Senior Facilities & Compliance Manager

Regeneron Pharmaceuticals, Inc.

City of Rensselaer (NY)

On-site

USD 92,000 - 176,000

Full time

6 days ago
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Job summary

Regeneron Pharmaceuticals, Inc. in Saratoga Springs seeks a Manager, Facilities Maintenance to lead the maintenance, calibration, and modification activities for a highly automated drug substance manufacturing site.

You will supervise a team, coordinate external contractors, and ensure compliance with regulatory standards on a 1st shift, with potential transition to a flexible schedule. You will oversee safety, quality, and efficiency initiatives, manage work requests, and contribute to

Qualifications

  • Bachelor's degree in Engineering or related field.
  • Demonstrated 6+ years of supervisory experience for Associate Manager level, 7+ years for Manager level.

Responsibilities

  • Lead supervision, planning, and scheduling of maintenance, repairs, and modifications for systems and equipment.
  • Oversee contract maintenance personnel and ensure qualification, scope alignment, and regulatory compliance.
  • Identify, evaluate, and implement program and process improvements for safety, quality, efficiency and cost-effectiveness.
  • Manage and prioritize work requests across IOPS Rensselaer satellite locations and maintain stakeholder communication.
  • Contribute to cross-functional projects with SME coordination and execution support.
  • Ensure compliance with GxP/GMP/GLP requirements; maintain inspection readiness.
  • Maintain controlled documentation with proper version control and alignment to quality systems.
  • Support investigations and CAPA within the quality system to prevent recurrence.
  • Perform other related duties to support departmental objectives.

Skills

People leadership
Maintenance planning
Regulatory compliance
Project coordination

Education

BS in Engineering or related field

Job description

Regeneron Pharmaceuticals, Inc. in Saratoga Springs seeks a Manager, Facilities Maintenance to lead the maintenance, calibration, and modification activities for a highly automated drug substance manufacturing site.

You will supervise a team, coordinate external contractors, and ensure compliance with regulatory standards on a 1st shift, with potential transition to a flexible schedule. You will oversee safety, quality, and efficiency initiatives, manage work requests, and contribute to

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