{"schemaVersion":"jobsearcher.job.v1","id":"b4d863f674752f65b1dcfc15","url":"https://jobsearcher.com/jobs/b4d863f674752f65b1dcfc15","canonicalUrl":"https://jobsearcher.com/jobs/b4d863f674752f65b1dcfc15","title":"Process Engineer","description":"Roles & Responsibilities\n\nWrite and execute validation protocols and reports (IQ, OQ, PQ).\n\nDevelop and implement manufacturing processes, specifications, operator instructions, process studies, and production readiness activities.\n\nConduct investigations, root cause analysis, problem solving, and prepare reports/presentations.\n\nUpdate procedures, manufacturing specifications, bills, routes, and travelers for product/process changes in PLM systems.\n\nWork with equipment manufacturers and distributors to develop user requirements.\n\nPartner with Operations, OpEx, Planning, Engineering, and Quality teams to align validation strategy, author documents, coordinate execution, and manage approvals.\n\nEnsure adherence to FDA regulations, regulatory requirements, company policies, and operating procedures.\n\nIdentify opportunities for process improvement and implement best practices.\n\nMaintain positive and cooperative communication with employees, customers, contractors, and vendors.\n\nBackground in medical device or other regulated industries.\n\nExperience with machining, metal finishing, laser processing, or production automation.\n\nPractical exposure to machining, casting, finishing, laser processing, or automation.\n\nKnowledge of statistical data analysis tools (e.g., Minitab).\n\nBasic understanding of Geometric Dimensioning and Tolerancing.\n\nWillingness to support global projects, including travel.\n\nRequirements\n\n2-4 years of experience in manufacturing and/or process engineering.\n\nStrong technical writing skills with awareness of intended audience.\n\nAbility to effectively communicate with operators, peers, and management in both written and oral formats.\n\nHands-on experience with validation protocols.\n\nExperience in medical device and/or regulated manufacturing environment.\nInterpersonal Skills:\nPersuasive communication and strong interpersonal abilities.\nProficiency with Microsoft Office tools.\n\n#J-18808-Ljbffr","company":"Creative Solutions Services","rawCompany":"creative solutions services","city":"Raynham","state":"MA","isRemote":false,"isActive":true,"createdAt":"2026-06-17T03:38:18.194Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"}],"industries":[{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"333248","title":"All Other Industrial Machinery Manufacturing","slug":"all-other-industrial-machinery-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer","description":"Roles & Responsibilities\n\nWrite and execute validation protocols and reports (IQ, OQ, PQ).\n\nDevelop and implement manufacturing processes, specifications, operator instructions, process studies, and production readiness activities.\n\nConduct investigations, root cause analysis, problem solving, and prepare reports/presentations.\n\nUpdate procedures, manufacturing specifications, bills, routes, and travelers for product/process changes in PLM systems.\n\nWork with equipment manufacturers and distributors to develop user requirements.\n\nPartner with Operations, OpEx, Planning, Engineering, and Quality teams to align validation strategy, author documents, coordinate execution, and manage approvals.\n\nEnsure adherence to FDA regulations, regulatory requirements, company policies, and operating procedures.\n\nIdentify opportunities for process improvement and implement best practices.\n\nMaintain positive and cooperative communication with employees, customers, contractors, and vendors.\n\nBackground in medical device or other regulated industries.\n\nExperience with machining, metal finishing, laser processing, or production automation.\n\nPractical exposure to machining, casting, finishing, laser processing, or automation.\n\nKnowledge of statistical data analysis tools (e.g., Minitab).\n\nBasic understanding of Geometric Dimensioning and Tolerancing.\n\nWillingness to support global projects, including travel.\n\nRequirements\n\n2-4 years of experience in manufacturing and/or process engineering.\n\nStrong technical writing skills with awareness of intended audience.\n\nAbility to effectively communicate with operators, peers, and management in both written and oral formats.\n\nHands-on experience with validation protocols.\n\nExperience in medical device and/or regulated manufacturing environment.\nInterpersonal Skills:\nPersuasive communication and strong interpersonal abilities.\nProficiency with Microsoft Office tools.\n\n#J-18808-Ljbffr","datePosted":"2026-06-17T03:38:18.194Z","dateModified":"2026-06-17T03:38:18.194Z","hiringOrganization":{"@type":"Organization","name":"Creative Solutions Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Raynham","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"b4d863f674752f65b1dcfc15"},"url":"https://jobsearcher.com/jobs/b4d863f674752f65b1dcfc15"}}