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Landmark Bio

Cell and gene therapy CDMO services

Manager – Environmental Health & Safety - Environmental Health & Safety

Full-TimeUpdated on 10/23/2026
No salary listed
Senior
Bachelor's, Master's
Watertown, MA, USA
In PersonOn-site role requiring regular presence in laboratory, manufacturing, office, and facility environments.
Facilities OperationsEnvironmental Health & Safety

About the job

Requirements
  • A bachelor's degree in Environmental Health & Safety, Occupational Health and Safety, Environmental Science, Industrial Hygiene, Engineering, Life Sciences, or a related field is required.
  • Approximately 5–8 years of progressive EHS experience, preferably within biotechnology, pharmaceutical, life sciences, manufacturing, laboratory, or other regulated environments.
  • Working knowledge of OSHA, EPA, Massachusetts environmental and workplace safety requirements, and other applicable federal, state, and local regulations.
  • Demonstrated experience developing and implementing EHS programs, policies, procedures, and employee training.
  • Experience conducting risk assessments, incident investigations, root cause analyses, and corrective action planning.
  • Knowledge of hazardous materials management, hazardous waste, chemical safety, emergency response, and occupational safety programs.
  • Strong project management, organizational, and documentation skills to manage multiple priorities.
  • Ability to communicate complex regulatory and safety requirements clearly and practically.
  • Ability to work independently in a highly collaborative, fast-paced environment.
  • Ability to conduct facility inspections and respond to safety-related matters throughout the site.
Responsibilities
  • Lead the development, implementation, and continuous improvement of company-wide EHS programs, policies, procedures, and training.
  • Serve as the primary EHS subject matter expert and partner with site leadership and functional teams to identify, assess, and mitigate workplace hazards.
  • Ensure compliance with applicable federal, state, and local environmental, health, and safety regulations and requirements, including OSHA, EPA, DEP, and other applicable agencies.
  • Conduct workplace safety inspections, risk assessments, job hazard analyses (JHAs/JSAs), and ergonomic evaluations, and recommend corrective and preventive actions.
  • Manage incident reporting, investigation, root cause analysis, corrective actions, and follow-up for workplace injuries, near misses, spills, and other safety events.
  • Develop, coordinate, and deliver EHS training programs, including new-hire orientation, contractor training, respiratory protection, role-specific training, and web-based options covering relevant regulatory topics.
  • Manage hazardous materials, chemical safety, hazardous waste, biological safety, and related environmental compliance programs.
  • Oversee biosafety programs, including risk assessments for biological materials, biosafety level determinations, and coordination with institutional biosafety processes as applicable.
  • Maintain and oversee Safety Data Sheets, chemical inventories, hazard communication, PPE requirements, and laboratory and manufacturing safety programs.
  • Partner with Facilities and Engineering on emergency preparedness, fire and life safety, contractor safety, equipment safety, and facility-related EHS initiatives.
  • Support biosafety and laboratory safety programs appropriate for biotechnology and advanced therapy operations.
  • Coordinate emergency response planning, drills, evacuation procedures, and business continuity-related safety activities.
  • Facilitate safety committees and promote employee engagement in safety initiatives.
  • Manage occupational health and safety requirements and coordinate with HR and external partners as appropriate for workers' compensation and return-to-work matters.
  • Track, analyze, and report EHS metrics, trends, incidents, and corrective actions to leadership; maintain a compliance calendar and required EHS records, permits, documentation, and regulatory reporting.
  • Support internal and external audits, regulatory inspections, and client or partner assessments related to EHS.
  • Partner with Quality and operational teams to ensure EHS requirements are appropriately integrated into cGMP activities and change management processes.
  • Manage external EHS consultants, service providers, and vendors as needed.
  • Advance a proactive safety culture through best practices, employee engagement activities, sustainability initiatives, continuous improvement of EHS programs, and identification of operational efficiencies.
  • Remain current on changes to EHS regulations and industry best practices and recommend updates to company programs as needed.
  • Perform other EHS-related responsibilities and projects as assigned.
  • Work on-site with regular presence in laboratory, manufacturing, office, and facility environments.
  • Occasionally work outside normal business hours to support incidents, emergency response, training, or operational needs.
Desired Qualifications
  • Experience supporting laboratory, manufacturing, and/or cGMP environments is strongly preferred.
  • An advanced degree is preferred.
  • Professional certifications such as CSP, CIH, CHMM, ASP, or similar credentials are preferred but not required.

