CQV Engineer

Job Title:CQV EngineersLocation:North Carolina, RTP AreaIndustry:Pharmaceutical/BiotechJob Description:We are seeking experiencedCommissioning, Qualification, and Validation (CQV) Engineersto join a key pharmaceutical project inNorth Carolina. This is a fantastic opportunity to contribute to the qualification of equipment, utilities, and processes in a cutting-edge facility.Key Responsibilities:Lead and execute IQ, OQ, PQ protocols for process equipment and utilities.Perform commissioning and validation activities in compliance with GMP and regulatory standards.Support the development of validation documentation, including protocols, reports, and risk assessments.Collaborate with cross-functional teams to troubleshoot and resolve issues during qualification activities.Ensure compliance with all FDA, GMP, and quality regulations .Requirements:5+ years of experience in CQV within the pharmaceutical/biotech industry .Strong working knowledge of GMP guidelines and validation principles.Hands-on experience with process equipment, utilities, and facility qualification.Proven ability to write and execute validation protocols and reports.Excellent communication and collaboration skills.Details:Contract Duration: 12 monthsWork Schedule: Full-time, on-site in North Carolina, RTP AreaStart Date: Immediate/ASAP

Created: 2026-01-11