Join Genomic Diagnostics, the national genomics service for Healius Pathology, and work at the cutting edge of clinical genomics in inherited disease.

This is an opportunity for a senior subject matter expert to shape how we respond to growing test volumes and evolve our genomics services through new technologies, automation and digital tools. What makes this role stand out is the opportunity to leverage your leadership, technical and clinical skills to play a key role in advancing our genomic testing capabilities.

If you’re a senior or clinical scientist looking to step into a leadership position, this is a role for you You’ll be part of a collaborative and supportive environment where your expertise can make a real impact during an exciting period of transformation and innovation.

About Us

Genomic Diagnostics provides comprehensive genomic testing, spanning oncology, reproductive health, inherited disease and pharmacogenomics, to an extensive network of public and private hospitals and community referrers across Australia. Our primary focus is to provide high-quality and timely genomic information to assist in diagnosis and clinical decision-making.

Genomic Diagnostics is part of Healius, one of Australia’s leading healthcare companies, providing the scale and backing of a national diagnostics network. Healius operate more than 80 medical laboratories and approximately 2,000 patient collection centres across metropolitan, regional and remote communities throughout Australia.

About the Role

As the Inherited Disease Team Leader, you will be a trusted senior member of the Genomic Diagnostics team based at our Heidelberg laboratory,



providing high-level clinical and scientific expertise across the inherited genomics portfolio. You’ll work closely with pathologists, clinicians and laboratory colleagues to deliver high-quality inherited disease testing and drive improvements in testing quality, turnaround times and scientific rigour.

Key responsibilities:

Oversee and guide a team of scientists, technicians and pathology assistants in the inherited disease stream

Oversee and manage the whole exome (or genome) sequencing workflow, including library preparation, sequencing, data analysis, curation and reporting.

Perform variant analysis and clinical interpretation, and prepare, review and authorise high-quality inherited disease genomic reports.

Liaise with internal stakeholders (Chief Scientist, Genetic Pathologist, Clinical Geneticist and Genetic Counsellor) on triage, variant analysis and reporting of whole exome and genome sequencing data.

Ensure all testing and reporting meet NPAAC/NATA ISO 15189 requirements and internal quality standards.

Maintain high standards of laboratory practice, including documentation, QC, QAP participation and equipment oversight.

Provide subject matter expertise to scientists,



trainees and clinical colleagues on variant curation and complex case interpretation.

Drive workflow optimisation, automation and continuous improvement to support increasing testing volumes, turnaround times and service development.

Escalate complex, abnormal or urgent results appropriately to senior scientific and clinical stakeholders.

About You

You are an experienced senior or clinical scientist with deep expertise in genomic diagnostics and strong scientific judgement. You're confident interpreting complex NGS data, experienced in managing high-complexity testing and comfortable operating at a leadership level within a clinical laboratory workplace. You're motivated by the opportunity to apply your specialist knowledge to challenging inherited genomics cases and shape the development of a growing service.

To be successful, you will need to meet the mandatory requirements:

A relevant tertiary qualification in Science/Medical Science, with a Masters in diagnostic genomics or equivalent.

Highly regarded: PhD, FHGSA (Molecular Genetics) or Fellowship of RCPA – Faculty of Science, or equivalent professional fellowship.

Significant clinical or diagnostic laboratory experience (ideally 8+ years) within genomics, molecular pathology or related disciplines.

Strong experience with whole exome and/or whole genome sequencing, including variant curation, interpretation and clinical reporting.

Experience in analysis and reporting of carrier screening, hereditary cancer, somatic oncology, and/or haematological neoplasms.

Experience with laboratory automation and emerging genomic technologies

Demon

📌 Team Leader (Melbourne)
🏢 Healius
📍 Melbourne