Done with errors on the page
Done with errors on the page
The successful candidate will accept accountability for each stage of the PCR process (quality processes, specimen identification, extraction, loading, setting up of runs on a variety of instrumentation, reporting) and use of the Laboratory Information System, for clinical output to comply with National Association of Testing Authorities / International Standardisation Organisation / Therapeutic Goods Administration / National Pathology Accreditation and Advisory Council (NATA/ISO/TGA/NPAAC) requirements.
Key competencies (role specific criteria)
You will be assessed on your ability to demonstrate the following:
Qualifications, registrations and other requirements