As a seasoned Program Manager, you have the opportunity to drive innovation in interventional cardiology by leading a cutting-edge product development program from concept to commercialization.
The position is based in Galway and offers the chance to contribute directly to the success of a pioneering technology in the cardiovascular space.
You will play a key role in driving a novel cardiac support device through development, working cross-functionally with engineering, clinical, regulatory, and commercial teams.
This is a dynamic and agile environment that requires strong project management skills, including establishing robust project plans and timelines, ensuring program delivery on time, and implementing structured engineering review processes to minimize design risks.
In addition to these responsibilities, you will coordinate workstream activities, prioritize critical path tasks, communicate clearly with internal and external stakeholders regarding project progress and risks, and anticipate potential issues and develop effective mitigation strategies.
A Master's Degree in Biomedical Engineering or a related discipline is required, as well as minimum 10 years' experience in medical device development, ideally in cardiovascular or interventional cardiology. Proven track record in program management within a regulated environment is also essential.
Key Responsibilities:
* Lead the execution of the full product development program from concept to manufacturing and scale-up in a regulated environment.
* Establish and manage robust project plans and timelines; ensure program delivery on time.
* Implement structured engineering review processes to minimize design risks.
* Coordinate workstream activities and ensure prioritization of critical path tasks.
* Communicate clearly with all internal and external stakeholders regarding project progress and risks.
* Anticipate potential issues and develop effective mitigation strategies.
Candidate Profile:
* Master's Degree in Biomedical Engineering or a related discipline (or equivalent industry experience).
* Minimum 10 years' experience in medical device development, ideally in cardiovascular or interventional cardiology.
* Proven track record in program management within a regulated environment.