{"schemaVersion":"jobsearcher.job.v1","id":"84593dbb60f661c19363dfd8","url":"https://jobsearcher.com/jobs/84593dbb60f661c19363dfd8","canonicalUrl":"https://jobsearcher.com/jobs/84593dbb60f661c19363dfd8","title":"Sr Manufacturing Engineer","description":"Sr Manufacturing Engineer Location: San Francisco, CA (Onsite – 5 days a week)\nDuration: 6+ months contract\nIRC: IRC289521\nMedical device experience is mandatory.\nJob Description Desired Qualifications:\nSolidWorks or similar 3D modeling and design experience.\nProject leadership/management experience and/or leading a team.\nKnowledge of Lean and Six Sigma concepts and root cause problem solving.\nAbout You:\nBachelor’s Degree in Engineering or a related field required; Master’s degree preferred.\nMust have at least 5+ years of related experience in the medical device or similar field.\nExperience with Continuous Process Improvement and Process Validations within a medical device manufacturing environment.\nStrong creative and critical thinking skills.\nAbility to work in a fast-paced, cross-functional environment.\nSome travel may be required – must be able to travel within the US.\nExperience working in ISO 13485 and FDA regulated environments.\nJob Responsibilities Responsibilities include:\nSupport of new and existing manufacturing processes, new products, product changes and enhancements, as well as related tooling and fixtures.\nSupport prototype and pilot production, facilities, and planning, when appropriate.\nInterfaces with other departments to solve production problems.\nInvestigation and testing of product processes.\nLead manufacturing efforts associated with new product transfer between R&D and manufacturing.\nDrafts and executes validation of product, equipment, and processes.\nManages builds for new product development in prototype and pilot production setting, including training of operators and coordination with production planning as needed.\nAnalyze data and improve processes to assure robust/repeatable manufacturing processes.\nConfers with appropriate departments, resources, and/or outside services to prepare process modifications, clarify problems and develop processes.\nReview and/or develop manufacturing and engineering documents.\nProvide solutions to complex problems including, but not limited to, those related to process, equipment, material, supply chain, documentation, equipment validation, IQ/OQ/PQ, PLM, and other applicable QMS / business processes.\nPerform root cause analysis and implement process improvements to improve manufacturing yield.\nSupport the design and development of tooling and fixtures to effectively manufacture new and existing products.\nSearches and implements new technologies to improve manufacturing processes and equipment design.\nDemonstrated analytical skills with the ability to present data in meaningful and relevant fashion to aid in decision making process.\nEstablish and maintain data monitoring for key processes metrics in manufacturing.\nExcellent written and verbal communication skills.\n\n#J-18808-Ljbffr","company":"Highbrow","rawCompany":"highbrow","city":"Millbrae","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-06-26T05:32:00.704Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"},{"code":"11-3051.00","title":"Industrial Production Managers","slug":"industrial-production-managers"}],"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":"Sr Manufacturing Engineer","description":"Sr Manufacturing Engineer Location: San Francisco, CA (Onsite – 5 days a week)\nDuration: 6+ months contract\nIRC: IRC289521\nMedical device experience is mandatory.\nJob Description Desired Qualifications:\nSolidWorks or similar 3D modeling and design experience.\nProject leadership/management experience and/or leading a team.\nKnowledge of Lean and Six Sigma concepts and root cause problem solving.\nAbout You:\nBachelor’s Degree in Engineering or a related field required; Master’s degree preferred.\nMust have at least 5+ years of related experience in the medical device or similar field.\nExperience with Continuous Process Improvement and Process Validations within a medical device manufacturing environment.\nStrong creative and critical thinking skills.\nAbility to work in a fast-paced, cross-functional environment.\nSome travel may be required – must be able to travel within the US.\nExperience working in ISO 13485 and FDA regulated environments.\nJob Responsibilities Responsibilities include:\nSupport of new and existing manufacturing processes, new products, product changes and enhancements, as well as related tooling and fixtures.\nSupport prototype and pilot production, facilities, and planning, when appropriate.\nInterfaces with other departments to solve production problems.\nInvestigation and testing of product processes.\nLead manufacturing efforts associated with new product transfer between R&D and manufacturing.\nDrafts and executes validation of product, equipment, and processes.\nManages builds for new product development in prototype and pilot production setting, including training of operators and coordination with production planning as needed.\nAnalyze data and improve processes to assure robust/repeatable manufacturing processes.\nConfers with appropriate departments, resources, and/or outside services to prepare process modifications, clarify problems and develop processes.\nReview and/or develop manufacturing and engineering documents.\nProvide solutions to complex problems including, but not limited to, those related to process, equipment, material, supply chain, documentation, equipment validation, IQ/OQ/PQ, PLM, and other applicable QMS / business processes.\nPerform root cause analysis and implement process improvements to improve manufacturing yield.\nSupport the design and development of tooling and fixtures to effectively manufacture new and existing products.\nSearches and implements new technologies to improve manufacturing processes and equipment design.\nDemonstrated analytical skills with the ability to present data in meaningful and relevant fashion to aid in decision making process.\nEstablish and maintain data monitoring for key processes metrics in manufacturing.\nExcellent written and verbal communication skills.\n\n#J-18808-Ljbffr","datePosted":"2026-06-26T05:32:00.704Z","dateModified":"2026-06-26T05:32:00.704Z","hiringOrganization":{"@type":"Organization","name":"Highbrow","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Millbrae","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"84593dbb60f661c19363dfd8"},"url":"https://jobsearcher.com/jobs/84593dbb60f661c19363dfd8"}}