BeiGene, Ltd.

: Associate EHS (Environmental, Health, and Safety) Manager

BeiGene, Ltd.$95K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in science, engineering, or technology with 4+ years' experience; or a relevant Master’s degree with 2 years' experience
  • Strong organizational skills
  • Highly developed verbal and written communication skills, fluency in English required, Spanish proficiency desirable
  • Experience in EHS regulatory program requirements in a biotech research lab or GLP setting preferred
  • Desirable certifications include CSP, CHMM, CIH, EMT, HAZWOPER, first aid, CPR, AED

Responsibilities

  • Perform hazard, risk, exposure, and ergonomic assessments using enterprise EHS software
  • Support the development and improvement of EHS programs for lab and office operations
  • Maintain compliance with California-specific EHS regulations
  • Serve as a resource for laboratory staff on safe work practices
  • Promote a strong safety culture through engagement and initiatives
  • Support the onboarding of new employees with EHS training
  • Implement the biosafety program for BSL-2 laboratories

Benefits

  • Comprehensive benefits package including Medical, Dental, and Vision
  • 401(k) with potential company contributions
  • Flexible Spending Account (FSA) and Health Savings Account (HSA) options
  • Paid Time Off to promote work-life balance
  • Wellness programs to support employee health
  • Eligibility for annual bonus plan and discretionary equity awards
  • Participation in the Employee Stock Purchase Plan
Full Job Description

General Description:

The Associate EHS Manager will play a key role in supporting and advancing the EHS program at our pharmaceutical research and corporate office location in San Carlos, California.  This position partners closely with laboratory leadership, researchers, and facilities engineering to ensure a safe, compliant, and sustainable work environment while meeting all applicable federal, state, and local EHS regulations. The responsibilities also include EHS aspects of our corporate office operations in San Carlos and US remote employees.  

Technical compliance programs will include biosafety and laboratory safety, chemical management, hazardous waste compliance, emergency preparedness and response, industrial hygiene, ergonomics, various OSHA programs, as well as sustainability.  This role will also support EHS efforts for our small-scale South American QC laboratories as well as provide support to overall US EHS operations as needed.  Approximately 10% travel.     

Although the position is mainly an administrative function, there are also hands-on requirements in terms of implementing hazardous waste / chemical management programs, emergency response, sampling/analysis, auditing, inspections, etc.                  

Essential Functions of the job:

  • Perform hazard/risk/exposure/ergonomic assessments for current and future processes and track through closure using our enterprise EHS software. 

  • Support the development, implementation, and continuous improvement of EHS programs for laboratory and support operations, including Injury & Illness Prevention Program (IIPP), Chemical Hygiene Plan, Hazard Communication, Emergency Action Plans, compliance with Bay Area Air Quality regulations, and safety programs in accordance with Cal/OSHA and federal OSHA requirements.

  • Assist in maintaining compliance with California‑specific regulatory requirements including Cal/OSHA Title 8, Department of Toxic Substances Control (DTSC), and local Certified Unified Program Agency (CUPA) requirements.     

  • Serve as a day‑to‑day EHS resource for laboratory staff, providing guidance on safe work practices and regulatory expectations.

  • Promote a strong safety culture by engaging researchers and managers in hazard identification, EHS Gemba, near‑miss reporting, and continuous improvement initiatives.

  • Support onboarding of new employees and contractors with EHS orientations and lab‑specific safety requirements (e-learning and live sessions).

  • Support biosafety program implementation for BSL‑2 laboratories, ensuring alignment with CDC/NIH Biosafety in Microbiological and Biomedical Laboratories (BMBL) guidance and institutional biosafety requirements.

  • Accountable for EHS regulatory preparedness and participation in regulatory inspections, self-assessments, and audits.   

  • Conduct incident investigations involving biological exposures, chemical spills, injuries, determine root cause, implement and track robust corrective actions to completion.

  • Perform Industrial hygiene (IH) assessments and testing in accordance with industry standards and/or lead the efforts for overseeing 3rd party IH, sampling efforts, etc.   

  • Develop online training programs and work with remote and office employees toward prevention and/or resolution of ergonomic and other office related EHS issues such as drivers’ safety.

  • Ability to apply EHS regulatory program requirements in a GLP operational setting and coach team members & operation leaders to enable them to successfully deploy EHS best practices.

  • Responsible for utilizing EHS platforms such as Velocity EHS for investigations, inspections, chemical management, approvals, dashboards upkeep, and compliance activities.

  • Active engagement in EHS training programs and development and delivery of curricula.

  • Must be accountable, have sound judgment, excellent analytical and problem-solving skills and be directly involved to deliver practical solutions.

  • Lead EHS Committee, ERT, and audits teams. 

Qualifications:

  • Bachelor’s degree in science, engineering or technology with 4+ years’ experience or relevant Master’s degree with 2 years experience.

  • Strong organizational skills.

  • Highly developed verbal and written communication skills.  Fluency in English required.  Spanish proficiency is desirable.    

  • Experience in applying EHS regulatory program requirements in a biotech research lab, GLP operational setting, or engineering services firm, desired.

  • Certifications such as CSP, CHMM, CIH, EMT, etc. desired, in addition to HAZWOPER, 1st aid, CPR, AED      

Supervisory Responsibilities:

Lead in a matrix environment

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $95,800.00 - $130,800.00 annually

BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process.  Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

About BeiGene, Ltd.

BeiGene, Ltd. is a biotechnology company that develops and commercializes innovative cancer treatments. The company was founded in 2010 and is headquartered in George Town, Grand Cayman. BeiGene's portfolio includes several drug candidates that target cancer cells and the tumor microenvironment. The company's lead product, Brukinsa, is a treatment for mantle cell lymphoma that has been approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). BeiGene also has partnerships with several pharmaceutical companies, including Amgen, Merck, and Novartis.
Learn more about BeiGene, Ltd.
Size
8,300 employees
Market Cap
$22.2 billion
Industry
Net Income
-$1.5 billion
Founded
2010
5 Year Trend
+305.7%
Revenue
$308.8 million
NASDAQ

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