L

Lyrebird Health

Automates patient documentation for clinicians

QA Manager

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMelbourne VIC, AustraliaNo salary listedHybrid

About the Job

Requirements

  • Deep experience applying quality and regulatory requirements to medical devices, Software as a Medical Device (SaMD), or diagnostics inside product development teams.
  • Working knowledge of ISO 13485 and ISO 14971, and the judgment to interpret them for a software product.
  • A track record of leading internal or external audits and quality system initiatives through to a clean result.
  • Experience owning an electronic Quality Management System (eQMS) end to end, including implementation, governance, training, document control, continuous improvement, and management of Technical Files, Design History Records, and post-market records within it.
  • Experience managing quality across the full product lifecycle, including design and development controls, risk management, post-market activities, and regulatory change assessments.

Responsibilities

  • Own the path to ISO 13485 certification in H1 2027, from readiness planning through to a successful certification audit.
  • Take ownership of the Quality Manual and make it something the business actually runs on.
  • Ensure every process documented in the eQMS has clear accountability for ongoing maintenance, document control, and governance that stands up to an auditor's scrutiny.
  • Design and implement post-market surveillance fit for a Software as a Medical Device product that updates at software speed.
  • Lead the first Management Review with senior leadership, setting the rhythm for how quality is reported and decided on at the top.
  • Run internal self-audits ahead of certification, identifying gaps before an external auditor does.
  • Embed design controls and risk management into engineering and clinical team workflows so quality is designed in rather than bolted on.

Desired Qualifications

  • Working knowledge of IEC 62304 and medical device cybersecurity requirements.
  • Start-up or scale-up experience solving complex quality and regulatory problems laterally.
  • Experience running a Quality Management System across more than one jurisdiction.

About the Company

Lyrebird Health

Automates patient documentation for clinicians

Lyrebird Health builds tools to automatically generate medical documentation, freeing clinicians from hours of typing so they can focus on the patient. It creates patient notes and other relevant clinical documents without requiring manual data entry, enabling clinicians to listen more closely during visits. This product differentiates itself by targeting providers who prioritize high-quality patient care and by removing administrative friction that disrupts the patient encounter. The overall goal is to improve the quality of care by reducing writing overhead and letting clinicians devote more time to the patient.

Company size
51-200
Company stage
Series A
Total funding
$7.8M
Headquarters
Melbourne VIC, Australia
Founded
2023

Recently Posted Jobs

Explore more opportunities at Lyrebird Health

See more jobs