{"schemaVersion":"jobsearcher.job.v1","id":"e1d4984968eba52f2e08fb72","url":"https://jobsearcher.com/jobs/e1d4984968eba52f2e08fb72","canonicalUrl":"https://jobsearcher.com/jobs/e1d4984968eba52f2e08fb72","title":"Product Development Engineer 2","description":"Acumed LLC\n\nAs a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway—you’ll be doing things that matter, leading at every level, and winning a better way. We’re committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone’s empowered to be their best.\n\nLocation\nHillsboro, Oregon\n\nJob Scope\nThe Product Development Engineer 2 supports the development of medical devices from concept to commercialization, including research, planning, concept development, specification generation, testing, validation, and communication with cross‑functional teams, management, and customers.\n\nDuties / Responsibilities\n\nDevelop implant and instrument designs using CAD models, drawings, and GD&T based on clinical research and collaboration with cross‑functional teams and clinical experts.\n\nLead engineering deliverables for small projects or portions of larger projects within Product Development Teams (PDTs) from concept through product launch and sustaining transfer.\n\nCommunicate technical concepts effectively with internal teams, vendors, sales teams, and healthcare professionals.\n\nSupport design control and risk management activities including traceability matrices, design verification and validation, design reviews, and associated testing.\n\nEvaluate designs through engineering analysis and testing including mechanical testing, cadaver labs, FEA, root cause analysis, tolerance stack analysis, and statistical tools.\n\nReview CAD models and drawings for tolerancing and manufacturability and contribute to Best Known Methods (BKMs) and quality checks.\n\nSupport engineering change management activities including drawing approvals and Engineering Change Orders within PLM systems (e.g., Windchill, SAP).\n\nResearch intellectual property landscapes and contribute to generation of new intellectual property.\n\nDevelop expertise in assigned technical specialty areas and apply anatomical knowledge to product development projects.\n\nSupport literature research, competitive analysis, and occasional customer‑facing events.\n\nQualifications\n\nBachelor’s degree in Mechanical Engineering, Bio‑Mechanical Engineering, or equivalent with 2+ years’ experience preferred; or 8 years of medical device development experience.\n\nAbility to communicate clearly and effectively with teammates and managers.\n\nAbility to lead PDTs on small projects.\n\nExperience writing test protocols and reports and conducting testing with limited supervision.\n\nApplied knowledge of 3D/2D CAD modeling and drawings for implants or instruments.\n\nKnowledge of Level 1 & 2 GD&T principles.\n\nBasic FEA analysis knowledge to mitigate design risks.\n\nExperience managing ECOs through completion.\n\nKnowledge of root cause analysis techniques.\n\nAbility to review medical literature, summarize clinical data, and write reports.\n\nAbility to review patents and understand intellectual property considerations.\n\nFamiliarity with design control processes in regulated environments.\n\nUnderstanding of anatomy and clinical indications for assigned projects.\n\nAbility to conduct literature searches and develop competitive product analyses.\n\nFollowing receipt of a conditional offer of employment, candidates will be required to complete additional job‑related screening processes as permitted or required by applicable law.\n\nWe are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to careers@marmon.com , and please be sure to include the title and the location of the position for which you are applying.\n\n#J-18808-Ljbffr","company":"SupportFinity","rawCompany":"supportfinity","city":"Hillsboro","state":"IL","isRemote":false,"isActive":false,"createdAt":"2026-06-20T04:20:51.617Z","occupations":[{"code":"17-2031.00","title":"Bioengineers and Biomedical Engineers","slug":"bioengineers-and-biomedical-engineers"},{"code":"17-2141.00","title":"Mechanical Engineers","slug":"mechanical-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"}],"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":"Product Development Engineer 2","description":"Acumed LLC\n\nAs a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway—you’ll be doing things that matter, leading at every level, and winning a better way. We’re committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone’s empowered to be their best.\n\nLocation\nHillsboro, Oregon\n\nJob Scope\nThe Product Development Engineer 2 supports the development of medical devices from concept to commercialization, including research, planning, concept development, specification generation, testing, validation, and communication with cross‑functional teams, management, and customers.\n\nDuties / Responsibilities\n\nDevelop implant and instrument designs using CAD models, drawings, and GD&T based on clinical research and collaboration with cross‑functional teams and clinical experts.\n\nLead engineering deliverables for small projects or portions of larger projects within Product Development Teams (PDTs) from concept through product launch and sustaining transfer.\n\nCommunicate technical concepts effectively with internal teams, vendors, sales teams, and healthcare professionals.\n\nSupport design control and risk management activities including traceability matrices, design verification and validation, design reviews, and associated testing.\n\nEvaluate designs through engineering analysis and testing including mechanical testing, cadaver labs, FEA, root cause analysis, tolerance stack analysis, and statistical tools.\n\nReview CAD models and drawings for tolerancing and manufacturability and contribute to Best Known Methods (BKMs) and quality checks.\n\nSupport engineering change management activities including drawing approvals and Engineering Change Orders within PLM systems (e.g., Windchill, SAP).\n\nResearch intellectual property landscapes and contribute to generation of new intellectual property.\n\nDevelop expertise in assigned technical specialty areas and apply anatomical knowledge to product development projects.\n\nSupport literature research, competitive analysis, and occasional customer‑facing events.\n\nQualifications\n\nBachelor’s degree in Mechanical Engineering, Bio‑Mechanical Engineering, or equivalent with 2+ years’ experience preferred; or 8 years of medical device development experience.\n\nAbility to communicate clearly and effectively with teammates and managers.\n\nAbility to lead PDTs on small projects.\n\nExperience writing test protocols and reports and conducting testing with limited supervision.\n\nApplied knowledge of 3D/2D CAD modeling and drawings for implants or instruments.\n\nKnowledge of Level 1 & 2 GD&T principles.\n\nBasic FEA analysis knowledge to mitigate design risks.\n\nExperience managing ECOs through completion.\n\nKnowledge of root cause analysis techniques.\n\nAbility to review medical literature, summarize clinical data, and write reports.\n\nAbility to review patents and understand intellectual property considerations.\n\nFamiliarity with design control processes in regulated environments.\n\nUnderstanding of anatomy and clinical indications for assigned projects.\n\nAbility to conduct literature searches and develop competitive product analyses.\n\nFollowing receipt of a conditional offer of employment, candidates will be required to complete additional job‑related screening processes as permitted or required by applicable law.\n\nWe are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to careers@marmon.com , and please be sure to include the title and the location of the position for which you are applying.\n\n#J-18808-Ljbffr","datePosted":"2026-06-20T04:20:51.617Z","dateModified":"2026-06-20T04:20:51.617Z","hiringOrganization":{"@type":"Organization","name":"SupportFinity","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Hillsboro","addressRegion":"IL","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e1d4984968eba52f2e08fb72"},"url":"https://jobsearcher.com/jobs/e1d4984968eba52f2e08fb72"}}