About the company

Landmark Bio is a contract development and manufacturing organization (CDMO) focused on cell and gene therapy. It provides end-to-end services including drug development consulting, process analytical development, cGMP manufacturing, and CMC regulatory consulting to turn research into clinical programs. Its offerings are tailored services rather than products, delivered through collaborations with academia, physicians, biopharma, and research hospitals to address manufacturing costs and complexities. Its goal is to help programs reach clinical trials and commercial use faster while meeting regulatory standards and budget constraints, increasing patient access to advanced therapies.

Company Size

51-200

Company Stage

N/A

Total Funding

N/A

Headquarters

Watertown, Massachusetts

Founded

N/A

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Simplify's Take

What believers are saying

  • ARPA-H awarded up to $18.3 million in April 2026 for TRANSFORM-EV.
  • Mass General Brigham collaboration can funnel recurring early-stage projects into Watertown.
  • ChromaTan and Landmark Bio won NIIMBL support for scalable AAV manufacturing platform development.

What critics are saying

  • Artis BioSolutions controls Landmark Bio, so a parent funding pullback hits operations immediately.
  • ARPA-H TRANSFORM-EV lasts three years; failed milestones would weaken Landmark Bio’s follow-on credibility.
  • Cell-therapy CDMO demand stays lumpy; losing Galapagos or InnDura programs would cut utilization fast.

What makes Landmark Bio unique

  • Landmark Bio’s 44,000-square-foot Watertown facility offers end-to-end CGT development and GMP manufacturing.
  • Artis BioSolutions acquired Landmark Bio in April 2025, adding broader genetic-medicine scale.
  • Mass General Brigham partnered with Landmark Bio in October 2025 for translational cell and gene therapies.

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Benefits

  • Health Insurance
  • Unlimited Paid Time Off
  • Flexible Work Hours
  • Hybrid Work Options
  • Professional Development Budget
  • Conference Attendance Budget
  • Wellness Program
  • Mental Health Support
  • Stock Options
  • Company Equity
  • 401(k) Retirement Plan
  • 401(k) Company Match

Company News

Connect Iredell
Apr 16th, 2026
Landmark Bio secures up to $18.3M ARPA-H funding for EV manufacturing platform

Landmark Bio has secured up to $18.3 million in funding from ARPA-H through its TRANSFORM-EV programme, with support from national advisory firm EverGlade. The three-year award will fund development of a continuous manufacturing platform for extracellular vesicles, potentially benefiting advanced therapies including viral vectors and cell therapies. The project aims to overcome current low-yield, high-cost batch manufacturing methods by integrating advanced upstream, downstream and analytical technologies. EverGlade supported Landmark Bio through negotiations, including multiple redesigns of work statements, milestones and financial documentation. EverGlade specialises in helping innovators navigate federal funding from agencies including ARPA-H, BARDA and DARPA. Landmark Bio, an Artis BioSolutions company, operates from Watertown, Massachusetts, providing process development and GMP manufacturing for advanced therapies.

Business Wire
Feb 17th, 2026
Artis BioSolutions names Dr Kate Broderick chief scientific innovation officer to advance synthetic DNA strategy

Artis BioSolutions has appointed Dr Kate Broderick as Chief Scientific Innovation Officer, effective 9 February 2026. She will lead scientific strategy and innovation initiatives across the company's platform for developing and manufacturing genetic medicines. Dr Broderick brings over 25 years of experience in nucleic acid medicine and DNA- and RNA-based vaccine development. Most recently, she served as Chief Innovation Officer at Maravai LifeSciences. Previously, at Inovio Pharmaceuticals, she led R&D teams that advanced multiple clinical-stage programmes, including a DNA-based COVID-19 vaccine through Phase 3 testing, and secured over $100 million in non-dilutive funding. The appointment comes as Artis prepares to close its acquisition of Syngoi Technologies, expected in the first quarter of 2026. Dr Broderick holds a PhD in Molecular Genetics from the University of Glasgow.

Business Wire
Apr 3rd, 2025
Artis BioSolutions Emerges from Stealth, Announces Acquisition of Landmark Bio

Artis BioSolutions, a company founded to streamline the discovery, development and production of genetic medicines, today announced its launch, alongside its...