{"schemaVersion":"jobsearcher.job.v1","id":"3f97ffe424bc6bdd5cebd2d4","url":"https://jobsearcher.com/jobs/3f97ffe424bc6bdd5cebd2d4","canonicalUrl":"https://jobsearcher.com/jobs/3f97ffe424bc6bdd5cebd2d4","title":"Manufacturing Engineer","description":"Job Description\nThe Manufacturing Engineer will provide engineering support for the operational issues pertaining to the production of a full line of surgical positioning products, in a Class 1 FDA regulated environment.\n\nUse mechanical engineering skills to develop solutions for assembly and design problems and to support New Product Development, Purchasing and external vendors. Develop and maintain effective and economical manufacturing processes. Responsible for work instructions, regulatory compliance, processing engineering changes, troubleshooting problems, and supporting changes in production methods.\n\nResponsible for total product quality, which includes resolving quality problems, certifying processes, and implementing process control.\n\nInitiate, Prepare and Complete Engineering Change Orders.\n\nConduct and document engineering investigations and tests.\n\nRevise and prepare Engineering Documentation - Drawings, 3D Models, Test Protocols, BOM's, etc.\n\nParticipate in activities related to NCMR, inspection and complaint evaluation.\n\nParticipate in Cost Reduction Activities and product redesigns.\n\nParticipate in NPD teams and Cost teams to ensure DFMA of products, review drawings, work instructions, BOM's and other engineering documents and successful transfer products to manufacturing through validation testing.\n\nQualifications:\n\n2+ years of experience working in a medical product environment is preferred.\n\nDegree in Mechanical or Manufacturing Engineering.\n\nInnate mechanical engineering skills and hands on mechanical aptitude.\n\nComputer experience in Windows, Microsoft Office; Excel, Word, PowerPoint and Outlook.\n\nStrong organizational, communication and written skills.\n\nSelf-motivated/Self-driven, enthusiastic, cooperative, and positive behavior.\n\nProficient with SolidWorks or another CAD software program.\n\nAdditional Information\nAll your information will be kept confidential according to EEO guidelines.\n\n#J-18808-Ljbffr","company":"Makro Technologies","rawCompany":"makro technologies","city":"Acton","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-07-16T03:44:53.957Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"},{"code":"17-2141.00","title":"Mechanical Engineers","slug":"mechanical-engineers"}],"industries":[{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Manufacturing Engineer","description":"Job Description\nThe Manufacturing Engineer will provide engineering support for the operational issues pertaining to the production of a full line of surgical positioning products, in a Class 1 FDA regulated environment.\n\nUse mechanical engineering skills to develop solutions for assembly and design problems and to support New Product Development, Purchasing and external vendors. Develop and maintain effective and economical manufacturing processes. Responsible for work instructions, regulatory compliance, processing engineering changes, troubleshooting problems, and supporting changes in production methods.\n\nResponsible for total product quality, which includes resolving quality problems, certifying processes, and implementing process control.\n\nInitiate, Prepare and Complete Engineering Change Orders.\n\nConduct and document engineering investigations and tests.\n\nRevise and prepare Engineering Documentation - Drawings, 3D Models, Test Protocols, BOM's, etc.\n\nParticipate in activities related to NCMR, inspection and complaint evaluation.\n\nParticipate in Cost Reduction Activities and product redesigns.\n\nParticipate in NPD teams and Cost teams to ensure DFMA of products, review drawings, work instructions, BOM's and other engineering documents and successful transfer products to manufacturing through validation testing.\n\nQualifications:\n\n2+ years of experience working in a medical product environment is preferred.\n\nDegree in Mechanical or Manufacturing Engineering.\n\nInnate mechanical engineering skills and hands on mechanical aptitude.\n\nComputer experience in Windows, Microsoft Office; Excel, Word, PowerPoint and Outlook.\n\nStrong organizational, communication and written skills.\n\nSelf-motivated/Self-driven, enthusiastic, cooperative, and positive behavior.\n\nProficient with SolidWorks or another CAD software program.\n\nAdditional Information\nAll your information will be kept confidential according to EEO guidelines.\n\n#J-18808-Ljbffr","datePosted":"2026-07-16T03:44:53.957Z","dateModified":"2026-07-16T03:44:53.957Z","hiringOrganization":{"@type":"Organization","name":"Makro Technologies","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Acton","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"3f97ffe424bc6bdd5cebd2d4"},"url":"https://jobsearcher.com/jobs/3f97ffe424bc6bdd5cebd2d4"}}