Capital Projects Engineer
PharmEng TechnologyMassachusetts, United States
Posted December 12, 2025
Contract / Temporary
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 highly qualified Capital Projects Engineer to support a strategic, year-long initiative within the Capital Projects group at a major biopharmaceutical facility located in Andover, MA. This role offers significant exposure to site-level capital project planning and execution, with direct responsibility for key elements of design, validation, and implementation in a regulated GMP environment.
Requirements
- Bachelors degree in Engineering or a related technical discipline
- Demonstrated experience in process engineering and equipment validation within a regulated biopharmaceutical or GMP manufacturing environment
- Expertise in equipment validation requirements in accordance with 21 CFR Part 11
- Strong understanding of GMP regulations, capital project execution, and cross-functional collaboration
- Exceptional organizational, communication, and problem-solving skills with a commitment to quality and compliance
Benefits
- Contract (12 Months, Full-Time, Onsite)