To analyze, interpret and produce patient results on blood, urine, and CSF (cerebral spinal fluid) specimens and oral and nasal biopsies
To process, ship, and store specimens per protocol
Location:
PHRU - Tshepong Hospital, Matlosana, Klerksdorp
Key performance areas:
Processing PBMCs from whole-blood
Centrifuging or sample preparation with appropriate reagents
Storage of samples according to study protocols
Decontamination of all work surfaces/benchtops
Shipment of samples at appropriate conditions to different sites
Communicate routinely with the study coordinator and principal investigator
Receive labeled and captured samples from the Data Capturer
Check and verify that details on tubes and labels correspond
Check the suitability of samples to be analyzed xe2x80x93 no clots, not haemolysed, biopsies of sufficient size for downstream processing of biopsy explants as per the SOPs
Check the tests required and log them on the worksheet
Perform instrument and manual tests
Read slides under a microscope and comment (on morphology)
Analyse and interpret the results
Re-run tests as and when required
Follow up on incomplete tests and ensure completion thereof
Capture manual test results on laboratory information system (DISA)
Print the test results and correlate data with the DISA system
Initial print out and file it according to SOP
Contact relevant Clinicians (by telephone) if abnormal and CSF results have been produced
Record that feedback was given to relevant Clinicians/clients
Store specimens in fridge/freezer as per laboratory procedures (i.e. 7 days)
Centrifuging or preparing specimens with various reagents when necessary
Record the temperature of rooms and fridges with corrective action as applicable
Maintenance of all equipment used e.g. ensuring calibrations are up to date
Working according to the study protocol
Communicate routinely with the study coordinator, Principal Investigator, and study team
Perform internal and external quality control
Perform maintenance on instruments by inspecting equipment according to schedule
Check the expiry dates of reagents
Troubleshoot errors and contact Instrument Technicians or suppliers of equipment to repair if necessary
Resolve any quality-related problems and/or report it to management
Monitor the quality of specimens received
Provide training to site staff if specimen quality is poor
Monitor and control stock levels and advise if goods have to be ordered
Monitor and control workflows and turnaround times
Perform relevant administration i.e. filing, copying, faxing, etc.
Report any quality control issues to laboratory management
Print outstanding lists at the end of the shift to ensure that all tests have been performed and resulted xe2x80x93 hand over
Demonstrate cost consciousness and assist in meeting budgetary targets
Take ownership and accountability for tasks and demonstrate effective self-management
Follow through to ensure that quality and productivity standards of own work are consistently and accurately maintained
Maintain a positive attitude and respond openly to feedback
Take ownership of driving own career development by participating in ongoing training and development activities
Required minimum education and training:
A National Diploma in Biomedical Technology or a BSc in Medical Sciences will be advantageous
Required minimum work experience:
At least 2 years experience of working in a medical/clinical laboratory
Research experience advantageous
Professional body registration:
Registered with the Health Professions Council of South Africa as a Medical Technician, Independent practice
Desirable additional education, work experience, and personal abilities:
IATA trained
Good Clinical Practice (GCP) Certification
Certification in Good Clinical Laboratory Practice (GCLP) and basic health and safety
Exceptional organizational and administration skills with working knowledge of Microsoft Office and laboratory systems (DISA, Meditech)
Exposure to hazardous and infectious samples
Work in a pressurized environment in meeting turnaround times in high volumes
Communicate effectively with all laboratory staff. Liaise and maintain effective working relationships with external laboratories, Nurses, Clinicians, Couriers, Medical Representatives, equipment suppliers and Technicians
TO APPLY:
Only if you do meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CV.
Please Apply Online.
Please take note that the applicants who do not adhere to the above criteria will not be considered for the respective position.
The closing date for all applications: 19 December 2023.
Note AJ Personnel is fully POPI compliant.
Note WHC, in accordance with their Employment Equity goals and plan, will give preference to suitable applicants from designated groups as defined in the Employment Equity Act 55 of 1998 and subsequent amendments thereto.
Please note:
AJ PERSONNEL is only responsible for the advertising of the advertisement on behalf of their client Wits Health Consortium.
Wits Health Consortium will only respond to shortlisted candidates.
Candidates who have not been contacted within two weeks of the closing date can consider their applications to be unsuccessful.
AJ Personnel does not have any salary or other information regarding the position.