration and skid interfaces Cleaning cycle performance Collaborate cross-functionally with engineering, construction, and operations teams to maintain project timelines and ensure successful system startup. Required Qualifications Bachelor’s degree in Engineering (Chemical, Mechanical, or related discipline) or equivalent industry experience 5+ years of experience in CQV, commissioning, or validation within biopharmaceutical or life sciences manufacturing Hands-on experience with downstream processing equipment, especially chromatography and filtration systems Strong knowledge of cGMP requirements, commissioning processes, and validation lifecycle Experience executing OQ protocols and field testing activities Familiarity with DeltaV or similar DCS platforms (Emerson experience preferred) Proficiency in reading and interpreting P&IDs, isometrics, and technical drawings Demonstrated ability to work in a fast-paced startup environment with significant field presence Preferred Qualifications Previous experience supporting green