Business Segment
Healthcare Eastern & African Growth Markets
About Us
What do you envision for your future? At GE Healthcare, we strive to see life more clearly. Our "healthymagination" vision for the future invites the world to join us on our journey as we continuously develop innovations focused on reducing healthcare costs, increasing access and improving quality and efficiency around the world.
We are a $17 billion unit of General Electric Company (NYSE: GE), employing more than 46,000 people worldwide and serving healthcare professionals in more than 100 countries. We believe in our strategy - and we'd like you to be a part of it. As a global leader, GE can bring together the best in science, technology, business and people to help solve one of the world's toughest challenges and shape a new age of healthcare.
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Role Summary/Purpose
The CLS I works under minimal supervision and is responsible for complex laboratory procedures and handles all types of specimen submitted into the department in processing task assigned.
Essential Responsibilities
- Perform simple to complex assays by following the established departmental protocols. - Read and understand all DOPs related to the department and adhere to all rules and protocols. - Read and record critical assay dependent measurements. - Perform analysis accurately on a daily basis for the discipline assigned to CLS per the department. - Reporting via the laboratory's LIS system. - Prepare clinical specimens for testing and identify specimen related problems. - Identify any problems that may adversely affect test performance or reporting of test results and either, correct the problems or immediately notify the general supervisor or director. - Take a main role in performing QC for reagents and chemicals and by using the DOPs. - Review and approve Quality control and Quality Assurance results. - Assist the supervisor in ensuring an efficient workflow operation and reports any delays and problems that can cause significant delay on the workflow process to supervisors, or technical director. - Monitor TAT and workflow. - Assist in preparation of validation documentation of new tests and procedures as required by the company. - Cleaning and maintenance of the lab equipment. - Maintain laboratory in a clean, functional state, as well as cleaning or performing scheduling equipment and instrument maintenance / calibration / certification, as required. - Adhere to department rules and protocols as well as company regulations stated in the Employee handbook. - Adheres to Department Specific Safety Guidelines. - Standing, sitting, walking, bending, reaching, manual manipulation, and lifting up to 15 pounds. - Other duties as assigned by Medical Laboratory Director or VP of Operations. The above listing represents the general duties considered essential functions of the job and is not to be considered a detailed description of all the work requirements that may be inherent in the position. Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2. Complete all planned Quality & Compliance training within the defined deadlines 3. Identify and report any quality or compliance concerns and take immediate corrective action as required 4. Be able to follow depart
Job Details
| Date Posted: | 2013-09-13 |
| Job Location: | Riyadh, Saudi Arabia |
| Job Role: | Other |
| Company Industry: | Other |
Preferred Candidate
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