CQV Engineer - Downstream Process Equipment (Biopharma)
PharmEng TechnologyNorth Carolina, United States
Posted December 12, 2025
Full Time
About the Company
PharmEng Technology, now part of the Efor Group, delivers specialized compliance engineering services—Commissioning, Qualification, and Validation (CQV)—to the pharmaceutical, biotechnology, and healthcare sectors, drawing on 25 years of industry expertise. The firm designs, constructs, and validates facilities, utilities, equipment, and computer systems in strict adherence to cGMP, GEP, and GLP, covering areas such as API production, laboratory, and medical device manufacturing. Leveraging Efor’s global network of 3,000 experts across 12 countries, PharmEng combines worldwide best practices with local proximity to offer flexible, innovative, and cost‑effective solutions that meet regulatory and business demands. Its culture prioritizes quality, safety, and client partnership, ensuring customized, measurable outcomes for leading industry players.
Job Description
We are seeking a skilled CQV Engineer to support commissioning and qualification activities for downstream process equipment within a large-scale biopharmaceutical manufacturing facility.
Requirements
- Minimum 5 years of CQV experience in biopharmaceutical manufacturing environments, with a focus on downstream processing systems.
- Strong technical understanding of chromatography, UF/DF systems, filtration, and stainless-steel process equipment.
- Engineering background in Chemical or Mechanical disciplines preferred.
- Experience with DeltaV or similar process control systems, including troubleshooting and loop tuning.
- Familiarity with CQV documentation tools such as Kneat or equivalent.
- Proven ability to work collaboratively in cross-functional teams, including EPCM, automation, QA, and operations.
- Willingness and ability to travel as required for equipment acceptance testing and support.