About this opportunity
Highbrow Technology Inc lists this CQV Engineer (Onsite/W2) opportunity in raleigh, North Carolina. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Location: Onsite in North Carolina - the RTP area
Client is completing construction of two more DSM units and will be executing final CQV of all equipment, both upstream and downstream.
Focus is going to be operational C&Q of process equipment, automation and associated utilities.
In field verification of all relevant documentation (P&ID’s, data sheets, drawings, etc)
Identification and resolution of startup issues along with any required documentation
Technology environment the consultant will be working in
MS Office
Smartsheet
Kneat
Consultants day to day responsibilities:
Field verification (physical inspection) of P&IDs, equipment datasheets, vendor drawings, isometrics, utility connections, and system boundaries. (Verifying designs match as-built)
Perform system completion walkdowns and turnover package reviews to verify construction readiness, punch list closure, weld documentation, calibration records, and redlines.
Executing commissioning and qualification activities for upstream processes including bioreactors, media prep systems, incubators, pumps, centrifuges.
Executing commissioning and qualification activities for downstream process equipment including chromatography skids, ultrafiltration/diafiltration (UF/DF) systems, viral filtration skids, depth filtration systems, buffer preparation vessels, and product hold tanks.
Field verification and startup testing of chromatography systems: flow path verification, valve sequencing, conductivity monitoring, pressure monitoring, and automation functionality checks.
Verify process alarms, interlocks, emergency shutdown functions, and automation sequences through field testing and control system verification activities.
Execute OQ for automated systems using DeltaV, including loop checks, I/O verification, valve sequencing, interlock testing, alarm challenges, and control logic verification under live conditions.
Identify and resolve startup issues involving automation logic, valve sequencing, cleaning cycle performance, and skid-to-system interfaces.
Required Skills:
Previous experience performing validation (CQV) in a large-scale pharma/life science facility
Examples of required equipment: bioreactors, pumps, centrifuges, UF Skids, chromatography systems, viral filtration systems, buffer prep/hold tanks.
System walkdowns, TOP review, punch list review, calibration record review
Identifying automation logic, valve sequencing, cleaning cycle issues.
Prior experience executing validation activities in a stainless steel and large molecule environment.
Previous experience executing CQV activities on upstream and/or downstream process equipment.
Prior experience doing field verification of P&ID’s, equipment data sheets and vendor drawings.
Prior experience executing OQ activities for the automated systems using DeltaV
Desired Skills:
Process engineer experience (upstream or downstream)
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Worksite address
raleigh, NC, 27601, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.