{"schemaVersion":"jobsearcher.job.v1","id":"7fd5b95d83e13c0c1d0d2c7c","url":"https://jobsearcher.com/jobs/7fd5b95d83e13c0c1d0d2c7c","canonicalUrl":"https://jobsearcher.com/jobs/7fd5b95d83e13c0c1d0d2c7c","title":"Process Validation Engineer cGMP, Data-Driven QA","description":"PolyPeptide US is seeking a Process Validation Specialist in Torrance, CA for a full-time engagement. You will support process validation activities, including IQ/OQ/PQ, and collaborate with Manufacturing, Quality, Engineering, and R&D to ensure compliant, reproducible manufacturing.\nThis role requires strong technical writing, data review, and risk-based validation decisions in a fast-paced cGMP environment, with opportunities to contribute to scale-ups and technology transfers.\n\n#J-18808-Ljbffr","company":"Polypeptide Us","rawCompany":"polypeptide us","city":"Industry","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-08-03T03:17:48.577Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"}],"industries":[{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Validation Engineer cGMP, Data-Driven QA","description":"PolyPeptide US is seeking a Process Validation Specialist in Torrance, CA for a full-time engagement. You will support process validation activities, including IQ/OQ/PQ, and collaborate with Manufacturing, Quality, Engineering, and R&D to ensure compliant, reproducible manufacturing.\nThis role requires strong technical writing, data review, and risk-based validation decisions in a fast-paced cGMP environment, with opportunities to contribute to scale-ups and technology transfers.\n\n#J-18808-Ljbffr","datePosted":"2026-08-03T03:17:48.577Z","dateModified":"2026-08-03T03:17:48.577Z","hiringOrganization":{"@type":"Organization","name":"Polypeptide Us","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Industry","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"7fd5b95d83e13c0c1d0d2c7c"},"url":"https://jobsearcher.com/jobs/7fd5b95d83e13c0c1d0d2c7c"}}