Capital Projects Facilities Lead

Medtronic

Northern (KY)

On-site

USD 90,000 - 140,000

Full time

2 days ago
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Job summary

Medtronic plc is seeking a Facilities Program Manager to lead capital projects from planning through commissioning and closeout, onsite at the Villalba Facility in Puerto Rico. You will partner with diverse teams to deliver projects safely, on schedule, and within budget, while ensuring regulatory compliance and alignment with business objectives.

The role requires strong financial acumen, PMP/PE is preferred, and experience in med-tech/pharma environments with ISO13485;

Qualifications

  • Bachelor’s Degree and 5+ years of Facilities Program Management experience.
  • Experience managing capital projects and programs.
  • PMP or PE Certification preferred.
  • OSHA 30 Hour or equivalent safety certification.
  • Experience with ISO13485 quality management system.
  • Procore/Bluebeam/AutoCAD/BIM experience.

Responsibilities

  • Lead projects through the entire project lifecycle from planning to closeout.
  • Direct remote & local teams to ensure alignment and timely delivery.
  • Manage external design consultants, construction managers, contractors, and service providers.
  • Develop project business cases, manage capital budgets, risk assessment, and forecast expenditures.
  • Coordinate with cross-functional stakeholders to ensure regulatory compliance and quality standards.
  • Travel 25-50%.

Skills

Project management
Cross-functional collaboration
Financial acumen
Communication

Education

Bachelor's Degree
Master's Degree

Tools

Procore
Bluebeam
AutoCAD
BIM

Job description

Medtronic plc is seeking a Facilities Program Manager to lead capital projects from planning through commissioning and closeout, onsite at the Villalba Facility in Puerto Rico. You will partner with diverse teams to deliver projects safely, on schedule, and within budget, while ensuring regulatory compliance and alignment with business objectives.

The role requires strong financial acumen, PMP/PE is preferred, and experience in med-tech/pharma environments with ISO13485;

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