Technologist II – Special Chemistry

    68
    • Full Time
    • Qatar

    Sidra Medicine

    KEY ROLE ACCOUNTABILITIES:
    Organizes and participates in the work of the section. Works unsupervised, but under the direction of the Supervisor – Clinical Biochemistry.
    Actively supervises other BMS staff within their section to ensure an efficient throughput of work.
    Assists the Supervisor – Clinical Biochemistry and the Clinical Director – Pathology in the implementation of management decisions affecting the sections, as documented above.
    Maintains co-operation between the section and between disciplines by regular liaison with other section leads and senior staff. This includes attendance at staff meetings.
    Leads by good example in order to motivate staff to create high quality work, interest and contribution.
    Actively participates in the technical work of the section.
    In liaison with the Supervisor – Clinical Biochemistry ensures adequate stocks of reagents and consumables are available for the efficient running of the service.
    Uses LIS to generate workload statistics and run queries.
    Answers enquiries and communicates patient results to clinicians, surgeons and nursing staff both internally and external to Sidra.
    Provides specialist technical advice on specimen handling to clinicians, surgeons and nursing staff.

    In liaison with Supervisor – Clinical Biochemistry and Clinical Director – Pathology provides technical advice on, and assists in the selection of new equipment.
    Monitors and advises on the use of reagents and consumables in the section.
    Takes responsibility for the maintenance and safe use of equipment within the section.
    Helps to ensure the provision of a high quality, cost-effective service with the emphasis on quality assurance in all aspects of the section supervised by monitoring and audit of internal quality control.
    Participates in the external quality assurance schemes that the department subscribes to. Monitors, records and reports back results, participating in discussion to rectify areas of concern if necessary.
    Carries out corrective action when the quality control procedures fail.
    Assists in ensuring and maintaining CPA-ISO15189 standards in the section.
    Ensures policies and procedures for the sections are adhered to.
    Participates in the training, theoretical and practical, of technical staff in the section for which they are responsible in methodologies, principles and procedures by way of tutorials, presentations and seminars.
    Updates, reviews and implements new methodologies in the section under the direction of the Supervisor – Clinical Biochemistry and Clinical Director – Pathology.
    Participates in research and development as directed by the Supervisor – Clinical Biochemistry and Clinical Director – Pathology.
    Adheres to Sidra’s standards as they appear in the Code of Conduct and Conflict of Interest policies
    Adheres to and promotes Sidra’s Values

    To apply for this job please visit fa-epxn-saasfaprod1.fa.ocs.oraclecloud.com.

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