Design Quality Engineer
Heidi Health · London · AU
Posted 60+ days ago
Regulatory Affairs
Hybrid
Not yet analysed
Demand80
Career growth75
Healthcare fit70
Remote potential60
5-year outlook
Salaries for regulatory/quality engineers in health tech are competitive and likely to grow as medical software regulations tighten. Expect above-average compensation for experienced candidates, with potential for leadership roles.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-08-26
Intelligence details
Why this is worth applying to
Clinicians with a technical bent and interest in regulatory affairs should consider this role as a bridge into health tech compliance. However, it requires specific standards knowledge, so upskilling in IEC/ISO frameworks is essential.
Who should apply
Doctors, nurses, or allied health professionals with informatics experience, familiarity with EHRs, and a passion for patient safety and quality improvement, who are willing to learn medical device regulations.
CV angle
Highlight clinical experience as evidence of understanding user needs, patient safety, and documentation rigor. Emphasize any involvement in quality improvement, risk assessment, or technology adoption in clinical settings.
Skills to highlight
- Knowledge of medical device standards
- Risk management
- Design control
- Agile development
- Communication
- Attention to detail
- Clinical workflow understanding
Role summary
A Design Quality Engineer at Heidi Health ensures that their AI scribe software complies with global medical device standards (IEC 62304, ISO 14971, ISO 13485) by implementing design control processes and supporting audits, bridging engineering and regulatory affairs.
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