CQV Engineer
PharmEng TechnologyNew Jersey, 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 an experienced and detail-oriented CQV Lead to oversee and execute commissioning, qualification, and validation activities for process equipment and laboratory systems within a GMP-regulated pharmaceutical environment.
Requirements
- 5+ years of experience in CQV within the pharmaceutical/biotech industry
- Solid understanding of GMP regulations, GAMP 5, 21 CFR Part 11, and other relevant guidelines
- Proven experience in writing and executing qualification protocols
- Excellent project management, organizational, and communication skills