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JOB DETAILS

Head of QARA

CompanyReset Health
LocationLondon
Work ModeOn Site
PostedNovember 14, 2026
About The Company
Helping patients manage obesity and Type 2 diabetes with our Roczen app. Our team of specialist clinicians combine personalised care with innovative weight-loss therapies. We integrate diagnostics, bespoke diet and lifestyle plans, prescription-only medications, 1:1 clinical care, dedicated mentors and community support all in one easy-to-use digital platform.
About the Role

Reset Health are looking for a Head of Quality Assurance and Regulatory Affairs (QARA) to own our regulatory strategy and build our quality function.

Reset Health is the Therapeutic Optimisation Company. The future of healthcare is not just about creating better medicines. It is about achieving the best possible outcome from every medicine, for every patient.

You’ll be our first dedicated QARA hire, with the chance to shape quality and regulatory affairs at a fast-growing health tech company. You’ll run the Quality Management System (QMS) day to day, provide hands-on leadership through audits, and ensure our path to market is clear, sustainable and grounded in patient safety. Your first big milestones will be taking full ownership of our regulatory work and setting a clear route to market for our AI-driven Software as a Medical Device (SaMD) products.

Roles & Responsibilities
  • Own our regulatory strategy and routes to market via EU MDR and FDA.
  • Act as our PRRC and main contact for Notified Bodies and health authorities.
  • Maintain ISO compliance across our QMS, partnering with our Governance Lead, and lead the move to an eQMS when needed.
  • Embed ISO 13485, IEC 62304 and ISO 14971 into the product lifecycle with Product, Engineering and Clinical teams.
  • Lead preparation for certification and surveillance audits.
  • Run day-to-day quality: Technical Files, DHF, post-market surveillance, CAPA, supplier and risk management.

Essential

  • A track record of leading digital health or SaMD products through regulatory approval and ISO 13485 certification.
  • Strong technical expertise in ISO 13485 and IEC 62304, and experience setting regulatory strategy.
  • A hands-on approach and a love of getting into the detail.
  • The ability to build trusted relationships with senior colleagues across functions and with Notified Bodies.
  • Eligibility to act as PRRC under EU MDR requirements.

Desirable

  • Experience leading AI as a Medical Device (AIaMD) products through regulatory approval.
  • Experience using AI tools to speed up development and documentation.
  • Experience leading organisational change, including implementing an eQMS, while keeping product delivery on track.
  • Experience moving teams from an external regulatory consultancy model to in-house operational ownership.

If you meet most of the requirements but not all, we’d still encourage you to apply. Great QA/RA professionals come from many different backgrounds and career paths, and we want our team to reflect that. If you need any adjustments during the application process, just let us know.

What we offer

  • Competitive salary of £80,000-£90,000 per annum, depending on experience
  • Opportunities to build skills and progress within a growing digital health organisation
  • Private medical insurance
  • Enhanced parental leave
  • Enhanced sick leave
  • Pension scheme

To apply, please send your CV along with a short note explaining how you meet the requirements and why you would like to join Reset Health. Interviews will be held on a rolling basis.

Key Skills
Regulatory strategyQuality management systemISO 13485IEC 62304ISO 14971SaMDEU MDRFDAPRRCTechnical filesPost-market surveillanceCAPARisk managementDigital healthAIaMD
Categories
HealthcareTechnologyManagement & LeadershipEngineeringSoftware
Benefits
Private medical insuranceEnhanced parental leaveEnhanced sick leavePension scheme
Job Information
📋Core Responsibilities
The Head of QARA will own the regulatory strategy and build the quality function, including managing the Quality Management System (QMS). They will act as the PRRC and lead the company's path to market for AI-driven Software as a Medical Device (SaMD) products.
📋Job Type
full time
💰Salary Range
£80,000 - £90,000
📊Experience Level
10+
💼Company Size
65
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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