Veryan Medical is entering an exciting period of growth, having obtained FDA approval for our product in the US in October 2018, followed by our acquisition in December 2018 by Otsuka Medical Devices UK Ltd.
This has opened up new career opportunities and we are looking for additional team members to join us as we start new projects to expand the indications for use of our unique BioMimics 3D stent and further develop our product range.
We are currently recruiting for the following full-time vacancies. To apply, please send your CV and a covering email to: email@example.com
Senior DA Engineer/DA Engineer, Galway
Vacancy ref: V104
You will be working as part of the development teams in the development of Veryan’s new stent platforms. Working predominantly on projects to introduce or improve products for treatment of a range of peripheral arterial disease states. Design Assurance is integrated with the Product Development process. The Design Assurance Engineer will support the Company’s product development and commercialisation strategy. More…
Senior Quality Engineer, Galway
Vacancy ref: V097
As part of our plans for growth, we are looking for a Senior Quality Engineer. Your role will be to support the Quality Manager in ensuring that all product released by Veryan for human use meets the Company’s product quality requirements, and to ensure that product is manufactured, released and distributed in accordance with regulatory requirements. More…Senior QA Engineer
RA Manager, Galway
Vacancy ref: V065
As RA Manager, you will be responsible for the management of the company’s regulatory affairs, playing an active role in developing regulatory strategies for new products and ensuring maintenance of existing global regulatory approvals. More… RA Manager
Senior Regulatory Affairs Consultant, Galway
Vacancy ref: V103
We are looking for a contractor to join the team for 6-9 months to cover the increased workload as new projects come on stream, and to cover for planned staff leave. In this role, you will be responsible for the management of the company’s regulatory affairs activities. More…