Environmental Compliance & EMS Lead (ISO 14001)

Simtra BioPharma Solutions

Bloomington (IN)

On-site

USD 90,000 - 130,000

Full time

2 days ago
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Benefits offered by this job

Day One Benefits
Medical & Dental Coverage
401(k) Retirement Savings Plan with 1:

Job summary

Simtra BioPharma Solutions in Bloomington, IN, seeks an Environmental Manager to lead regulatory compliance, EMS implementation, and environmental risk management on site. The role reports to EHS&S leadership and partners with Operations, Engineering, Quality, and Supply Chain to embed sustainable practices across capital projects and processes.

The ideal candidate brings experience in pharmaceutical manufacturing regulatory programs, ISO 14001, and strong stakeholder collaboration to drive

Qualifications

  • BS in Environmental Science or related field.
  • Experience with pharmaceutical/CDMO environmental compliance.
  • ISO 14001 or similar EMS implementation experience.

Responsibilities

  • Lead regulatory compliance program for site (EPA/IDEM).
  • Develop and maintain ISO 14001‑aligned EMS and KPIs.
  • Oversee waste, air, water permits and reporting.
  • Coordinate audits and regulator inquiries with cross‑functional teams.
  • Guide waste management, chemical handling and SDS controls.
  • Improve environmental performance and risk reduction across operations.

Skills

Regulatory compliance
ISO 14001
Environmental audits
Hazardous waste
Air & water permits
Project management
Cross‑functional leadership
Chemical management
SDS compliance

Education

BS in Environmental Science
ISO 14001 Lead Auditor

Tools

VelocityEHS
Regulatory databases

Job description

Simtra BioPharma Solutions in Bloomington, IN, seeks an Environmental Manager to lead regulatory compliance, EMS implementation, and environmental risk management on site. The role reports to EHS&S leadership and partners with Operations, Engineering, Quality, and Supply Chain to embed sustainable practices across capital projects and processes.

The ideal candidate brings experience in pharmaceutical manufacturing regulatory programs, ISO 14001, and strong stakeholder collaboration to drive

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