{"schemaVersion":"jobsearcher.job.v1","id":"724f6be17c8e192b0e7704ee","url":"https://jobsearcher.com/jobs/724f6be17c8e192b0e7704ee","canonicalUrl":"https://jobsearcher.com/jobs/724f6be17c8e192b0e7704ee","title":"Process Engineer III","description":"Overview\nWe are seeking a highly motivated and experienced Process Engineer III to lead multi-product project execution, manufacturing support, and technology transfer efforts at our Rancho Dominguez facility. This role provides technical leadership at the site level while collaborating closely with our global engineering network to deliver strategic initiatives.\n\nThe ideal candidate has a strong background in manufacturing, with expertise in process engineering, equipment qualification, and preferably within GMP or ISO 9001 environments. Success in this role requires technical proficiency, a collaborative mindset, and the ability to drive projects with minimal oversight.\nResponsibilities\nAct as a Subject Matter Expert for Tangential Flow Filtration (TFF) and other bioprocessing manufacturing systems.\nLead projects in equipment design, tech transfer, process validation, and facility upgrades.\nConceives, plans, and executes projects or aspects of projects related to the strategic needs of the company.\nPartner with global engineering teams to support corporate initiatives and site expansion.\nIdentify and implement process improvements, ensuring compliance with industry standards and regulations.\nDevelop and maintain engineering documentation including test protocols, change controls, and technical reports.\nGuide the integration of new products and manufacturing processes, supporting early-phase development through commercialization.\nMentor junior team members and support standardization and training of best practices.\nApply statistical tools to support validation and process optimization efforts.\nDrive innovation in filtration systems and related support infrastructure to enhance performance and scalability.\nQualifications\nEducation and/or Work Experience:\n\nBachelor’s degree in Engineering required.\n5-7 years of experience in medical devices, aerospace, pharmaceuticals, or biologics manufacturing.\nHands-on experience with:\nProcess validation and equipment qualification\nSolidWorks/CAD, MS Office, and electronic file management systems.\nTech transfer between sites\nData analysis and automation\nFiltration systems (Tangential Flow Filtration (TFF), Hollow Fiber, Flat Sheet Membranes)\nStrong knowledge of ISO 9001 and GMP manufacturing standards.\nFamiliarity with single-use systems, sterilization techniques, and lean manufacturing principles preferred.\nDemonstrated ability to lead cross-functional teams and manage projects in a matrixed organization.\nHigh level of personal integrity, adaptability, and leadership by example.\n\nOther requirements:\n\nCapable of independently defining and executing projects.\nProvides technical direction and feedback to teams across disciplines.\nBalances day-to-day plant support (40%) with project execution (60%).\nCommunicates clearly with senior leadership on project scope, risks, and progress.\nDelegates tasks effectively and contributes to team development.\n\nPhysical Requirements:\n\nRegular work in cleanroom and laboratory environments.\nExposure to chemicals, mechanical systems, and occasional electrical hazards.\nMay be required to lift up to 50 lbs and operate in areas with noise and vibration.","company":"Repligen","rawCompany":"repligen","city":"Compton","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-04-12T21:28:50.491Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"333248","title":"All Other Industrial Machinery Manufacturing","slug":"all-other-industrial-machinery-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer III","description":"Overview\nWe are seeking a highly motivated and experienced Process Engineer III to lead multi-product project execution, manufacturing support, and technology transfer efforts at our Rancho Dominguez facility. This role provides technical leadership at the site level while collaborating closely with our global engineering network to deliver strategic initiatives.\n\nThe ideal candidate has a strong background in manufacturing, with expertise in process engineering, equipment qualification, and preferably within GMP or ISO 9001 environments. Success in this role requires technical proficiency, a collaborative mindset, and the ability to drive projects with minimal oversight.\nResponsibilities\nAct as a Subject Matter Expert for Tangential Flow Filtration (TFF) and other bioprocessing manufacturing systems.\nLead projects in equipment design, tech transfer, process validation, and facility upgrades.\nConceives, plans, and executes projects or aspects of projects related to the strategic needs of the company.\nPartner with global engineering teams to support corporate initiatives and site expansion.\nIdentify and implement process improvements, ensuring compliance with industry standards and regulations.\nDevelop and maintain engineering documentation including test protocols, change controls, and technical reports.\nGuide the integration of new products and manufacturing processes, supporting early-phase development through commercialization.\nMentor junior team members and support standardization and training of best practices.\nApply statistical tools to support validation and process optimization efforts.\nDrive innovation in filtration systems and related support infrastructure to enhance performance and scalability.\nQualifications\nEducation and/or Work Experience:\n\nBachelor’s degree in Engineering required.\n5-7 years of experience in medical devices, aerospace, pharmaceuticals, or biologics manufacturing.\nHands-on experience with:\nProcess validation and equipment qualification\nSolidWorks/CAD, MS Office, and electronic file management systems.\nTech transfer between sites\nData analysis and automation\nFiltration systems (Tangential Flow Filtration (TFF), Hollow Fiber, Flat Sheet Membranes)\nStrong knowledge of ISO 9001 and GMP manufacturing standards.\nFamiliarity with single-use systems, sterilization techniques, and lean manufacturing principles preferred.\nDemonstrated ability to lead cross-functional teams and manage projects in a matrixed organization.\nHigh level of personal integrity, adaptability, and leadership by example.\n\nOther requirements:\n\nCapable of independently defining and executing projects.\nProvides technical direction and feedback to teams across disciplines.\nBalances day-to-day plant support (40%) with project execution (60%).\nCommunicates clearly with senior leadership on project scope, risks, and progress.\nDelegates tasks effectively and contributes to team development.\n\nPhysical Requirements:\n\nRegular work in cleanroom and laboratory environments.\nExposure to chemicals, mechanical systems, and occasional electrical hazards.\nMay be required to lift up to 50 lbs and operate in areas with noise and vibration.","datePosted":"2026-04-12T21:28:50.491Z","dateModified":"2026-04-12T21:28:50.491Z","hiringOrganization":{"@type":"Organization","name":"Repligen","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Compton","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"724f6be17c8e192b0e7704ee"},"url":"https://jobsearcher.com/jobs/724f6be17c8e192b0e7704ee"}}