It is our pleasure to be working with a global medical device manufacturer, who due to internal progression is currently seeking a dynamic and commercially minded Regulatory Affairs professional to join their global regulatory team.

This role will provide specialist regulatory expertise in the research development and marketing of our client’s products to ensure that regulatory approvals are obtained and maintained in accordance with the agreed registration programme and the needs of the business plans.

In addition to this it will be responsible for providing strategic direction and support across a specific business unit covering all of their regions including APAC.

To be considered for this excellent opportunity you will need to be degree education with a minimum of 5 years regulatory experience within the medical device sector.

Due to the wide geography reach of this role, prior regulatory exposure and knowledge of regulatory requirements covering Europe, USA and some countries in APAC such as Japan and China is essential.

This is an excellent opportunity to join a well established, driven organisation in a position that will have a significant impact on the success and further development of the organisation.