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AGC Biologics

End-to-end biopharma CDMO for gene therapies

EHS Manager

Environmental Health & SafetyConfirmed live in the last 24 hours
Full-timeHeidelberg, GermanyIn-person

About the Job

Requirements

  • A completed degree in natural sciences or engineering, or an equivalent qualification.
  • At least 3 years of professional experience in EHS within the process industry.
  • Knowledge of Good Manufacturing Practice is desirable.
  • Strong teamwork and communication skills, with the ability to motivate and inspire others.
  • Very good German and good English skills, spoken and written.
  • A goal-oriented, independent, and execution-focused working style.
  • Qualification as an occupational safety specialist is desirable, or willingness to obtain it during employment.
  • Valid work and residence permits.

Responsibilities

  • Monitor, develop, and optimize occupational safety standards and policies, accident prevention, and environmental protection.
  • Serve as a contact for authorities on occupational health and safety, environmental protection, and permits.
  • Prepare workplace assessments, risk assessments, operating instructions, and risk analyses for new materials and processes.
  • Coordinate measures to promote employee EHS awareness, prepare training materials, and conduct training on EHS topics.
  • Manage external contractors, particularly within investment projects.
  • Plan and conduct inspections and audits, and follow up on agreed actions to ensure EHS compliance.
  • Maintain certification and develop the site's EHS management systems, including ISO 14001 and ISO 45001, and ensure compliance with AGC Biologics requirements.
  • Acquire specialized EHS knowledge related to biotechnology.

Desired Qualifications

  • Knowledge of Good Manufacturing Practice.
  • Qualification as an occupational safety specialist, or willingness to obtain it during employment.

About the Company

AGC Biologics

End-to-end biopharma CDMO for gene therapies

AGC Biologics is a global contract development and manufacturing organization (CDMO) that develops and manufactures biopharmaceuticals, including therapeutic proteins, plasmid DNA, viral vectors, and cell therapies. It offers end-to-end services from early development through commercial-scale manufacturing, with fast-track options for orphan drugs and rare diseases. The company runs cGMP-compliant facilities across the US, Europe, and Asia, recently expanding with a Longmont, Colorado site focused on cell and gene therapies. Its goal is to help biopharma partners bring new treatments to market efficiently and safely by providing integrated development and manufacturing, supported by its international footprint and project acceleration capabilities.

Company size
1,001-5,000
Company stage
Acquired
Total funding
$557.7M
Headquarters
Bothell, WA
Founded
2001

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