Interpret request forms and sort specimens according to tests (Respiratory viruses, Bordatella pertussis and Herpes).Swivel swabs for DNA and RNA extraction (purify) on MagnaPure 96.Run and analyse RT-PCR results on LightCycler® 480 and AusDiagnostics High-Plex 24 and Ultra-Plex 48 Systems.Validate results.Process urine and ThinPrep samples into cobas p480 instrument and cobas® 6800 system.Set up and housekeeping of instruments/equipment.Prioritize Urgent specimens.Help and guide staff members at all times specially during peak hour.Able to work under pressure and execute flawless work.Familiar with Ultra LIS and RICS.

Perform procedures to prepare different types of specimens (urine, faeces, swabs and fluids) for identification of microorganisms in the Microbiology Department. Duties also include sample reception; enter sample identification on to the computer system (Triple G). Prepare specimen for microscopy and culture.Faeces preparation for OCP (ova, cyst and parasite) tests, including viral strip test and Occult Blood in faeces when requested.

Lecture and pratical classes of Human Anatomy for Nursing, Pharmacy and Physiotherapy courses.Classes using data show and practical classes using plastic anatomic models.

Execute technical work in the laboratory related with the area which includes perform and guide collections. analysis and record data. Handle materials and substances through specific methods. Assist in the activities of teaching, research and post graduate studies. Specific duties were to organize chemical reagents following safety rules and stock list. Prepare solutions for all chemistry and biochemistry classes. Responsible for maintenance and housekeeping of the laboratory.

Receive, label and register samples of urine, plasma and leukocytes.Screen for inborn errors of metabolism in sample of urine and plasma.Newborn screening tests for Congenital Hypothyroidism and amino acidopathies like Phenylketonuria (PKU), Tirosinemias and Maple Syrup Urine Disease (MSUD).Quantification of phenylalanine and tyrosine in plasma sample for control of Phenilketonuria patients.Measurement of enzymatic activity of galactose-1-phosphate-uridil-transferase in blood sample to diagnose Classic Galactosemia or GALT deficiency.Measurement of enzymatic activity of hexosaminidase A and B in plasma and leukocyte sample for screening and diagnosis of Tay Sachs disease and Sandhoff disease.Quantification of glycosaminoglycans in urine for screening and control for patients with different type of Mucopolysaccharidosis disease.Measurement of enzymatic activity of Palmitoyl Thiosterase and Tripeptidil Peptidase for screening of Neuronal Ceroid Lipofuscinoses.Detection of 1kb deletion in CLN3 gene.Measurement od enzymatic activity of α-galactosidase A in plasma, leykocyte and blood spot in filter paper samples for screening and diagnosis for Fabry disease.