Regulatory Affairs Associate

Description:

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