Downstream CQV Engineer

Piper Companies is seeking a Downstream CQV Engineer to join a growing life sciences manufacturing organization for a 6-month contract onsite role supporting large-scale downstream operations based out of Holly Springs, NC. The Downstream CQV Engineer will play a key role in commissioning, qualification, and verification activities across multiple new and existing manufacturing buildings within a greenfield-style environment in the biopharmaceutical industry.

Responsibilities of the Downstream CQV Engineer include:

• Execute Installation, Operational, and Performance Qualification activities for downstream process equipment and systems.
• Perform field-based verification activities including P&ID walkdowns, system turnover, and equipment checks.
• Support software and automation execution efforts, including Operational Verification tied to DeltaV-controlled systems.
• Author, review, and execute qualification documentation while balancing significant on-the-floor execution.
• Troubleshoot equipment and system issues during qualification and support startup activities across DSM facilities.
  
  

Qualifications for the Downstream CQV Engineer include:

• Hands-on experience across at least two of the following: IV, OV, and PQ (IV and OV strongly preferred).
• Background supporting downstream manufacturing operations such as buffer preparation, chromatography, UF, or bulk fill and dispense.
• 2–5 years of experience qualifying large-scale manufacturing or utility equipment in a regulated environment.
• Strong field execution experience with the ability to learn and apply documentation standards and best practices.
• Exposure to DeltaV systems, troubleshooting activities, or greenfield/start-up projects is highly desirable.
  
  

Compensation for the Downstream CQV Engineer:

Salary Range: $75-$85/hr (USD)

Comprehensive Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

This job opens for applications on 5/26/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: CQV, commissioning, qualification, validation, IV, OV, PQ, downstream manufacturing, buffer prep, chromatography, ultrafiltration, UF, DeltaV, automation, P&ID walkdowns, field verification, large-scale equipment, utilities, greenfield projects, biopharmaceutical manufacturing, GMP, Kneat, documentation, troubleshooting, startup support, process engineering, regulated manufacturing.