{"schemaVersion":"jobsearcher.job.v1","id":"e76e9c1b64eb5d6a4e4002fc","url":"https://jobsearcher.com/jobs/e76e9c1b64eb5d6a4e4002fc","canonicalUrl":"https://jobsearcher.com/jobs/e76e9c1b64eb5d6a4e4002fc","title":"Manufacturing Process Developer","description":"Job Summary\n5+ years of Medical device Manufacturing experience\nSupport in Manufacturing process remediation and readiness activities for new product launch.\nSupport Design Transfer deliverables, including tracking and scheduling.\nSupport/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.\nRisk Management updates – PFMEA.\nPart creation in Windchill. BOM and configuration management.\nWork with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\n\nPreferred\n\nKnowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.\nPrevious medical device experience\nKey Responsibilities\n5+ years of Medical device Manufacturing experience\nSupport in Manufacturing process remediation and readiness activities for new product launch.\nSupport Design Transfer deliverables, including tracking and scheduling.\nSupport/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.\nRisk Management updates – PFMEA.\nPart creation in Windchill. BOM and configuration management.\nWork with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\n\nPreferred\n\nKnowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.\nPrevious medical device experience\nSkill Requirements\n5+ years of Medical device Manufacturing experience\nSupport in Manufacturing process remediation and readiness activities for new product launch.\nSupport Design Transfer deliverables, including tracking and scheduling.\nSupport/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.\nRisk Management updates – PFMEA.\nPart creation in Windchill. BOM and configuration management.\nWork with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\n\nPreferred\n\nKnowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.\nPrevious medical device experience\nMust Have Skill\nManufacturing Processes,Process Validation\nGood to Have Skill\nOther Requirements\n5+ years of Medical device Manufacturing experience\nSupport in Manufacturing process remediation and readiness activities for new product launch.\nSupport Design Transfer deliverables, including tracking and scheduling.\nSupport/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.\nRisk Management updates – PFMEA.\nPart creation in Windchill. BOM and configuration management.\nWork with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\n\nPreferred\n\nKnowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.\nPrevious medical device experience","company":"Hcltech2","rawCompany":"hcltech2","city":"California City","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-11-07T10:02:51.580Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"}],"industries":[{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Manufacturing Process Developer","description":"Job Summary\n5+ years of Medical device Manufacturing experience\nSupport in Manufacturing process remediation and readiness activities for new product launch.\nSupport Design Transfer deliverables, including tracking and scheduling.\nSupport/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.\nRisk Management updates – PFMEA.\nPart creation in Windchill. BOM and configuration management.\nWork with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\n\nPreferred\n\nKnowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.\nPrevious medical device experience\nKey Responsibilities\n5+ years of Medical device Manufacturing experience\nSupport in Manufacturing process remediation and readiness activities for new product launch.\nSupport Design Transfer deliverables, including tracking and scheduling.\nSupport/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.\nRisk Management updates – PFMEA.\nPart creation in Windchill. BOM and configuration management.\nWork with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\n\nPreferred\n\nKnowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.\nPrevious medical device experience\nSkill Requirements\n5+ years of Medical device Manufacturing experience\nSupport in Manufacturing process remediation and readiness activities for new product launch.\nSupport Design Transfer deliverables, including tracking and scheduling.\nSupport/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.\nRisk Management updates – PFMEA.\nPart creation in Windchill. BOM and configuration management.\nWork with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\n\nPreferred\n\nKnowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.\nPrevious medical device experience\nMust Have Skill\nManufacturing Processes,Process Validation\nGood to Have Skill\nOther Requirements\n5+ years of Medical device Manufacturing experience\nSupport in Manufacturing process remediation and readiness activities for new product launch.\nSupport Design Transfer deliverables, including tracking and scheduling.\nSupport/Initiate Change Order for manufacturing documentation such as but not limited to, manufacturing procedures, shop floor paperwork, and inspection procedures.\nRisk Management updates – PFMEA.\nPart creation in Windchill. BOM and configuration management.\nWork with cross functional teams as required, especially with R&D, Quality, and Regulatory teams.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\n\nPreferred\n\nKnowledge of ISO and/or FDA quality system regulations as it pertains to design transfer and process control.\nPrevious medical device experience","datePosted":"2026-11-07T10:02:51.580Z","dateModified":"2026-11-07T10:02:51.580Z","hiringOrganization":{"@type":"Organization","name":"Hcltech2","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"California City","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"e76e9c1b64eb5d6a4e4002fc"},"url":"https://jobsearcher.com/jobs/e76e9c1b64eb5d6a4e4002fc"}}