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I am partnering with a leading global company in the medical device industry to find a highly motivated and experienced Project Manager to join their team based here in Galway.
The Role:
As the Project Manager, you will play an integral part in sustaining projects within the Structural Heart Valve franchise. Scope of projects includes all product support activities as it pertains to the Acurate Aortic System from initial launch to product end of life across business units and manufacturing sites.
Projects will range from small one-off tasks to large process improvement, design change, design transfers, line extensions, and projects/Corporate initiatives driving global productivity.
Responsibilities:
* Leads and manages the development and implementation process of the company's products, processes, and services involving departmental or cross-functional teams focused on the delivery of existing products/services.
* Champions and leads significant and complex new product development, post-commercialization, and continuous improvement initiatives; may be responsible for managing high-priority projects.
* Lead cross-functional teams and manage multiple projects from small to large scope, including Schedule, Scope, Costs, and Resources.
* Required to travel internationally an estimated 50% of the time.
Project/Program Management:
* Develops and implements overall project plan, including cost, schedule, risk, and performance and monitors progress against business key objectives and goals.
* Identify prioritization and resources required for assigned projects and activities with supporting cross-functions.
* Identify, communicate, and manage technical challenges and business risks.
* Drive and influence results by acting with speed, agility, and adaptability, assigning clear authority and accountability while integrating and aligning efforts across functional areas, business units, and/or geographies in order to achieve goals.
* Monitors and ensures compliance with company policies and procedures (e.g., compliance with FDA, DEKRA regulations).
* Provides structured thinking to the project team on overall approach and delegates as appropriate.
* Leads the team in appropriate decision-making through strong judgment and the ability to analyze options and implications.
* Investigate and develop approach/solution to address technical problems with project teams.
* Provide timely communication on project progress updates to all relevant cross-functions and levels within the organization, including presentations to senior leadership.
Requirements:
* Min. HETAC level 8 in Engineering: electrical, mechanical, industrial, software, manufacturing; a Master’s in Project Management would be preferred.
* 4+ years of project management experience.
* Experience with the development of medical devices is a plus.
* Strong experience in project managing significant new product activities that require collaboration with Divisional R&D, Program Management, Regulatory Affairs, Design Assurance, Process Development, Sustaining Engineering, and Operations.
* Proven leadership skills in change management and project management.
* Demonstrates excellent verbal and written communications to project team and all stakeholders.
* Must be strong in people management and team building.
* Must be proficient with MS Project.
* Portuguese language skills will be an advantage.
* You may be required to travel regularly to other sites up to 50%, and the length may vary depending on work content.
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