{"schemaVersion":"jobsearcher.job.v1","id":"7db1aa0d77fa8a496c6250f6","url":"https://jobsearcher.com/jobs/7db1aa0d77fa8a496c6250f6","canonicalUrl":"https://jobsearcher.com/jobs/7db1aa0d77fa8a496c6250f6","title":"Facilities Engineer","description":"We are seeking an experienced Facilities Engineer – CAD Support to join a leading life sciences organization in Plainville, MA. This role will support Facilities Engineering by managing engineering documentation, CAD services, and the site's spare parts program while ensuring compliance with cGMP and quality standards.Key ResponsibilitiesManage and maintain GMP and Non-GMP engineering drawings and documentation.Serve as the primary liaison between Facilities Engineering, Project Management, Validation, and Quality teams.Maintain engineering documentation using the Adept Documentation System (EDMS).Update, revise, and manage engineering drawings utilizing the Adept CAD system.Develop and maintain procedures for engineering documentation and periodic drawing reviews.Manage the site's spare parts program, including inventory planning and risk assessments for critical facility, utility, and process equipment.Support Change Controls, CAPAs, Deviations, and engineering documentation updates.Maintain CMMS work orders and engineering drawing records (Blue Mountain preferred).Ensure engineering documentation is audit-ready and supports internal and regulatory inspections.Oversee contractor documentation activities to ensure compliance with site standards.Required QualificationsBachelor's degree in Engineering or a related technical discipline (or equivalent experience).5+ years of Facilities Engineering, CAD Support, or Engineering Document Control experience.Experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.Strong knowledge of cGMP/FDA documentation requirements.Hands-on experience with CAD systems (Adept CAD preferred).Experience with EDMS/document control systems.Familiarity with CMMS systems, preferably Blue Mountain.Experience supporting Change Controls, CAPAs, Deviations, and Validation activities.Strong organizational, communication, and cross-functional collaboration skills.Preferred QualificationsExperience managing engineering drawings and As-Built documentation.Knowledge of facility utilities, maintenance systems, and spare parts management.Experience supporting regulatory inspections and maintaining audit-ready documentation.","company":"Lt Technology Services","rawCompany":"lt technology services","city":"Plainville","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-07-03T10:34:30.729Z","occupations":[{"code":"11-3013.00","title":"Facilities Managers","slug":"facilities-managers"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"},{"code":"17-3022.00","title":"Civil Engineering Technologists and Technicians","slug":"civil-engineering-technologists-and-technicians"}],"industries":[{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"236210","title":"Industrial Building Construction","slug":"industrial-building-construction"},{"code":"561210","title":"Facilities Support Services","slug":"facilities-support-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Facilities Engineer","description":"We are seeking an experienced Facilities Engineer – CAD Support to join a leading life sciences organization in Plainville, MA. This role will support Facilities Engineering by managing engineering documentation, CAD services, and the site's spare parts program while ensuring compliance with cGMP and quality standards.Key ResponsibilitiesManage and maintain GMP and Non-GMP engineering drawings and documentation.Serve as the primary liaison between Facilities Engineering, Project Management, Validation, and Quality teams.Maintain engineering documentation using the Adept Documentation System (EDMS).Update, revise, and manage engineering drawings utilizing the Adept CAD system.Develop and maintain procedures for engineering documentation and periodic drawing reviews.Manage the site's spare parts program, including inventory planning and risk assessments for critical facility, utility, and process equipment.Support Change Controls, CAPAs, Deviations, and engineering documentation updates.Maintain CMMS work orders and engineering drawing records (Blue Mountain preferred).Ensure engineering documentation is audit-ready and supports internal and regulatory inspections.Oversee contractor documentation activities to ensure compliance with site standards.Required QualificationsBachelor's degree in Engineering or a related technical discipline (or equivalent experience).5+ years of Facilities Engineering, CAD Support, or Engineering Document Control experience.Experience in pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments.Strong knowledge of cGMP/FDA documentation requirements.Hands-on experience with CAD systems (Adept CAD preferred).Experience with EDMS/document control systems.Familiarity with CMMS systems, preferably Blue Mountain.Experience supporting Change Controls, CAPAs, Deviations, and Validation activities.Strong organizational, communication, and cross-functional collaboration skills.Preferred QualificationsExperience managing engineering drawings and As-Built documentation.Knowledge of facility utilities, maintenance systems, and spare parts management.Experience supporting regulatory inspections and maintaining audit-ready documentation.","datePosted":"2026-07-03T10:34:30.729Z","dateModified":"2026-07-03T10:34:30.729Z","hiringOrganization":{"@type":"Organization","name":"Lt Technology Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Plainville","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"7db1aa0d77fa8a496c6250f6"},"url":"https://jobsearcher.com/jobs/7db1aa0d77fa8a496c6250f6"}}