GenScript

(Sr.) EHS Manager

GenScript$100K — $150K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree or higher in Environmental Science, Occupational Health & Safety, Industrial Hygiene, Engineering, Biology, or related field.
  • 10+ years of EHS experience in a biotech/pharma/CDMO or similar environment.
  • Experience with biologics or viral vector operations, specifically within BSL-2 labs and GMP manufacturing, is strongly preferred.
  • Solid understanding of OSHA regulations, RCRA, CAA/CWA, and DOT HazMat requirements; knowledge of biosafety standards is a plus.
  • Preferred certifications include CSP, CIH, CHMM, RBP/CBSP or equivalent certification.
  • Ability to work effectively across teams and communicate operational EHS solutions in a fast-paced environment.

Responsibilities

  • Own and manage the EHS Management System to ensure compliance with regulations.
  • Develop and implement EHS policies, procedures, and programs.
  • Lead initiatives for environmental compliance including waste management and air emissions.
  • Oversee biosafety programs for plasmid and lentiviral operations.
  • Ensure safe handling of biological materials and chemicals.
  • Coordinate industrial hygiene assessments and health programs.
  • Lead EHS risk assessments, incident investigations, and track EHS KPIs.

Benefits

  • Comprehensive health and wellness program
  • Ongoing professional development opportunities
  • Generous PTO and holiday leave
  • Retirement savings plan options
  • Employee assistance and counseling services
Full Job Description


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.

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About GenScript

GenScript Biotech Corporation is a global biotechnology group headquartered in Piscataway, New Jersey, United States. The company provides biological research services and products to scientists in pharmaceutical, biotechnology, agricultural, and academic settings. The company's services include gene synthesis, peptide synthesis, protein expression, antibody development, and in vitro and in vivo pharmacology studies. The company's products include molecular biology reagents, peptides, proteins, antibodies, and cell line development services. The company has subsidiaries in the United States, Europe, Japan, and China. GenScript was founded in 2002 by Frank Zhang and has grown to become a leading provider of gene synthesis services and other biotechnology products and services.
Learn more about GenScript
Size
3,000 employees
Industry
Founded
2002

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