CQV Engineer

Hi
Hope you're doing well.

This is Satya from united Pharma Techmologies. I'have a oepning of CQV Engineer opportunity with one of our pharmaceutical/biotechnology clients in Holly Springs, NC. This is an onsite role supporting final commissioning and qualification activities for new large-scale manufacturing units.

Position: CQV Engineer
Location: Holly Springs, NC

Project Overview:

The project involves commissioning and qualification of upstream and downstream process equipment, automation systems, and associated utilities within a large-scale biologics manufacturing facility.

Key Responsibilities:

• Perform field verification of P&IDs, equipment data sheets, vendor drawings, isometrics, utility connections, and system boundaries.
• Conduct system-completion walkdowns and turnover-package reviews.
• Review punch-list closure, calibration records, weld documentation, and engineering redlines.
• Execute commissioning, IQ/OQ, and operational qualification activities.
• Support DeltaV operational qualification and troubleshooting.
• Identify and resolve equipment startup, automation logic, valve sequencing, and cleaning-cycle issues.

Upstream Equipment:

• Bioreactors
• Media preparation systems
• Incubators
• Pumps
• Centrifuges

Downstream Equipment:

• Chromatography skids
• UF/DF systems
• Viral filtration skids
• Depth filtration systems
• Buffer preparation vessels
• Product hold tanks

Technical Environment:

• DeltaV
• Kneat
• Smartsheet
• Microsoft Office

Ideal Background:

• Strong pharmaceutical, biotechnology, or life sciences manufacturing background.
• Experience with upstream and/or downstream process equipment.
• Experience in large-molecule / biologics and stainless-steel manufacturing environments.
• Hands-on experience with P&ID field verification, system walkdowns, turnover packages, punch lists, and calibration documentation.
• Experience executing DeltaV OQ activities.
• Strong knowledge of GMP commissioning, qualification, and startup activities.