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To perform and provide analyses for low to high complex diagnostic testing in the relevant section.
To adhere to and assist in enforcing policies and procedures to assure results of the highest level of quality to physicians and their patients.
Actively participates in the technical and analytical work of the section.
Liaises with Supervisor on appropriateness of tests, results and additional testing as required.
Monitors, records, and reports back results, participating in discussion to rectify areas of concern if necessary.
Receives specimens submitted to laboratory and utilizes policies and procedures for requisition and specimen requirements to determine whether the submitted specimen can be processes for analysis.
Assures proper storage and procedures for specimens that cannot be immediately analysed.
Conducts preliminary specimen preparations for the analytical process through centrifugation of blood specimens, aliquoting of blood and body fluids and distribution of the prepared specimens to the appropriate sections of the laboratory.
Answers inquiries regarding specimen handling, results, and other technical information. Appropriately, assists clinicians with requests and seeks out resources necessary when information is not available to answer questions.
Ensures policies and procedures for the sections are adhered to.
Participates in the external quality assurance schemes that the department subscribes to.
Assists in establishing and maintaining continual compliance with Quality Standards, policies, and procedures to ensure achievement of and maintaining CAP, JCI, AABB and ISO15189 standards in the section.
Practices the proficient and safe use of all equipment necessary for the completion of all duties and responsibilities by following all maintenance, safety and quality controls policies, and procedures.
Takes responsibility for the maintenance and safe use of equipment within the section.
Participates in the implementation of new methodologies under the direction of the Supervisor.
Provides specialized support in the implementation of new clinical laboratory procedures, equipment, and processes. Furnishes continued technical support after clinical implementation.
• Functional knowledge and clinical experience in Clinical laboratories.Knowledge of and experience with Clinical laboratory safety and risks.Knowledge of ISO 15189/CAP/JCI/AABB standards and guidelines.Strong analytical and decision-making skills.Excellent communication and interpersonal skills.Proficiency with Microsoft Office suite
• ERP knowledge preferably SAP functional skills are a requirement to be successful in this role.
Minimum 8 years of experience in clinical laboratories as a licensed clinical scientist or technologist (required)
Minimum 3 years as a Technologist in a CAP or ISO15189 laboratory (required)
Minimum 2 years in GCC (preferred)
You'll no longer be considered for this role and your application will be removed from the employer's inbox.