Clinical Laboratory Scientist I
7 days ago
Kelly is hiring a Clinical Laboratory Scientist I for one of our clients in Northridge, CA
- M-W 8 hour days
- Occasional Sundays (around 6 hours)
- Can be part time or full time
- Max pay $50/hr
- Contract position (2-3 months)
Must be CLS CA Licensed
SUMMARY
The Clinical Laboratory Scientist I is responsible for performing laboratory testing, recording and reviewing test results, preparing and labeling blood components.
Essential Responsibilities
- Perform all tasks in compliance with Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs) and other regulatory requirements.
- Properly use the Blood Product Information System, as well as authorize and perform system overrides as needed and within scope of authority and ensure to escalate system problems as/if encountered, to management.
- Accurately perform testing of blood products and donor samples (i.e., hematology counts (CBC), and pH).
- Accurately record, interpret, and report test results. Ability to recognize and appropriately handle unacceptable test results.
- Verify acceptability of blood samples.
- Prepare and pack blood samples for send-out testing.
- Properly use laboratory equipment.
- Properly perform, and complete comprehension of, quality control and preventative maintenance of laboratory equipment.
- Maintain laboratory records; adhere to proper flow of paperwork.
- Perform blood component preparation from whole blood and apheresis collections.
- Label blood products.
- Perform quarantine, destruction, and release of blood products.
- Prepare, perform and report proficiency testing. (i.e. CAP)
- Accurately report errors.
- Evaluate blood component QC testing.
- Review and/or order and maintain proper inventory levels of laboratory supplies/reagents.
- Prepare laboratory statistical reports.
- Identify and troubleshoot problems encountered in assigned tasks and properly document corrective actions. Confer with managerial staff for resolution of problems, if necessary.
- Inform supervisory staff of any recommendations for process improvement.
- Read and understand company and industry manuals and compliance standards, including SOPs, FDA requirements (cGMPs) and AABB regulations.
- Know and follow safety rules relative to area(s) of responsibility.
- Present a professional image to customers, internal and external.
- Revision of company SOP’s as required.
- Other duties as assigned.
Education, Experience, and Licensure
- Bachelor’s degree in biological, physical, or chemical sciences or medical technology is preferred
- At least 1 years of previous CLS working experience preferred
- Current state CLS Generalist license required.
- MT (ASCP), preferred.
- Blood donor center or transfusion service experience is a plus.
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