{"schemaVersion":"jobsearcher.job.v1","id":"28a9f6866ef94f20c0259c1e","url":"https://jobsearcher.com/jobs/28a9f6866ef94f20c0259c1e","canonicalUrl":"https://jobsearcher.com/jobs/28a9f6866ef94f20c0259c1e","title":"Sterilization Process Engineer","description":"Seeking a Sterilization Process Engineer to lead iHP/VHP sterilization system validation and process implementation in a GMP-regulated medical device environment. Role includes cycle design, equipment qualification, enzymatic indicator (EI) validation, and compliance with FDA/ISO standards.\n\nKey Requirements\n\nBachelor’s in Engineering, Microbiology, or related field\n\n5+ years in sterilization/process validation under GMP\n\nHands‑on with iHP/VHP sterilization & EI monitoring\n\nKnowledge of GMP, ISO 13485, 21 CFR Part 820\n\nStrong technical writing & validation documentation skills\n\n#J-18808-Ljbffr","company":"S4 Analytics","rawCompany":"s4 analytics","city":"Florida","state":"NY","isRemote":false,"isActive":true,"createdAt":"2026-06-17T03:31:31.394Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"31-9093.00","title":"Medical Equipment Preparers","slug":"medical-equipment-preparers"},{"code":"17-2031.00","title":"Bioengineers and Biomedical Engineers","slug":"bioengineers-and-biomedical-engineers"}],"industries":[{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Sterilization Process Engineer","description":"Seeking a Sterilization Process Engineer to lead iHP/VHP sterilization system validation and process implementation in a GMP-regulated medical device environment. Role includes cycle design, equipment qualification, enzymatic indicator (EI) validation, and compliance with FDA/ISO standards.\n\nKey Requirements\n\nBachelor’s in Engineering, Microbiology, or related field\n\n5+ years in sterilization/process validation under GMP\n\nHands‑on with iHP/VHP sterilization & EI monitoring\n\nKnowledge of GMP, ISO 13485, 21 CFR Part 820\n\nStrong technical writing & validation documentation skills\n\n#J-18808-Ljbffr","datePosted":"2026-06-17T03:31:31.394Z","dateModified":"2026-06-17T03:31:31.394Z","hiringOrganization":{"@type":"Organization","name":"S4 Analytics","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Florida","addressRegion":"NY","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"28a9f6866ef94f20c0259c1e"},"url":"https://jobsearcher.com/jobs/28a9f6866ef94f20c0259c1e"}}