Senior Regulatory Affairs Associate

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Finding Outstanding Talent in the Emerging Scientific Industry

Regulatory Affairs Team Lead

IVD

Edinburgh

I am very pleased to be able to offer this role with one of our established clients. 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! They recently received impressive funding for a new product and are taking over the cutting edge diagnostics space.

This role will be leading a small team across new products and continuing surveillance for one of their most successful product portfolios.

Key Requirements:

• UK, EU and US regulatory submission experience is ideal but we can consider individual merit
• Experience leading 510(k) submissions would be ideal
• Experience in CE marking, PMS activities for global diagnostics
• A people orientated personality / previous team lead experience

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, hybrid in one of the UK's best cities!
• 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

Seniority level

• Seniority level
• Associate

Employment type

• Employment type
• Full-time

Job function

• Job function
• Writing/Editing and Quality Assurance
• Industries
• Medical Equipment Manufacturing and Pharmaceutical Manufacturing

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