{"schemaVersion":"jobsearcher.job.v1","id":"6f331cba988d334bed6da2e7","url":"https://jobsearcher.com/jobs/6f331cba988d334bed6da2e7","canonicalUrl":"https://jobsearcher.com/jobs/6f331cba988d334bed6da2e7","title":"Engineer III","description":"Roles & Responsibilities\n\nThe Combination and Medical Device Products Consumable Device US team is expanding its support for on‑market devices.\n\nThis role will be responsible for on‑market change execution, product lifecycle management, and manufacturing support specific to the product design.\n\nProficiency with medical device/pharmaceutical DHF traceability is required.\n\nProficiency with test execution, deviation reporting and management, data review, and report writing is required.\n\nExperience with medical device EU and/or FDA regulations is required.\n\nIn addition to product support, you will also be responsible for standardizing and simplifying activities within the team to enable more efficient development and marketed product support.\n\nEducation & Experience\n\nBachelor of Science degree with 3+ years of experience in medical device or pharmaceutical development roles.\n\nGraduate degree in a technical or scientific field. Prior experience in consumable medical device/pharmaceutical development.\n\nMedical device/pharmaceutical development, office, and laboratory settings.\n\nDesign History File product lifecycle management experience.\n\nEngineering degree in bioengineering, chemical engineering, or mechanical engineering.\n\nOn‑market supplier changes.\n\nKnowledge of applicable global regulatory requirements and industry standards (MDR requirements, ISO 13485, ISO 14971, ISO 10993, etc.).\n\nExceptional written and verbal communication skills, and the ability to clearly articulate development challenges and implementation strategies to stakeholders across a broad range of functional groups at all levels of the organization, including external vendors.\n\n#J-18808-Ljbffr","company":"Creative Solutions Services","rawCompany":"creative solutions services","city":"Chicago","state":"IL","isRemote":false,"isActive":true,"createdAt":"2026-07-09T03:19:30.639Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2031.00","title":"Bioengineers and Biomedical Engineers","slug":"bioengineers-and-biomedical-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":"Engineer III","description":"Roles & Responsibilities\n\nThe Combination and Medical Device Products Consumable Device US team is expanding its support for on‑market devices.\n\nThis role will be responsible for on‑market change execution, product lifecycle management, and manufacturing support specific to the product design.\n\nProficiency with medical device/pharmaceutical DHF traceability is required.\n\nProficiency with test execution, deviation reporting and management, data review, and report writing is required.\n\nExperience with medical device EU and/or FDA regulations is required.\n\nIn addition to product support, you will also be responsible for standardizing and simplifying activities within the team to enable more efficient development and marketed product support.\n\nEducation & Experience\n\nBachelor of Science degree with 3+ years of experience in medical device or pharmaceutical development roles.\n\nGraduate degree in a technical or scientific field. Prior experience in consumable medical device/pharmaceutical development.\n\nMedical device/pharmaceutical development, office, and laboratory settings.\n\nDesign History File product lifecycle management experience.\n\nEngineering degree in bioengineering, chemical engineering, or mechanical engineering.\n\nOn‑market supplier changes.\n\nKnowledge of applicable global regulatory requirements and industry standards (MDR requirements, ISO 13485, ISO 14971, ISO 10993, etc.).\n\nExceptional written and verbal communication skills, and the ability to clearly articulate development challenges and implementation strategies to stakeholders across a broad range of functional groups at all levels of the organization, including external vendors.\n\n#J-18808-Ljbffr","datePosted":"2026-07-09T03:19:30.639Z","dateModified":"2026-07-09T03:19:30.639Z","hiringOrganization":{"@type":"Organization","name":"Creative Solutions Services","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Chicago","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"6f331cba988d334bed6da2e7"},"url":"https://jobsearcher.com/jobs/6f331cba988d334bed6da2e7"}}