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Validation Engineer

  • Location: County Westmeath
  • Job Type:Permanent
  • Sector: Engineering
  • Contact Email:
  • Client: Teleflex
  • Job Ref: 21809

We have an opening for a Validation Engineer with a Leading Global Medical Device company based in Athlone. The Sustaining Engineer will be responsible for for assisting and supporting the execution and oversight of Sustaining Engineering material CIP (Cost Improvement Projects) within the Global Procurement Team.

The Validation Engineer is required to have an understanding of development, manufacturing, Design Control, medical device regulation, and project management. This is Permanent role with a Hybrid Working Option for the succesful candidate.

Job Responsibilties:

  • Draft and route project Charters, identifying the required deliverables per local and global procedures, as well as governing regulations, with moderate guidance.

  • Interface with cross functional teams to track project deliverables, responsibility, and progress.

  • Utilize available data to build timelines, task trackers, risk registers, meeting cadences, etc. based on basic knowledge of project management processes.

  • Actively coordinate and manage the portfolio of projects to be delivered and as agreed by the senior leadership team as priority projects. 

  • Assist program leaders and individual contributors in directing and managing a project’s development from concept to project completion.

  • Help define project scope, goals and deliverables that support business objectives in collaboration with senior management and stakeholders.

  • Ensure that full-scale project plans and associated communication documents are fully prepared to support program deliverable.

  • Work with project leaders to estimate the resources and participants needed to achieve project goals.

  • Oversee the planning and scheduling of project timelines and milestones using appropriate tools.

  • Define individual project success criteria and disseminate them to involved parties throughout project life cycle.

Job Requirements:

  • Bachelor of Science in an Engineering or related technical discipline.

  • Min 3 years of experience in medical device, regulated industry, or related field.

  • Has basic understanding of development and manufacturing processes.

  • Is able to utilize available data to build timelines, task trackers, risk registers, meeting cadences, etc. 

  • Strong Communication Skills.

  • Ability to handle multiple tasks and to prioritize/schedule work to meet project needs with routine supervision. • Experience with Microsoft Office – PC, Word, Excel, PowerPoint.

If you would like more information on this role you can contact Paul Dunican

(090) 641 7022