Safety, Health and Environment (SHE) Lead

General information

 

Safety, Health and Environment (SHE) Lead

The Safety, Health, and Environment (SHE) Lead is responsible for ensuring the development and implementation of SHE programs, fostering a culture of safety, and driving sustainability initiatives. This role supports compliance with regulations and internal standards while spearheading efforts to reduce environmental impact and enhance the organization’s sustainability practices in alignment with our long-term strategic objectives.

Your tasks
  • SHE Strategy and Program Development:
    • Design and implement SHE policies, processes, and standards that meet regulatory requirements and align with company objectives.
    • Continuously evaluate and improve the SHE management system, ensuring alignment with industry best practices.

 

  • Safety and Health Oversight:
    • Lead risk assessments to identify potential safety and health hazards, ensuring robust mitigation measures are in place.
    • Oversee incident investigation processes, identifying root causes and ensuring effective corrective actions are implemented.

 

  • Environmental and Sustainability Initiatives:
    • Develop and lead sustainability programs focusing on energy efficiency, waste reduction, and carbon footprint minimization.
    • Collaborate with operational teams to integrate environmentally sustainable practices into manufacturing and supply chain processes.
    • Monitor and report on key environmental metrics and identify opportunities for improvement.

 

  • Training and Organizational Culture:
    • Develop and deliver targeted training programs to promote awareness and adherence to SHE principles across the organization.
    • Champion a proactive SHE culture, encouraging employee engagement and accountability.

 

  • Regulatory Compliance and Reporting:
    • Ensure all activities comply with local, national, and international SHE regulatory requirements.
    • Own the “Risico Evaluatie en Inventarisatie” process at HALIX.
    • Maintain accurate records and documentation to support audits, certifications, and stakeholder reporting.

 

  • Performance Monitoring and Continuous Improvement:
    • Establish and track SHE performance metrics, using data to identify trends and drive improvements.
    • Stay informed about emerging SHE trends, technologies, and regulations to ensure the organization remains at the forefront of industry standards.

 

  • Key Deliverables:
    • Development and execution of SHE policies and programs aligned with strategic goals.
    • Successful implementation of sustainability initiatives with measurable outcomes.
    • Compliance with all applicable SHE regulations and standards.
    • Comprehensive training programs that enhance SHE awareness and practices.
    • Regular reporting of SHE performance and progress toward sustainability goals.
You have
  • At least a bachelor’s degree in Environmental Science, Occupational Health and Safety, Engineering, or a related field.
  • 7+ years of experience in SHE roles within the biopharmaceutical or related industries.
  • Strong understanding of SHE regulations and industry standards (e.g., EU, OSHA, ISO certifications).
  • Experience with Biological Safety (and acting as Biological Safety Officer) would be preferable.
  • Proven experience in developing and managing SHE and sustainability initiatives.
  • Strong leadership and project management skills, with a collaborative approach to problem-solving.
  • Good knowledge of English, both verbal and written. Dutch advantageous.

 

 

Who are we looking for?
  • Professional self-development in SHE standards and best practices.
  • Results-oriented with a focus on achieving safety, health, and environmental goals.
  • Accountability for ensuring compliance and safety outcomes.
  • Cooperation with cross-functional teams to drive SHE initiatives.
  • Planning & organizing to effectively implement SHE strategies and improvements.
  • Analytical thinking to assess risks, identify trends, and drive corrective actions.
Our offer
  • You will be part of a steadily growing and dynamic biopharmaceutical company offering a great environment for self-starters.
  • A culture that is characterized by entrepreneurial spirit and close and transparent communication. The patient’s well-being is always our top priority. This combination is the basis for an interesting and challenging environment.
  • You will be working in our dynamic headquarters in Leiden.
  • Being part of a company that is focused on excellence in GMP Manufacturing.
  • A competitive salary that matches your responsibilities and experience.
 
Your application
We look forward to hearing from you! We are interested in your CV, but we also want to find out more about your ambitions, your personality and what drives you to apply. So be sure to include a brief cover letter telling us why you are a match for this position. The application process consists of an introduction by the Recruiter, two interviews either via video call or live at our office in Leiden with the Hiring Manager and/or a Department Specialist followed by contract negotiations. Depending on the vacancy, an assessment could be part of the process.
Important notice to search firms and recruitment agencies
HALIX does not accept unsolicited approaches from recruitment agencies and/or search firms (such as, for instance, the sending of resumes) for any job posted on this or a referring website. All recruitment agencies and search firms are required to contact HALIX Recruitment via recruitment@hal-allergy.com to enquire about a potential recruitment or search agreement with HALIX.
HALIX, Bioscience as a Service
HALIX is a fast growing, biopharmaceutical contract development and manufacturing organization (CDMO) focused on viral vector and recombinant protein products. We support our customers with the development & commercialization of biologics enabling the treatment & prevention of life threatening conditions such as cancer, COVID-19, influenza and other infectious diseases. Our state of the art GMP manufacturing facilities and our experienced and dedicated team of people ensures manufacturing capabilities which meet the highest quality standards, a service oriented way of working and a flexible mindset. If you too would like to become part of an innovative and challenging contract development and manufacturing organization (CDMO), then this is a perfect opportunity!
HALIX is headquartered in Leiden, where all disciplines work under one roof, from development to sales. We work in an informal, culturally diverse organization with room for growth and continued personal development. HALIX is located in the middle of the thriving and energetic Leiden Bio Science Park, the largest innovation district of the Netherlands in the field of Life Sciences & Health. The central train station and the ancient city center of Leiden are just a 5 minute bike ride away from our office.