Regulation & Quality Lead
PhysitrackLondon, England, United Kingdom
Posted November 11, 2025
60000 - 75000 EUR year
Full Time
About the Company
Physitrack’s mission is to elevate the world’s wellbeing with our groundbreaking digital healthcare and employee wellbeing tools.
Job Description
Physitrack is seeking a Regulation & Quality Lead to prepare the organisation for MDR/UKCA certification. The ideal candidate will have experience with Quality Management Systems (ISO 13485 / ISO 9001), Medical Device Software (SaMD), or Regulatory Compliance in a digital health or wellness environment.
Requirements
- Bachelor’s degree, preferably in a technical, scientific, or regulatory discipline.
- Proven experience working in healthcare, wellness, medtech, or a digital product company.
- Practical experience with one or more of the following: Quality Management Systems (ISO 13485 / ISO 9001), Medical Device compliance (MDR, UKCA, FDA 21 CFR Part 820), Software lifecycle & validation (IEC 62304)
- Fluency in using AI-based tools for decision and workflow support, as well as document and AI-powered presentation creation tools.
- Excellent written and verbal communication skills.
- Pragmatic, detail-oriented, and commercially aware.
Benefits
- Competitive salary based on experience, up to 75,000 EUR full time per annum
- Remote work within the EU or from our London office if UK based
