Clinical Laboratory Scientist I/II (Cancer Dx) - Irvine CA - TalentZok
Irvine, CA
About the Job
Clinical Laboratory Scientist I/II (Cancer Dx) - Irvine CA
OVERVIEW
Are you looking for a new opportunity to join an exciting multinational healthcare company that provides actionable genomic information to personalize the diagnosis and treatment of cancer as a key member of their coveted CLS team? Our client is a market leader in the important and growing field of molecular diagnostics, is growing again fast, and is offering $37/hr - $51/hr DOE, excellent fully employer-paid healthcare benefits, and progressive career opportunity!
Open shifts:
- Sun – Thurs, 4:00 am – 12:30 pm
- Tues – Sat, 4:00 pm – 12:30 am
- Tues – Sat, 4:00 pm – 12:30 am
- Sun – Thurs, 4:00 pm – 12:30 pm
- Tues – Sat, 12:00 am – 8:30 am
Immediate opening for a Clinical Laboratory Scientist I/II in Orange County, CA who possesses:
- Degree in Science with current CA CLS license (Generalist or CGMBS)
- *preferred* Genetic Molecular Biology experience (Real Time PCR)
- *preferred* LIMS, LIS system experience
- *preferred* basic knowledge of Hamilton Robotics
Please send your resume to mturner@simplybiotech.com and call (858) 356-6772
KEY RESPONSIBILITIES INCLUDE:
- Perform all manual technical procedures relating to specimen preparation, specimen type, protocols and procedures.
- Operate automated laboratory instrumentation as assigned including troubleshooting, maintenance and repair procedures as required.
- Consistently and accurately transcribe patient test results from raw data generated from an instrument into the Laboratory Information Management System (LIMS).
- Responsible for the accurate documentation of all testing activities including but not limited to patient specimens, proficiency testing, quality control results, performance of preventive maintenance/calibration of instruments, and LIS results entry.
- Responsible for the documentation of corrective actions when test systems deviate from the laboratory's established performance specifications.
- Responsible for the inspections, labeling, and storing of incoming materials from the QC Department.
- Maintain complete and document records in real-time includes but is not limited to, department logs, files, and worksheets.
- Responsible for administering and performing competency assessment testing (biennially for new employees employed less than one year) when scheduled.
- Responsible for meeting or exceeding results for key performance indicators and quality metrics.
- Responsible for completing assigned tasks in MasterControl within the required timeframes.
For immediate consideration, please send your resume to mturner@simplybiotech.com and call (858) 356-6772
Source : TalentZok