Job title:Sr Program Manager
Location: Ballybrit Upper Industrial Estate, Galway
Benefits:Top salary, Pension, healthcare, yearly bonus, 4 day week.


Client:
My client are the global expert in the design, development, and manufacturing of complex medical devices and component technologies



Role overview:
In your role as a Senior Program Manager you will direct the multi-phase product development process of medical devices and components from concept through market introduction and transfer to manufacturing. You will manage projects contracted by client companies and/or internal development and improvement projects. Your responsibility as Senior Program Manager is managing cross-functional teams to accomplish project goals on budget, on schedule, and in-scope.

As a member of our team, you will have the opportunity to work in a dynamic and collaborative environment, where your ideas and contributions will be valued and respected.



Responsibilities:

• Serves as the client’s primary point of contact into Nordson MEDICAL for all project-related matters;
• Directs day-to-day activities for multiple project teams through managing project plans, resources, status reporting, issue resolution, risk management, and accountability for deliverables;
• Manages complex projects or programs of multiple interrelated projects;
• Responsible for leading cross-functional teams to support projects from Research & Development and into New Product Introduction;
• Lead projects for continuous improvement, capacity expansion, or transfer of existing manufacturing lines;
• Develops, improves, and uses PM best practice tools (Timelines, Project schedules, RAID documents, meeting minutes, 4-panels, etc.) to facilitate information flow between team members, the project leader, management, and the client.

• Bachelor's degree required; Master’s degree preferred. Degree focus in Mechanical or Biomedical Engineering is desired;
• Minimum of 5-7 years of experience in program management or Project Management Professional (PMP®) certification;
• Proficient knowledge of FDA QSR and ISO 13485 medical device regulations
• Demonstrated professional communication skills through both verbal and written means regarding project and technical matters