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.
Job Responsibilities 2
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.
Additional Responsibilities 3
Job Knowledge & Skills
• 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.
Job Experience
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)
Competencies
Accountability
Collaboration
Leadership
Quality
Resilience
Education
Bachelor's Degree in Biomedical Engineering or any related field
Power International Holding (PIH) is a diversified business conglomerate, grouped into 5 main sectors: General Contracting, Agro-Food Industries, Real Estate Development, Lifestyle (Hospitality, Entertainment & Catering) and General Services. To ensure the sustainability and success of each businesses within the various sectors, we are committed to providing every entity with the tools and resources together with the central functional support to enable development and growth. We work in specialization, to ensure that each business strives to achieve the organization’s objectives and goals. Grouping is done through focus and trade excellence of organization leaders who proactively work together in multi-disciplinary groups, ensuring that each business thrives and flourishes.
اطلب مساعدة الخبراء لكتابة سيرة ذاتية مميزة.
