Job Description
A Class i Medical Device manufacturer are hiring a Group Regulatory Lead.
It’s a predominantly remote role where you’ll get the autonomy to do things your way.
You will act as the group's regulatory subject matter expert, responsible for ensuring that all new and existing products meet applicable regulatory and safety requirements in all target markets across multiple sites.
You will guide teams on standards, risk management, technical documentation, and product safety, while rationalising and maintaining technical files.
There are five UK sites, all with their own quirks, some are doing things well, others need a bit more guidance. It’s all about having the character to educate, rather than police.
What you need to know:
💻 Mostly remote (you’ll barely leave your home office)
💰 £55–65k depending on experience
🩺 Private medical + pension
👤 This is a stand alone RA role, with scope to hire once you’re settled (1-2 hires)
What skills we need to see:
1. 5-10 years’ regulatory experience in medical device design & manufacture, minimum Class I, Class IIA would be advantageous.
2. Experience of working in a manufacturing environment in accordance with the requirements o...