About this opportunity:
As a Clinical Laboratory Scientist II (CLS II) you will perform high-complexity laboratory testing on patient specimens, perform quality control and quality assurance procedures, and comply with all applicable local, state, and federal laboratory requirements. The work requires keeping meticulous and organized records; excellent attention to detail; and the ability to flexibly prioritize multiple tasks and schedules, analysis, and results. The CLS II will be involved with training, troubleshooting, leading projects, meeting project deliverables, and understanding and implementing laboratory goals. The CLS II must also demonstrate excellent communication skills, proactively communicating team goals and priorities clearly, openly and objectively, and communicating changes, issues and challenges in all directions of the organization.
This role reports to the Supervisor, Analytical Laboratory.
Working Hours:
The standard hours of this position are Monday - Friday 7:30am-4:00pm (subject to change to support business needs). Periodic extended hours and weekend rotations will be required for approximately 6 months.
What you’ll do:
- Perform high-complexity laboratory tests, procedures, and analyses according to the laboratory’s standard operating procedures (SOPs) and work instructions
- Collaborate with the Development Team and the Automation Team to execute assay improvement experiments, new assay configurations, and validations
- Operate, maintain, troubleshoot, and document routine preventive maintenance on laboratory equipment according to the laboratory’s SOPs for machines and devices including, but not limited to, the following: centrifuges, freezers, refrigerators, pipettors, NovaSeq units, Bravo units, Hamilton units, and work cells, as needed
- Review, interpret, and report patient results in the company’s laboratory information management system (LIMS) as assigned
- Independently identify and troubleshoot high-complexity assay problems that adversely affect the test performance
- Perform, review, and document laboratory quality control procedures
- Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications
- Report all quality issues and/or safety concerns to the laboratory supervisor or safety officer
- Train existing laboratory personnel in new procedures and train new laboratory personnel
- Prepare reagents required for testing
- Perform and document reagent qualification per the approved protocols
- Provide direct supervision of the work of unlicensed laboratory personnel during the analytical phase of testing
- Write and review procedures, documents, and forms
- Communicate effectively with cross-functional teams
- Perform other laboratory duties as assigned
Must haves:
- Valid California Clinical Laboratory Scientist license (Generalist preferred, CGMBS accepted)
- Bachelor of Arts or Science in Biomedical Laboratory Science, Clinical Science or related field
- Working knowledge of local, state, and federal laboratory regulations
- One to 2 years of Clinical Laboratory experience or equivalent
- Ability to integrate and apply feedback in a professional manner
- Ability to analyze and problem solve complex issues that may impact test performance
- Experience working with laboratory automation such as Hamilton or Bravo liquid handlers
- Flexibility to variable shift start times depending on operational needs
Nice to haves:
- Laboratory testing experience within the last five years preferred
- High volume laboratory experience preferred
- Experience in molecular biology techniques preferred
- Strong automation and computing skills
Benefits and additional information:
The US target range of our base hourly rate for new hires is $58.92 - $70.17. You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered. Please note that individual total compensation for this position will be determined at the Company’s sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education. We invite you to check out our career page @ freenome.com/job-openings/ for additional company information.
Freenome is proud to be an equal-opportunity employer, and we value diversity. Freenome does not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.
Applicants have rights under Federal Employment Laws.
- Family & Medical Leave Act (FMLA)
- Equal Employment Opportunity (EEO)
- Employee Polygraph Protection Act (EPPA)
California applicants please review the CCPA Notice at Collection here:
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