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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Manager Facilities Maintenance

Equipment MaintenanceConfirmed live in the last 24 hours
Full-time$92.2k - $176k /yr

About the Job

Requirements

  • A Bachelor of Science in Engineering or a related field, or an equivalent combination of education and experience, is required.
  • At least 6 years of experience is required for Associate Manager level; at least 7 years is required for Manager level. The level will be determined based on experience.
  • Previous people leadership or supervisory experience is required.
  • Ability to work both the initial and permanent schedules is required.
  • Ability to wear full cleanroom attire and remove jewelry, makeup, and nail adornments while wearing it is required.
  • Ability to meet the physical requirements for the entirety of shifts of up to 10 hours in a cleanroom environment is required, including bending, climbing, crawling, kneeling, reaching, sitting, squatting, walking, standing, driving, hand manipulation, and lifting, pushing, or pulling up to 50 pounds.

Responsibilities

  • Direct, organize, and supervise facility general operations and functions, including calibration and process maintenance teams.
  • Lead the supervision, planning, and scheduling of maintenance, repairs, and modifications for systems and equipment while ensuring safety and quality.
  • Oversee and administer contract maintenance personnel performing repairs and modernization activities, ensuring contractor qualification, scope alignment, and compliance with regulatory and local requirements.
  • Identify, evaluate, and implement program and process improvements that enhance safety, quality, efficiency, and cost-effectiveness.
  • Manage and prioritize work requests to ensure timely completion across IOPS Rensselaer satellite locations and consistent communication with stakeholders.
  • Contribute subject-matter expertise, coordination, and execution support to departmental and cross-functional projects and initiatives.
  • Ensure compliance with applicable GxP, GMP, and GLP requirements, maintain inspection readiness, and support internal, partner, and regulatory audits.
  • Maintain and update controlled documentation with proper version control, accuracy, and alignment to quality system requirements.
  • Support event and deviation investigations and drive or facilitate corrective and preventive actions within the quality system to prevent recurrence.
  • Perform other related duties as assigned to support departmental objectives and organizational priorities.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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