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.