EHS Associate

Posted 11 Days Ago
Be an Early Applicant
North Chicago, IL
3-5 Years Experience
Pharmaceutical
The Role
The EHS Associate will support ISO certification processes, conduct risk management assessments, facilitate audits, and maintain ISO documentation for a global pharmaceutical manufacturing company.
Summary Generated by Built In


The Environmental Health & Safety (EHS) Associate will support the facility with ISO certification process for multiple facilities within a global pharmaceutical manufacturing company. This person will be responsible for conducting risk management assessments, facilitating ISO facility audits and certifications, and creating and maintaining ISO-related documentation, among other duties.

Responsibilities

  • Manage and maintain company's ISO 14001, 45001, and 50001 Management Systems to ensure compliance and continuous improvement.
  • Conduct risk assessments and implement risk management strategies to mitigate potential hazards.
  • Support facility audits and ISO certification processes.
  • Review associated paperwork to ensure compliance, as well as create / maintain ISO-related documents as required.
  • Support facility improvements by conducting GEMBA walks.

Requirements

  • Bachelor's degree in Science, Chemical Engineering, Mechanical Engineering or Business Administration.
  • 2-5 years of experience in a Environmental, Health, and Safety (EHS) with a focus in ISO standards.
  • A strong understanding of ISO 45001 (workplace safety), ISO 14001 (environmental systems) and ISO 50001 (energy management).
  • Experience with risk management, ability to work cross-functionally, communicate effectively and execute.
The Company
HQ: Lake Forest, IL
68 Employees
On-site Workplace
Year Founded: 2001

What We Do

Founded in 2001, cGMP Consulting Inc. has strived to help our clients adopt new technologies and ensure that changes to your processes are compliant with current Good Manufacturing Practices (cGMP). Our experienced engineering and quality assurance consultants have helped many industry leading companies identify and remediate gaps, support international pharmaceutical manufacturing, and implement cGMP requirements.

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