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Senior R&D Program Manager

ID
15197
Location
Galway, Ireland
Role Type
Permanent
Contact
Dee Curley
Email
dee@hero.ie
Phone
+353867902191
LinkedIn
click here

Recruitment Consultant

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Senior R&D Program Manager

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Senior R&D Program Manager 

Location: Galway, Ireland Hybrid

Our leading medical device client is seeking a Senior R&D Program Manager to join their team in Galway. This is an exciting opportunity to work on innovative technologies in Pulse Field Ablation (PFA), contributing to the next generation of life-saving medical devices.

In this role, you will act as a cross-functional leader, accountable for driving decision-making and execution across development projects. You will oversee the full product development lifecycle – from building high-performing teams through to ensuring the successful delivery of commercial solutions. Collaboration is key: you’ll work closely with functional and regional leaders, championing innovation, empowerment, and cross-functional effectiveness.

This is more than a job – it’s an opportunity to make a lasting impact on patient outcomes worldwide.


Key Responsibilities

  • Drive cross-functional core teams and partner with functional leaders to ensure clarity of program objectives, deliverables, and key milestones.

  • Lead projects to successful completion – on time, within budget, and in scope – while managing stakeholder expectations.

  • Own program budgets and schedules, ensuring alignment with business priorities.

  • Apply critical thinking and problem-solving skills to scope definition, cost control, scheduling, and risk management.

  • Present program updates and outcomes to leadership teams.

  • Mentor and engage team members to maximise contribution and project success.

  • Champion best practices in product development, including Voice of Customer, early risk mitigation, and Design for Reliability and Manufacturability (DRM).

  • Travel up to 25% (domestic).


Key Skills & Experience

  • Bachelor’s degree in a technical discipline with a minimum of 7 years of relevant experience, or advanced degree with 5+ years’ experience.

Preferred Qualifications:

  • Advanced degree such as MS or MBA.

  • Experience in the medical device industry, particularly in new product development, released product management, clinical trials, and regulatory submissions.

  • DRM Blackbelt certification.

  • Proven success managing complex, cross-functional project teams.

  • Strong leadership skills within a diverse, global, matrixed organisation.


What’s on Offer

  • Competitive salary and comprehensive benefits package.

  • Opportunity to work on cutting-edge medical technologies with a global impact.

  • Collaborative and empowering work environment with career growth opportunities.

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