{"schemaVersion":"jobsearcher.job.v1","id":"93fa97d01d9b25e819c91df9","url":"https://jobsearcher.com/jobs/93fa97d01d9b25e819c91df9","canonicalUrl":"https://jobsearcher.com/jobs/93fa97d01d9b25e819c91df9","title":"(Sr.) EHS Manager","description":"GenScript Biotech Corporation\nGenScript is a global biotechnology group founded in 2002 with a presence across North America, Europe, Greater China, and Asia Pacific. Its businesses include Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.\n\nAbout Probio\nProBio, a subsidiary of GenScript, is a global CDMO offering end‑to‑end services from discovery to GMP for plasmids, antibodies, and cell & gene therapies. With facilities in the United States, the Netherlands, South Korea, China (Hong Kong, Shanghai, Nanjing), and other regions, ProBio has supported customers in the United States, Europe, Asia Pacific, and beyond, securing more than 150 IND approvals since October 2017.\n\nPosition Summary\n(Sr.) EHS Manager will establish, lead, and continuously improve the EHS program for a single‑site biologics and GCT CDMO in New Jersey, covering process development through GMP manufacturing of plasmid DNA, viral vectors, and biologics. The role ensures full compliance with federal, state, and local regulations, supports client and corporate requirements, and drives a strong safety culture across labs, pilot, and GMP suites.\n\nKey Responsibilities\n\nOwn and manage the site EHS Management System in compliance with OSHA, EPA, DOT, NFPA, and NJ state/local regulations.\n\nDevelop, maintain, and implement EHS policies, procedures, and programs.\n\nLead environmental compliance: hazardous/universal waste, wastewater, air emissions, Tier II/SARA reporting, and NJDEP permits.\n\nLead or support the Biosafety Officer function; oversee biosafety programs for BSL‑2 / BSL‑2+ plasmid and lentiviral operations.\n\nEnsure safe handling and control of viral vectors, biological materials, chemicals, cryogens (LN2), and compressed gases.\n\nPlan and coordinate industrial hygiene assessments and occupational health programs (e.g., respiratory protection, medical surveillance).\n\nLead EHS risk assessments, incident/near‑miss investigations, root cause analysis, and CAPA; track and report EHS KPIs.\n\nDeliver EHS onboarding and refresher training; maintain strong floor presence and coach line leadership.\n\nRepresent EHS during client audits, regulatory inspections, and site visits; support EHS sections of quality/technical agreements.\n\nOwn the site Emergency Response Plan and coordinate drills and external responder engagement.\n\nQualifications\n\nBachelor’s or above degree in Environmental Science, Occupational Health & Safety, Industrial Hygiene, Engineering, Biology, or related field required.\n\n10+ years of EHS experience with site‑level responsibility in biotech/pharma/CDMO or similar regulated environment.\n\nStrongly preferred: experience with biologics or viral vector operations (plasmid DNA, lentivirus, BSL‑2 labs, GMP manufacturing).\n\nSolid knowledge of OSHA 29 CFR 1910, RCRA, basic CAA/CWA requirements, DOT HazMat; familiarity with biosafety standards (BMBL, NIH Guidelines).\n\nPreferred certifications: CSP, CIH, CHMM, RBP/CBSP or equivalent.\n\nProven ability to work cross‑functionally, communicate clearly, and provide practical, operations‑friendly EHS solutions in a fast‑paced setting.\n\nThe estimated salary range is $100,000 - $150,000, based on experience level.\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":"Initial Therapeutics","rawCompany":"initial therapeutics","city":"Pennington","state":"NJ","isRemote":false,"isActive":true,"createdAt":"2026-06-20T03:50:42.081Z","occupations":[{"code":"19-5011.00","title":"Occupational Health and Safety Specialists","slug":"occupational-health-and-safety-specialists"},{"code":"19-5012.00","title":"Occupational Health and Safety Technicians","slug":"occupational-health-and-safety-technicians"},{"code":"19-2041.00","title":"Environmental Scientists and Specialists, Including Health","slug":"environmental-scientists-and-specialists-including-health"}],"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":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"(Sr.) EHS Manager","description":"GenScript Biotech Corporation\nGenScript is a global biotechnology group founded in 2002 with a presence across North America, Europe, Greater China, and Asia Pacific. Its businesses include Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.\n\nAbout Probio\nProBio, a subsidiary of GenScript, is a global CDMO offering end‑to‑end services from discovery to GMP for plasmids, antibodies, and cell & gene therapies. With facilities in the United States, the Netherlands, South Korea, China (Hong Kong, Shanghai, Nanjing), and other regions, ProBio has supported customers in the United States, Europe, Asia Pacific, and beyond, securing more than 150 IND approvals since October 2017.\n\nPosition Summary\n(Sr.) EHS Manager will establish, lead, and continuously improve the EHS program for a single‑site biologics and GCT CDMO in New Jersey, covering process development through GMP manufacturing of plasmid DNA, viral vectors, and biologics. The role ensures full compliance with federal, state, and local regulations, supports client and corporate requirements, and drives a strong safety culture across labs, pilot, and GMP suites.\n\nKey Responsibilities\n\nOwn and manage the site EHS Management System in compliance with OSHA, EPA, DOT, NFPA, and NJ state/local regulations.\n\nDevelop, maintain, and implement EHS policies, procedures, and programs.\n\nLead environmental compliance: hazardous/universal waste, wastewater, air emissions, Tier II/SARA reporting, and NJDEP permits.\n\nLead or support the Biosafety Officer function; oversee biosafety programs for BSL‑2 / BSL‑2+ plasmid and lentiviral operations.\n\nEnsure safe handling and control of viral vectors, biological materials, chemicals, cryogens (LN2), and compressed gases.\n\nPlan and coordinate industrial hygiene assessments and occupational health programs (e.g., respiratory protection, medical surveillance).\n\nLead EHS risk assessments, incident/near‑miss investigations, root cause analysis, and CAPA; track and report EHS KPIs.\n\nDeliver EHS onboarding and refresher training; maintain strong floor presence and coach line leadership.\n\nRepresent EHS during client audits, regulatory inspections, and site visits; support EHS sections of quality/technical agreements.\n\nOwn the site Emergency Response Plan and coordinate drills and external responder engagement.\n\nQualifications\n\nBachelor’s or above degree in Environmental Science, Occupational Health & Safety, Industrial Hygiene, Engineering, Biology, or related field required.\n\n10+ years of EHS experience with site‑level responsibility in biotech/pharma/CDMO or similar regulated environment.\n\nStrongly preferred: experience with biologics or viral vector operations (plasmid DNA, lentivirus, BSL‑2 labs, GMP manufacturing).\n\nSolid knowledge of OSHA 29 CFR 1910, RCRA, basic CAA/CWA requirements, DOT HazMat; familiarity with biosafety standards (BMBL, NIH Guidelines).\n\nPreferred certifications: CSP, CIH, CHMM, RBP/CBSP or equivalent.\n\nProven ability to work cross‑functionally, communicate clearly, and provide practical, operations‑friendly EHS solutions in a fast‑paced setting.\n\nThe estimated salary range is $100,000 - $150,000, based on experience level.\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":"2026-06-20T03:50:42.081Z","dateModified":"2026-06-20T03:50:42.081Z","hiringOrganization":{"@type":"Organization","name":"Initial Therapeutics","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Pennington","addressRegion":"NJ","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"93fa97d01d9b25e819c91df9"},"url":"https://jobsearcher.com/jobs/93fa97d01d9b25e819c91df9"}}