Part-Time Molecular Genetics Medical Scientist (0.63 FTE)

The Royal Melbourne Hospital; Melbourne; Vor Ort; AUD 42.000 - 60.000; Teilzeit

Benefits dieser Stelle

Salary packaging up to $12,000 tax‑fee

Generous leave entitlements

Monthly accrued day off (full-time/EBA

Work in Parkville Precinct

Zusammenfassung

The Royal Melbourne Hospital is seeking a part-time Medical Scientist (Grade 1/2) to contribute to the Molecular Genetics Laboratory within the Parkville Precinct. This role offers the opportunity to work in a leading molecular diagnostics environment as part of a large Victorian public pathology transformation.

You will handle specimens, support assay development, validation and genetic variant curation, while collaborating with a multidisciplinary team to deliver patient-centred pathology

Qualifikationen

• Bachelor of Science (Medical Laboratory Science, Molecular Biology, or equivalent).
• Excellent communication and teamwork skills.
• Commitment to delivering a patient focused service.
• Demonstrated effective & clear written and oral communication skills while working in a team.
• Ability to prioritise tasks to meet reporting deadlines.
• Experience in Molecular Haematology.
• Experience in using a Pathology LIS.
• Experience in using a Pathology Quality Management System (QMS).

Aufgaben

• Handling of biological specimens & referrals.
• Assay development and validation.
• Curation of genetic variants to determine their impact in human disease.

Kenntnisse

Molecular biology

Communication

Teamwork

Prioritisation

Ausbildung

Bachelor of Science (Medical Laboratory Science, Molecular Biology, or equivalent)

Tools

LIS

QMS

Jobbeschreibung

The Royal Melbourne Hospital is seeking a part-time Medical Scientist (Grade 1/2) to contribute to the Molecular Genetics Laboratory within the Parkville Precinct. This role offers the opportunity to work in a leading molecular diagnostics environment as part of a large Victorian public pathology transformation.

You will handle specimens, support assay development, validation and genetic variant curation, while collaborating with a multidisciplinary team to deliver patient-centred pathology