About the role
About GenScript
GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.
About Probio:
ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to GMP for plasmids, antibodies, and cell & gene therapies. We bring together multidisciplinary expertise to accelerate development and manufacturing through customized, and comprehensive services. ProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017.
Position Summary
(Sr.) EHS Manager is responsible for establishing, leading, and continuously improving the EHS program for a single-site biologics and GCT CDMO in New Jersey, covering process development (PD) through GMP manufacturing of plasmid DNA, viral vectors and biologics. This 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.
Key Responsibilities
- Own and manage the site EHS Management System in compliance with OSHA, EPA, DOT, NFPA, and NJ state/local regulations.
- Develop, maintain, and implement EHS policies, procedures, and programs.
- Lead environmental compliance: hazardous/universal waste, wastewater, air emissions, Tier II/SARA reporting, and NJDEP permits.
- Lead or support the Biosafety Officer function; oversee biosafety programs for BSL-2 / BSL-2+ plasmid and lentiviral operations.
- Ensure safe handling and control of viral vectors, biological materials, chemicals, cryogens (LN2), and compressed gases.
- Plan and coordinate industrial hygiene assessments and occupational health programs (e.g., respiratory protection, medical surveillance).
- Lead EHS risk assessments, incident/near-miss investigations, root cause analysis, and CAPA; track and report EHS KPIs.
- Deliver EHS onboarding and refresher training; maintain strong floor presence and coach line leadership.
- Represent EHS during client audits, regulatory inspections, and site visits; support EHS sections of quality/technical agreements.
- Own the site Emergency Response Plan and coordinate drills and external responder engagement.
Qualifications
- Bachelor’s or above degree in Environmental Science, Occupational Health & Safety, Industrial Hygiene, Engineering, Biology, or related field required.
- 10+ years of EHS experience with site-level responsibility in biotech/pharma/CDMO or similar regulated environment.
- Strongly preferred: experience with biologics or viral vector operations (plasmid DNA, lentivirus, BSL-2 labs, GMP manufacturing).
- Solid knowledge of OSHA 29 CFR 1910, RCRA, basic CAA/CWA requirements, DOT HazMat; familiarity with biosafety standards (BMBL, NIH Guidelines).
- Preferred certifications: CSP, CIH, CHMM, RBP/CBSP or equivalent.
- Proven ability to work cross-functionally, communicate clearly, and provide practical, operations-friendly EHS solutions in a fast-paced setting.
The estimated salary range is $100,000 - $150,000, based on experience level.
#LW
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GenScript 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.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.
Aplyr's read
GenScript is a leading biotechnology firm specializing in gene and peptide synthesis, attracting scientific minds and business professionals alike to innovate in life sciences.
What's promising
- •GenScript is a pioneer in gene synthesis, offering cutting-edge solutions to the biotech industry.
- •The company invests heavily in R&D, providing ample opportunities for scientific innovation and career growth.
- •GenScript's global presence allows for diverse career opportunities and international collaboration.
What to watch
- •The biotechnology sector is highly competitive, posing challenges for market differentiation.
- •Rapid technological advancements may require continuous skill updates for employees.
- •Limited public information about work-life balance and company culture.
Why Genscript
- •GenScript's focus on gene and peptide synthesis sets it apart in the biotech landscape.
- •The company offers specialized roles in AI research, blending technology with biotech innovation.
- •GenScript's global operations provide a platform for cross-border scientific collaboration.
Aplyr’s read is generated by AI from public sources. Was it useful?
About Genscript
GenScript is a global biotechnology company that provides gene synthesis, peptide synthesis, and other related services to researchers and companies in the life sciences sector.
