Job title: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 clients 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. Skills and Qualifications: Bachelor's degree required; Masters 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 Does this sound like your next career move? For more info forward your application or contact me on OR Benefits: Bonus, pension, healthcare, 4 day week