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Quality Project Manager

Are you ready to take your career to the next level? As a Quality Project Manager, you won't just be part of the team – you'll be at the forefront, leading the way in quality and compliance while showcasing your exceptional project management skills. If you're passionate about making an impact and thrive in a dynamic, regulated environment, we want to hear from you!

Key Roles & Responsibilities:

  • Provide leadership, standardization and implementation of best practice for project management within the EUMDR site team

  • Provide Quality and Compliance expertise and facilitate Project planning, to support implementation activity

  • Ensure regulatory compliance to GMP’s of all medical device regulatory agencies (e.g., FDA, ISO, and MDD)

  • Liaise with product support teams, R&D and regulatory on component quality issues and supplier initiatives.

  • Liaise with quality, engineering, R&D, Labelling and regulatory accountable persons both internal to the plant and externally within the corporation.

  • Lead resolution of problems that impede project progress.

  • Responsible for other projects as assigned by the company.

  • Deliver project status updates to senior management and project sponsors incorporating status reports and project plan updates.

Education & Experience:

  • BSC Science or Engineering degree with 5 or more years within a highly regulated medical device or pharmaceutical environment with proven project management skills (or Equivalent)

  • Experience in an MDD, FDA, ISO, GMP regulated environment.

  • Strong team member with the ability to identify and drive regulatory compliance improvements.

  • Good administrative/organizational ability with excellent attention to detail.

For a confidential discussion and more information on the role, please contact Aisling Lane.

(021) 4320675