Engineering Document Specialist
PharmEng TechnologyMassachusetts, 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 looking for a motivated Engineering Document Specialist to join our team and support documentation and records management activities in a regulated environment. The successful candidate will partner with cross-functional teams, organize and manage project turnover packages, and collaborate with colleagues to ensure documentation meets compliance and business standards.
Requirements
- Bachelor's degree (or equivalent experience)
- Strong attention to detail and organizational skills
- Ability to manage multiple tasks independently while being a great team player
- Interest in learning cGMP, quality systems, and documentation processes
- Clear written and verbal communication skills
- A proactive mindset with curiosity to ask questions and solve problems