Our client is looking for multiple Downstream CQV Engineers to join their team. These engineers will support drug substance manufacturing buildings and help support process equipment. Process Equipment includes, but not limited to Buffer/Media Preparation, Buffer Hold, Chromatography Skids, Chromatography Columns, Column Packing, Ultrafiltration/Diafiltration, Intermediate Bulk Fill, Filtration Skids, Seed and Production Bioreactors.

The engineer will collaborate with cross-functional teams to support the successful delivery of the equipment scope project, ensuring that all operational systems are safe, reliable, and meet the intended design specifications. Support generation and execution of CQV lifecycle documentation including Factory Acceptance Testing (FAT), wraparounds, Design Qualification (DQ), Requirements Trace Matrix (RTM), Quality Risk Assessment (QRA), Site Acceptance Testing (SAT), Installation Qualification, Operational Qualification, Performance Qualification, including Final Reports.

Must Haves:

• Troubleshooting process control systems DeltaV and mechanical aptitude
• Commissioning experience in a startup environment
• Experience with loop tuning
• Minimum of 3 years of Equipment experience including experience construction projects for biopharmaceutical manufacturing facilities.
• Minimum 1-2 years experience in Commissioning and Qualification of Process Equipment on Large Scale Projects
• SME on multiple Process Equipment System types; Upstream, Downstream
• Working knowledge of ASTM E2500 / Leveraging Verification process

Pluses:

• Stainless steel experience (SST) a definite nice-to-have
• Experience with Chromatography
• Process engineering background a huge plus; Chemical Engineering, Mechanical Engineering