{"schemaVersion":"jobsearcher.job.v1","id":"2504739abdf1c0cf096e518e","url":"https://jobsearcher.com/jobs/2504739abdf1c0cf096e518e","canonicalUrl":"https://jobsearcher.com/jobs/2504739abdf1c0cf096e518e","title":"Process Engineer","description":"Primary Responsibilities would include, but is not limited to:\nAuthor study protocols and technical reports, and revise process documents as needed to support technology transfer and process changes.\nPerform and support data monitoring of manufacturing processes to understand process capability.\nSupport production related investigations, ensuring compliance with internal standards and regulatory requirements.\nReview executed batch records to ensure process is operating within the validated state.\nUnderstand and manage tools and templates that can be used to quantify impact and criticality for parameters and attributes within Client and/or CMO unit operations.\nEnsure manufacturing processes are in a state of control, harmonized across the cell therapy network.\nSupport continuous improvement for technical and business processes.\nLeverage and maintain professional relationships with external partners.\nDesired Background and Experience B.S. or M.S with 4-7 years of relevant experience in Biochemical, Chemical, or Biomedical Engineering or Cell Biology/Immunology discipline (PhD overqualified).\nExperience with cellular therapies is highly preferred.\n4+ years of MS office, experience with JMP is preferred.\n4+ years' experience in a regulated manufacturing environment is highly preferred.\n1+ years of experience in technical writing or deviation writing.\nFlexibility to work across East Coast and West Coast time zones.\nExcellent communication, writing, organizational, teamwork, and presentation skills.\nExceptional interpersonal skills to work with teams in different functions and organizations.\n\n#J-18808-Ljbffr","company":"TechDigital Group","rawCompany":"techdigital group","city":"Seattle","state":"WA","isRemote":false,"isActive":false,"createdAt":"2026-09-10T03:17:26.188Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2041.00","title":"Chemical Engineers","slug":"chemical-engineers"}],"industries":[{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer","description":"Primary Responsibilities would include, but is not limited to:\nAuthor study protocols and technical reports, and revise process documents as needed to support technology transfer and process changes.\nPerform and support data monitoring of manufacturing processes to understand process capability.\nSupport production related investigations, ensuring compliance with internal standards and regulatory requirements.\nReview executed batch records to ensure process is operating within the validated state.\nUnderstand and manage tools and templates that can be used to quantify impact and criticality for parameters and attributes within Client and/or CMO unit operations.\nEnsure manufacturing processes are in a state of control, harmonized across the cell therapy network.\nSupport continuous improvement for technical and business processes.\nLeverage and maintain professional relationships with external partners.\nDesired Background and Experience B.S. or M.S with 4-7 years of relevant experience in Biochemical, Chemical, or Biomedical Engineering or Cell Biology/Immunology discipline (PhD overqualified).\nExperience with cellular therapies is highly preferred.\n4+ years of MS office, experience with JMP is preferred.\n4+ years' experience in a regulated manufacturing environment is highly preferred.\n1+ years of experience in technical writing or deviation writing.\nFlexibility to work across East Coast and West Coast time zones.\nExcellent communication, writing, organizational, teamwork, and presentation skills.\nExceptional interpersonal skills to work with teams in different functions and organizations.\n\n#J-18808-Ljbffr","datePosted":"2026-09-10T03:17:26.188Z","dateModified":"2026-09-10T03:17:26.188Z","hiringOrganization":{"@type":"Organization","name":"TechDigital 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