Medical Device Project Manager

Actalent

Dublin

On-site

EUR 70,000 - 110,000

Full time

42 hours ago
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Job summary

Actalent is seeking a Device Engineering Project Manager in Dublin to lead development and improvement of medical devices. You will coordinate cross-functional teams across engineering, clinical, regulatory and operations to ensure quality, regulatory compliance, and on-time delivery.

The ideal candidate has an engineering degree (or Master's) with 5+ years in medical device development or project management, plus strong knowledge of FDA/ISO regulations and excellent stakeholder management

Qualifications

  • This candidate holds a degree in engineering or a technical field.
  • Has 5+ years in medical device development or project management.
  • Knowledge of FDA and ISO regulations is required.
  • Experience with complex electromechanical or disposable devices.
  • Excellent communication and stakeholder management skills.

Responsibilities

  • Lead the development and improvement of medical devices.
  • Manage cross-functional teams across engineering, clinical, regulatory and operations.
  • Ensure projects meet quality, regulatory, and timeline expectations.
  • Drive technical project execution and delivery.
  • Collaborate with internal and external stakeholders to align goals.

Skills

Engineering degree
Master's in engineering
Strong communication
Stakeholder management

Education

Engineering degree
Master's in engineering

Job description

I'm working with a global leading pharmaceutical company that’s currently seeking a Device Engineering Project Manager based in Dublin.

This role involves leading the development and improvement of medical devices, managing cross-functional teams, and ensuring projects meet quality, regulatory, and timeline expectations. You’ll be at the center of technical project execution, collaborating with engineering, clinical, regulatory, and operations teams.

The ideal candidate will have:
  • A degree (or master’s) in engineering or a technical field
  • 5+ years of experience in medical device development or project management
  • Strong knowledge of FDA and ISO regulations
  • Experience with complex electromechanical or disposable medical devices
  • Excellent communication and stakeholder management skills
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