Junior Regulatory Affairs Specialist
Limbic
- London
- £35,000 per year
- Permanent
- Full-time
- 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
- Salary = £35,000 + stock options
- Limbic is a remote-first company, but alignment with core UK hours is required
- Reporting into US General Manager
- 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
- Flexibility regarding fully remote, from our central London office or hybrid
- Twice a year company wide meet-ups in Europe
- 25 days PTO
- Paid maternity, paternity, parental leave packages
- Equity share options
- Quarterly ‘life’ days
- Access to mental health support