{"schemaVersion":"jobsearcher.job.v1","id":"849014d10bd0f75a64a9ba3b","url":"https://jobsearcher.com/jobs/849014d10bd0f75a64a9ba3b","canonicalUrl":"https://jobsearcher.com/jobs/849014d10bd0f75a64a9ba3b","title":"(Sr) Technician, Upstream Process","description":"About the job:\nThe (Sr) Technician, Upstream Process will work within the Upstream Processing group and performs the following activities while executing upstream operations:\n\nPreparation of stock solutions, buffers and media.\n\nFiltration of stock solutions, buffers and media.\n\nSet‑up and operate disposable fermenters / bioreactors and other disposable bioprocess equipment including depth filtration.\n\nPassage and expansion of microbial and mammalian cell lines.\n\nThe (Sr) Technician, Upstream Process supports relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.\n\nResponsibilities:\n\nExecutes routine complex manufacturing assignments per written procedures; recognizes deviations from procedures and raises issue to management for resolution.\n\nAdheres to cGMP and SOPs.\n\nPerforms routine microbial and mammalian cell culture using aseptic techniques; monitors microbial fermenters and mammalian cell cultures bioreactors.\n\nWeighs and checks raw materials, assembles process equipment, and monitors processes.\n\nCompletes work instructions and maintains a clean‑room environment to comply with regulatory requirements; removes red bag waste as required.\n\nOperates all production equipment in assigned functional area such as disposable fermenters, bioreactors, other disposable bioprocess equipment, and media preparation equipment per written procedures.\n\nAuthors solution preparation Master Batch Records (MBRs) by transferring technical information from scientific and development documents.\n\nProposes and routes revisions to existing SOPs for functional area equipment.\n\nWorks to become proficient on common bioprocessing equipment.\n\nParticipates in low‑risk deviations investigations; assists in the implementation of Corrective Action / Preventative Actions (CAPA) action items within agreed upon timelines.\n\nConducts safety and GMP self‑auditing walkthroughs, documenting observations for assignment and closure dates; tracks and ensures closure of observations.\n\nLogs and submits samples in Laboratory Information Management System (LIMS); tracks results and compiles data.\n\nReviews own work for completeness on executed MBRs.\n\nCoordinates the tracking and return of executed records to the Quality department for review.\n\nCoordinates with Logistics to ensure needed materials are delivered to the production area timely; monitors future needs against material supply to alert Logistics of shortfalls.\n\nPerforms other tasks and assignments as needed and specified by management.\n\nQualifications:\n\nBachelor’s degree in science or engineering with 0–5 years relevant experience, or Associate’s degree with a minimum of 3 years, or High school diploma with a minimum of 7 years of relevant experience.\n\nDemonstrated ability to follow written instructions and procedures.\n\nDemonstrated ability to pay strict attention to detail.\n\nProficiency with Microsoft Office.\n\nExcellent verbal and written communication skills.\n\nAbility to work collaboratively as part of a team in a fast‑paced, matrixed, team environment consisting of internal and external team members.\n\nThe estimated pay range for the role is between $60,000 - $75,000 based on qualifications and experience.\n\nGenScript USA Inc./ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.\n\nGenScript USA Inc./ProBio Inc. maintains a drug‑free workplace.\n\n#J-18808-Ljbffr","company":"Genscript","rawCompany":"genscript","city":"Pennington","state":"NJ","isRemote":false,"isActive":false,"createdAt":"2026-06-24T03:20:08.858Z","occupations":[{"code":"19-4021.00","title":"Biological Technicians","slug":"biological-technicians"},{"code":"19-4099.00","title":"Life, Physical, and Social Science Technicians, All Other","slug":"life-physical-and-social-science-technicians-all-other"},{"code":"51-8099.01","title":"Biofuels Processing Technicians","slug":"biofuels-processing-technicians"}],"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":"(Sr) Technician, Upstream Process","description":"About the job:\nThe (Sr) Technician, Upstream Process will work within the Upstream Processing group and performs the following activities while executing upstream operations:\n\nPreparation of stock solutions, buffers and media.\n\nFiltration of stock solutions, buffers and media.\n\nSet‑up and operate disposable fermenters / bioreactors and other disposable bioprocess equipment including depth filtration.\n\nPassage and expansion of microbial and mammalian cell lines.\n\nThe (Sr) Technician, Upstream Process supports relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.\n\nResponsibilities:\n\nExecutes routine complex manufacturing assignments per written procedures; recognizes deviations from procedures and raises issue to management for resolution.\n\nAdheres to cGMP and SOPs.\n\nPerforms routine microbial and mammalian cell culture using aseptic techniques; monitors microbial fermenters and mammalian cell cultures bioreactors.\n\nWeighs and checks raw materials, assembles process equipment, and monitors processes.\n\nCompletes work instructions and maintains a clean‑room environment to comply with regulatory requirements; removes red bag waste as required.\n\nOperates all production equipment in assigned functional area such as disposable fermenters, bioreactors, other disposable bioprocess equipment, and media preparation equipment per written procedures.\n\nAuthors solution preparation Master Batch Records (MBRs) by transferring technical information from scientific and development documents.\n\nProposes and routes revisions to existing SOPs for functional area equipment.\n\nWorks to become proficient on common bioprocessing equipment.\n\nParticipates in low‑risk deviations investigations; assists in the implementation of Corrective Action / Preventative Actions (CAPA) action items within agreed upon timelines.\n\nConducts safety and GMP self‑auditing walkthroughs, documenting observations for assignment and closure dates; tracks and ensures closure of observations.\n\nLogs and submits samples in Laboratory Information Management System (LIMS); tracks results and compiles data.\n\nReviews own work for completeness on executed MBRs.\n\nCoordinates the tracking and return of executed records to the Quality department for review.\n\nCoordinates with Logistics to ensure needed materials are delivered to the production area timely; monitors future needs against material supply to alert Logistics of shortfalls.\n\nPerforms other tasks and assignments as needed and specified by management.\n\nQualifications:\n\nBachelor’s degree in science or engineering with 0–5 years relevant experience, or Associate’s degree with a minimum of 3 years, or High school diploma with a minimum of 7 years of relevant experience.\n\nDemonstrated ability to follow written instructions and procedures.\n\nDemonstrated ability to pay strict attention to detail.\n\nProficiency with Microsoft Office.\n\nExcellent verbal and written communication skills.\n\nAbility to work collaboratively as part of a team in a fast‑paced, matrixed, team environment consisting of internal and external team members.\n\nThe estimated pay range for the role is between $60,000 - $75,000 based on qualifications and experience.\n\nGenScript USA Inc./ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.\n\nGenScript USA Inc./ProBio Inc. maintains a drug‑free workplace.\n\n#J-18808-Ljbffr","datePosted":"2026-06-24T03:20:08.858Z","dateModified":"2026-06-24T03:20:08.858Z","hiringOrganization":{"@type":"Organization","name":"Genscript","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pennington","addressRegion":"NJ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"849014d10bd0f75a64a9ba3b"},"url":"https://jobsearcher.com/jobs/849014d10bd0f75a64a9ba3b"}}