Regulatory Affairs Associate

Job Description

Regulatory Affairs Associate
IVD
Edinburgh

I am very pleased to be able to offer this role with one of our established clients, responsible for manufacturing various successful IVD products. With a global presence and several large sites, this is a great opportunity to take your regulatory experience global and work within the UK, EU, APAC and US markets!

Main Responsibilities: -
Compile and assist with global regulatory submissions including 510(k) submissions
Complete product labelling tasks
Liaise with external and internal stakeholders including competent authorities
Conduct process improvements projects within the team

Key Requirements: -
Experience within IVD Regulatory Affairs is essential
A communicative personality is beneficial
Experience in global markets is also beneficial

Why Apply?
No doubt the diagnostics world has been shaken after the COVID-19 situation, but on offer is a stable position, with a business who have been operating for 17 years. They now have over 300 employees across multiple sites and a successful product portfolio.
A flexible working model
What the team describe as a positive, supportive culture with on-site facilities, regular social incentives if you want to partake, and health and wellbeing initiatives.

Apply now by hitting 'easy apply' or emailing [email protected]