Senior Project Manager, Medical Device R&D (Hybrid)

Cook Medical Incorporated; Limerick; Hybrid; EUR 90,000 - 120,000; Full time

Benefits offered by this job

Hybrid Work Model

Medical Health Insurance cover for you

Job summary

Cook Medical Incorporated in Limerick is seeking a Senior Project Manager, Research and Development, to lead project management efforts for medical device development from concept through to market.

Reporting to the Manager, Research and Development, you will coordinate with technical leads, manage budgets and milestones, mentor direct reports, and ensure compliance with Quality, Regulatory and ISO/EU/FDA standards while driving cross-functional collaboration.

Qualifications

• Bachelor’s degree required, preferably in engineering or a related field.
• Minimum of 5 years’ relevant project management experience.
• Certified in Project management is essential.
• Agile methodology is preferred but not essential.
• Knowledge of ISO, EU, FDA medical device standards.
• Willingness to travel for company business.

Responsibilities

• Lead project management for R&D projects from concept to market launch.
• Coordinate with technical leads to progress projects and manage milestones.
• Establish and manage routine team meetings for plan updates and issue resolution.
• Maintain oversight of project budgets and risks; develop mitigations.
• Communicate project status to stakeholders and senior management.
• Foster cross-functional collaboration and vendor coordination.

Skills

Project management

Leadership

Communication

Problem-solving

Strategic thinking

Mentoring

Education

Bachelor’s degree in engineering or related field

Tools

MS PowerPoint

Job description

Cook Medical Incorporated in Limerick is seeking a Senior Project Manager, Research and Development, to lead project management efforts for medical device development from concept through to market.

Reporting to the Manager, Research and Development, you will coordinate with technical leads, manage budgets and milestones, mentor direct reports, and ensure compliance with Quality, Regulatory and ISO/EU/FDA standards while driving cross-functional collaboration.