{"schemaVersion":"jobsearcher.job.v1","id":"893352472bd44ffb05cb554e","url":"https://jobsearcher.com/jobs/893352472bd44ffb05cb554e","canonicalUrl":"https://jobsearcher.com/jobs/893352472bd44ffb05cb554e","title":"Assistant Process Engineer","description":"50% onsite required\nWork Schedule: Mon-Fri (normal business hours)\n\nMust Haves:\nBachelor's degree required\nExperience in Technical writing such as SOPs, protocols, summary reports and/or change controls.\n\nThe Senior Specialist, MS&T Validation provides process validation support to the Devens Cell Therapy Facility (CTF). The Senior Specialist participates in facility, process, and aseptic validation activities, including support of the Aseptic Process Simulation Program and implementation of process lifecycle management changes.\n\nJob Responsibilities:\n\nResponsible for oversight of CTF Process Validation activities including, but not limited to Aseptic Process Simulations/ Validations (APS/APV), and other Lifecycle Management changes.\n\nPrepares written protocols/reports/summaries supporting validation studies.\n\nEnsures safe and compliant cGMP operations, maintains permanent inspection readiness.\n\nThis position reports to the Associate Director of Manufacturing Science and Technology Validation.\n\nSpecific Knowledge, Skills, Abilities:\n\nExperience in cGMP’s and multi-national biopharmaceutical/cell therapy regulations\n\nExcellent verbal/written communication skills\n\nEducation/Experience/ Licenses/Certifications\n\nKnowledge of science generally attained through studies resulting in a Bachelor’s degree in science, engineering, biochemistry or related discipline, is required\n\nA minimum of 2 years’ experience in biopharmaceutical operations, or its equivalent is required.\n\nPay: $30.00 - $35.00 per hour\n\nExpected hours: 40.0 per week\n\nWork Location: In person","company":"Synkriom","rawCompany":"synkriom","city":"Devens","state":"MA","isRemote":false,"isActive":false,"createdAt":"2026-10-28T11:25:55.323Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-3026.00","title":"Industrial Engineering Technologists and Technicians","slug":"industrial-engineering-technologists-and-technicians"},{"code":"17-3029.00","title":"Engineering Technologists and Technicians, Except Drafters, All Other","slug":"engineering-technologists-and-technicians-except-drafters-all-other"}],"industries":[{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Assistant Process Engineer","description":"50% onsite required\nWork Schedule: Mon-Fri (normal business hours)\n\nMust Haves:\nBachelor's degree required\nExperience in Technical writing such as SOPs, protocols, summary reports and/or change controls.\n\nThe Senior Specialist, MS&T Validation provides process validation support to the Devens Cell Therapy Facility (CTF). The Senior Specialist participates in facility, process, and aseptic validation activities, including support of the Aseptic Process Simulation Program and implementation of process lifecycle management changes.\n\nJob Responsibilities:\n\nResponsible for oversight of CTF Process Validation activities including, but not limited to Aseptic Process Simulations/ Validations (APS/APV), and other Lifecycle Management changes.\n\nPrepares written protocols/reports/summaries supporting validation studies.\n\nEnsures safe and compliant cGMP operations, maintains permanent inspection readiness.\n\nThis position reports to the Associate Director of Manufacturing Science and Technology Validation.\n\nSpecific Knowledge, Skills, Abilities:\n\nExperience in cGMP’s and multi-national biopharmaceutical/cell therapy regulations\n\nExcellent verbal/written communication skills\n\nEducation/Experience/ Licenses/Certifications\n\nKnowledge of science generally attained through studies resulting in a Bachelor’s degree in science, engineering, biochemistry or related discipline, is required\n\nA minimum of 2 years’ experience in biopharmaceutical operations, or its equivalent is required.\n\nPay: $30.00 - $35.00 per hour\n\nExpected hours: 40.0 per week\n\nWork Location: In person","datePosted":"2026-10-28T11:25:55.323Z","dateModified":"2026-10-28T11:25:55.323Z","hiringOrganization":{"@type":"Organization","name":"Synkriom","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Devens","addressRegion":"MA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"893352472bd44ffb05cb554e"},"url":"https://jobsearcher.com/jobs/893352472bd44ffb05cb554e"}}