Limbic is making mental healthcare available to everyone, everywhere.
Limbic’s vision is to ensure the highest quality therapy is accessible to everyone, everywhere. The way we do that is by deploying AI responsibly, using it to augment clinical care and reduce barriers to accessing therapy at scale. Limbic is already used in over 30% of Talking Therapies in the NHS and is deemed safe and effective after successfully gaining UKCA Class IIa certification, the only AI mental health decision support tool to do so.
As a Junior Regulatory Affairs Specialist, you’ll be joining a growing Compliance and Regulatory department operating at the forefront of AI, software and medical devices in mental health. You will take ownership of Limbic’s quality management system and will work cross departmentally to ensure Limbic retains its position as the most accredited and trusted mental health technology on the market.
What you’ll be doing at Limbic:
Managing Limbic’s quality management system, from the day-to-day procedures to auditing, training and monitoring
Iterating on and improving our QMS processes as the company scales
Supporting on medical device certifications, audits, file updates and core SaMD process development to continue Limbic’s precedent as a highly accredited mental health AI company
Serving as our compliance champion working closely with our mental health services and cross-functionally with research, AI, product and growth internal teams to embed our compliance principles at the heart of everything we do
Keeping up to date with relevant legislation, methodologies, standards and appropriate regulatory frameworks to keep Limbic at the cutting edge of AI, software, medical devices and mental health
Job Details:
Salary = £35,000 + stock options
Limbic is a remote-first company, but alignment with core UK hours is required
Reporting into US General Manager
Requirements
Who you are:
Detail oriented with experience in compliance processes of auditing, reviews and continuous improvement
First hand experience of ISO 13485 and UK MDR, preferably in the context of software devices and healthcare
Highly organised, able to create clear project plans, juggle priorities and drive work forward cross-functionally
Self-starter with a strong sense of ownership, adaptability, and a willingness to take on new challenges
Comfortable with uncertainty and the unknown
Your default is to use data to problem solve and craft scalable compliance systems
Benefits
Flexibility regarding fully remote, from our central London office or hybrid
We take employee wellbeing seriously at Limbic and in addition to the above we offer:
Quarterly ‘life’ days
Access to mental health support
About Limbic:
Limbic is making mental healthcare available to everyone, everywhere. We're growing quickly and we're backed by top-tier investors, as well as Innovate UK, Digital Health London, Entrepreneur First, and the European Commission.
It’s challenging. We’re ambitious. And we’re supporting one another to achieve our best and make real impact in the world.
Find out what Limbican's think about the working culture here.
Your CV has been submitted successfully.
Complete form below to directly Send your CV / Linkedin Profile to Junior Regulatory Affairs Specialist at Limbic.
@
You will receive all responses from employer on this email
Example: Application for the post of 'Accountant'
Example: Introduce your self and give purpose of your application