Downstream CQV Engineer

Responsibilities: of the Downstream CQV Engineer include: · Execute Installation Verification (IV), Operational Verification (OV), and Performance Qualification (PQ) protocols for downstream manufacturing systems. · Perform field walkdowns, equipment inspections, and P&ID reviews to verify proper installation, configuration, and system readiness. · Support qualification activities for downstream process equipment including chromatography systems, ultrafiltration units, buffer preparation systems, and bulk fill operations. · Utilize DeltaV or similar control systems to execute testing activities, assess system functionality, and assist with troubleshooting during commissioning and qualification efforts. · Prepare, review, and maintain validation documentation while ensuring compliance with GMP requirements and project quality standards. Qualifications: for the Downstream CQV Engineer include: · 2+ years of experience in CQV, validation, process engineering, or related GMP-regulated manufacturing environments. · Experience supporting at least two phases of the qualification lifecycle, including IV, OV, and/or PQ execution. · Strong understanding of downstream bioprocessing equipment and manufacturing operations. · Ability to interpret P&IDs, conduct system walkdowns, and troubleshoot process or mechanical equipment issues. · Experience with DeltaV, Kneat, or similar automation and validation platforms is preferred. · Strong communication, organizational, and technical documentation skills with the ability to succeed in a fast-paced facility startup environment. Compensation: for the Downstream CQV Engineer: · Pay Range: $55-$75/hour · Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K This job opens for applications on 9/25/26. Applications for this job will be accepted for at least 30 days from the posting date.