Invivoscribe
Invivoscribe provided pay range
This range is provided by Invivoscribe. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $50.00/hr - $55.00/hr
Invivoscribe is an industry pioneer, dedicated to Improving Lives with Precision Diagnostics®. Invivoscribe has been the global leader in driving international standardization of testing and accelerating patient access to the newest and best cancer treatments for over 30 years. Headquartered in sunny San Diego, California with locations across the world, we offer a comprehensive portfolio of products and services. We work with key collaborators to develop molecular assays, reagents, controls and bioinformatics tools under ISO 13485 design control that are used by over 700 clinical laboratories in over 160 countries. Our global network of laboratories offers internationally standardized next generation molecular and flow cytometry panels to support drug development and accelerate drug approvals worldwide. We work with pharmaceutical partners and international regulatory agencies across the globe to develop companion diagnostics, which are necessary to gain approval of new drugs and treatments for cancer patients. For 30 years, we have been at forefront of precision diagnostics, and we’re just getting started!
Clinical Laboratory Scientist II This position provides professional customer service to our clients. CLS works in a team environment to ensure timely and quality test results. The CLS II works with guidance as needed to changes in the workflow.
Core Responsibilities
Performs all assigned duties in compliance with internal SOPs and external regulations. Brings compliance issues to the attention of management.
Ensures all aspects of pre-analytic workflow including order entry, specimen collection, and processing. Evaluates specimens for appropriateness and documents unacceptable specimens.
Operates laboratory equipment such as Thermocyclers, Next Generation testing platforms, cell counters, UV-Vis Spectrophotometer, fluorometer, electrophoresis testing platforms, etc. Uses automated equipment that analyzes multiple samples at the same time.
Performs NGS Library Preparation, complex gene panel NGS tests, and quantitative and normalization of isolated DNA.
Verifies reagents and supplies, meets defined acceptability criteria upon receipt and prior to use and acts to ensure unacceptable items are removed from use.
Assists with inventory counting and prioritizes testing based on assignment or established priorities; completes testing within defined turn‑around times.
Performs technical review, data analysis and interpretation. Reviews results for completeness, correctness and consistency within defined test system.
Performs moderate to advanced troubleshooting and repair and escalates issues when necessary.
Ensures accurate results are reported within established time frames; retains specimens appropriately and makes test results and/or current status available upon inquiry.
Assists with required Quality Management System responsibilities including initiating Quality Occurrence Reports.
Follows all required safety procedures; assumes a proactive role in laboratory safety. Follows all required privacy, safety, and biohazard procedures and standards.
May assist with training of new employees.
Responsible for monitoring and troubleshooting temperature excursions on cold storage units.
Follows all proficiency testing (PT) policies and guidance.
Performs Phase-ins (prequalification of reagents or reagent QC).
Ensures HIPAA laws are followed and maintains patient and employee confidentiality.
Ensures supply and reagent levels are appropriate and notifies appropriate personnel when new supplies are needed.
Ensures integrity of Laboratory Information Management System (LIMS) by following established protocols and participating in its maintenance and enhancements.
You Bring
BS in Clinical Laboratory Science or scientifically related field with, typically, 2+ years of industry experience in a Clinical Laboratory. Equivalent combination of education and experience will be considered.
Licensed in California as a Clinical Laboratory Scientist.
Proficient computer and Microsoft Office program skills (Word, Outlook, Excel), and the ability to learn new software programs.
We Bring
A beautiful modern facility centrally located in San Diego County, with many jobs conducive to a hybrid work from home arrangement.
A safe, fully‑vaccinated, work environment.
A diverse and inclusive work environment where you will learn, grow, and make new friends.
#J-18808-Ljbffr
Base pay range $50.00/hr - $55.00/hr
Invivoscribe is an industry pioneer, dedicated to Improving Lives with Precision Diagnostics®. Invivoscribe has been the global leader in driving international standardization of testing and accelerating patient access to the newest and best cancer treatments for over 30 years. Headquartered in sunny San Diego, California with locations across the world, we offer a comprehensive portfolio of products and services. We work with key collaborators to develop molecular assays, reagents, controls and bioinformatics tools under ISO 13485 design control that are used by over 700 clinical laboratories in over 160 countries. Our global network of laboratories offers internationally standardized next generation molecular and flow cytometry panels to support drug development and accelerate drug approvals worldwide. We work with pharmaceutical partners and international regulatory agencies across the globe to develop companion diagnostics, which are necessary to gain approval of new drugs and treatments for cancer patients. For 30 years, we have been at forefront of precision diagnostics, and we’re just getting started!
Clinical Laboratory Scientist II This position provides professional customer service to our clients. CLS works in a team environment to ensure timely and quality test results. The CLS II works with guidance as needed to changes in the workflow.
Core Responsibilities
Performs all assigned duties in compliance with internal SOPs and external regulations. Brings compliance issues to the attention of management.
Ensures all aspects of pre-analytic workflow including order entry, specimen collection, and processing. Evaluates specimens for appropriateness and documents unacceptable specimens.
Operates laboratory equipment such as Thermocyclers, Next Generation testing platforms, cell counters, UV-Vis Spectrophotometer, fluorometer, electrophoresis testing platforms, etc. Uses automated equipment that analyzes multiple samples at the same time.
Performs NGS Library Preparation, complex gene panel NGS tests, and quantitative and normalization of isolated DNA.
Verifies reagents and supplies, meets defined acceptability criteria upon receipt and prior to use and acts to ensure unacceptable items are removed from use.
Assists with inventory counting and prioritizes testing based on assignment or established priorities; completes testing within defined turn‑around times.
Performs technical review, data analysis and interpretation. Reviews results for completeness, correctness and consistency within defined test system.
Performs moderate to advanced troubleshooting and repair and escalates issues when necessary.
Ensures accurate results are reported within established time frames; retains specimens appropriately and makes test results and/or current status available upon inquiry.
Assists with required Quality Management System responsibilities including initiating Quality Occurrence Reports.
Follows all required safety procedures; assumes a proactive role in laboratory safety. Follows all required privacy, safety, and biohazard procedures and standards.
May assist with training of new employees.
Responsible for monitoring and troubleshooting temperature excursions on cold storage units.
Follows all proficiency testing (PT) policies and guidance.
Performs Phase-ins (prequalification of reagents or reagent QC).
Ensures HIPAA laws are followed and maintains patient and employee confidentiality.
Ensures supply and reagent levels are appropriate and notifies appropriate personnel when new supplies are needed.
Ensures integrity of Laboratory Information Management System (LIMS) by following established protocols and participating in its maintenance and enhancements.
You Bring
BS in Clinical Laboratory Science or scientifically related field with, typically, 2+ years of industry experience in a Clinical Laboratory. Equivalent combination of education and experience will be considered.
Licensed in California as a Clinical Laboratory Scientist.
Proficient computer and Microsoft Office program skills (Word, Outlook, Excel), and the ability to learn new software programs.
We Bring
A beautiful modern facility centrally located in San Diego County, with many jobs conducive to a hybrid work from home arrangement.
A safe, fully‑vaccinated, work environment.
A diverse and inclusive work environment where you will learn, grow, and make new friends.
#J-18808-Ljbffr