QARA Software Engineer - Medical Devices, Onsite 4x/wk in Comberton

QARA Software Engineer - Medical Devices, Onsite 4x/wk in Comberton

Comberton Full-Time 35000 - 45000 £ / year (est.) No working from home possible
Foundation Partners

At a Glance

  • Tasks: Lead quality and regulatory initiatives for medical device development.
  • Company: Flok Health, a forward-thinking company in the medical device sector.
  • Benefits: Competitive salary, hands-on experience, and a chance to shape industry standards.
  • Other info: Onsite role in Cambridgeshire, fostering collaboration and innovation.
  • Why this job: Make a real difference in healthcare by developing user-centric medical devices.
  • Qualifications: Engineering background with a focus on quality and regulatory processes.

The predicted salary is between 35000 - 45000 £ per year.

Flok Health is seeking a QARA Engineer to take ownership of quality and regulatory initiatives.

You will apply an engineering approach to build tools and processes that support medical device development, with close collaboration across clinical, product and engineering teams.

The role emphasizes user‑centric design and practical application of ISO standards.

This is an in‑office role four days a week in Cambridgeshire, with opportunity to shape regulatory workflows and device documentation.

#J-18808-Ljbffr

QARA Software Engineer - Medical Devices, Onsite 4x/wk in Comberton employer: Foundation Partners

Foundation Partners is an exceptional employer that prioritises employee engagement and development within a vibrant work culture. With a competitive salary range of £40,000 to £50,000 per annum, employees benefit from valuable perks and opportunities for professional growth, making it an ideal place for those passionate about shaping HR operations and supporting diverse clients.

Foundation Partners

Contact Details:

Foundation Partners Recruitment Team

We think you need these skills to ace QARA Software Engineer - Medical Devices, Onsite 4x/wk in Comberton

Quality Assurance
Regulatory Compliance
ISO Standards
User-Centric Design
Medical Device Development
Collaboration Skills
Process Improvement