Medical Devices Programme Manager with previous experience working within a highly regulated Medical Device environment is required by innovative market leader in Galway.
In this role, you will be responsible for Programme Management of Product and Process Development projects: manage key projects – ensuring they are properly resourced, that adequate documentation is maintained, that risks are identified & highlighted, that project members are lead and managed and that stakeholders are regularly updated on progress.
The successful candidate will have a BSc. in Engineering and at least 8 years’ experience in a Project Management role within in a Medical regulated Development or Manufacturing environment, with experience working with ISO 13485 and FDA Design and Development processes. It is also expected that you will have strong Technical Leadership and Project Management experience, experience with project planning methodologies and knowledge of Design Verification and Process Validations.
If you would like to hear more, please forward your cv to Emer Moore and we can arrange a call to discuss this role in confidence