Senior Project Manager, Medical Devices — Durham (On-site)

GILERO; Chicago (IL); On-site; USD 120,000 - 150,000; Full time

Job summary

Gilero seeks an experienced Senior Project Manager to lead design and development projects in medical devices across multiple sites. You will drive projects from concept to commercialization, ensuring on-time, on-budget delivery with quality and regulatory compliance.

The role involves coordinating cross-functional teams, vendors, and client communications. Ideal candidates have 8+ years in PM for medical devices, a BS in engineering, PMP preferred, and strong writing and data-analysis skills.

Qualifications

• BS in Engineering or 4-year technical degree.
• PMP Certification (preferred).
• Experience: 8+ years with 5+ years as a Project Manager in Medical Devices.
• Knowledge of medical device regulations (FDA/ISO).
• Strong project management skills; able to work independently or in teams.

Responsibilities

• Organize project activities, lead the project team, and manage timelines within budget.
• Lead multi-year medical and drug delivery development projects including electronic and disposable devices.
• Forecast engineering resources for short/mid/long-term needs.
• Generate financial and project reports for internal and external communication.
• Coordinate vendor activities with suppliers and labs.
• Maintain project documentation and ensure deliverables meet customer expectations.
• Mentor junior project managers and support recruiting for PM roles.
• Support PM objectives company-wide and participate in client updates.

Skills

Project management

Engineering

Client relations

PMP

FDA/ISO knowledge

Communication

Data analysis

Microsoft Excel

Documentation

Education

BS in Engineering or 4-year technical degree

Tools

Excel

Word

Job description

Gilero seeks an experienced Senior Project Manager to lead design and development projects in medical devices across multiple sites. You will drive projects from concept to commercialization, ensuring on-time, on-budget delivery with quality and regulatory compliance.

The role involves coordinating cross-functional teams, vendors, and client communications. Ideal candidates have 8+ years in PM for medical devices, a BS in engineering, PMP preferred, and strong writing and data-analysis skills.