Validation Engineer
PharmEng TechnologyHouston, Texas, 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 detail-oriented and experienced Validation Engineer to support pharmaceutical manufacturing validation projects. The role focuses on the execution, review, and documentation of Installation and Operational Qualification (IOQ), Performance Qualification (PQ), and related validation activities for critical systems and equipment including TOC analyzers, purified water systems, autoclaves, steam generators, clean rooms, and utilities.
Requirements
- Bachelor's degree in Engineering, Pharmaceutical Sciences, or related technical field.
- Proven experience in pharmaceutical manufacturing validation, including hands-on execution of IQ/OQ/PQ protocols.
- Strong understanding of CGMP, FDA, EMA regulations, and GMP validation requirements.
- Knowledge of utilities, critical manufacturing systems, and laboratory instruments (e.g., TOC analyzers, purified water systems, autoclaves).
- Experience with technical documentation, deviation handling, and change control processes.
- Excellent organizational skills and attention to detail in documentation and report generation.
- Ability to work independently and as part of a project team under contract terms.