Technologist I - Pathology Sciences

Working with the Laboratory supervisor and the Technologist II, the Technologist I - Pathology Sciences assists in the validation of all equipment and processes within the laboratory, preparation of policies and procedures in accordance with CAP-ISO15189 and JCI, and training of staff as appropriate to the expertise and experience of the post-holder. In a fully operational laboratory. The Technologist I - Pathology Sciences performs a broad range of technical and analytical work with a high level of individual skill and judgment, under minimal supervision. The incumbent is required to observe and maintain a high standard of laboratory health, safety and risk procedures; and works to departmental Standard Operating Procedures, and current professional standards. S/he is actively involved in the laboratory’s continuing professional development program, preparing and delivering presentations to a range of staff, attending internal and external lectures, and undertaking additional training courses as required. The Technologist I - Pathology Sciences is part of a team of Biomedical Scientists/ Technologists delivering high quality services in their specialty.  The Technologist I - Pathology Sciences will be required to work and rotate on 24 hours shifts and weekends.

KEY ROLE ACCOUNTABILITIES:

• Performs a wide range of standard and complex technical roles within the section, involving a variety of molecular tests on different platforms.
• Interprets results obtained from above and prepares test reports for checking and verification by senior staff.
• Liaises with Technologist II and Laboratory Supervisor on the appropriateness of tests, results and additional testing as required.
• Monitors, records and reports back results, participating in the discussion to rectify areas of concern if necessary.
• Maintains the cleanliness of the laboratory including work surfaces, biosafety hoods and equipment according to the standard operating procedures.
• Maintains storage of clinical specimens, nucleic acid extracts and reference and control materials.
• Maintains co-operation between the sections and between disciplines by regular communication with other Technologists and senior staff.
• Responsible for ensuring adequate stocks of reagents and consumables are available for the efficient running of the service.
• In liaison with the Technologist II and the Laboratory Supervisor, provides technical advice on, and assists in the selection / validation of new equipment.
• Takes responsibility for the maintenance and safe use of equipment within the section.
• Helps to ensure the provision of 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.
• Actively involved in the external quality assurance schemes that the department subscribes to.
• Uses Laboratory Information System for specimen login, record assay-specific parameters and stock records, generates test reports, generates workload statistics and run queries.  Assesses the quality of data according to defined criteria.
• Carries out corrective action as advised when the quality control procedures fail.
• Assists in ensuring the achievement of and maintaining CAP and 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 methodologies, principles and procedures by way of tutorials, presentations and seminars.
• Participates in the implementation of new methodologies under the direction of the Technologist II and Laboratory Supervisor.
• Participates in research and development as directed by the Technologist II and the Laboratory Supervisor.
• 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

In view of the evolving needs and opportunities within Sidra, this position may be required to perform other duties as assigned and reporting relationships may vary.

• 2+ years of relevant experience in a diagnostic molecular laboratory
• Experience/ understanding of LIS operations
• Experience in validation of new equipment and services
• No minimum experience requirement for Qatar University / CNAQ Graduates only

• Professional License in the country of origin 
• Meets the requirement for licensure by the Qatari’s Supreme Council of Health which includes a Prometric exam

• Competent in a broad range of molecular techniques and methodologies 
• Knowledge/understanding of ISO15189/CPA/CAP/ JCI standards and guidelines
• Able to work as part of team, but also independently with minimal supervision
• Ability to work under pressure
• Excellent communications skills both written and oral
• Proficiency with Microsoft Office suite
• Fluency in written and spoken English