Clinical Laboratory Associate II (WED- SAT MN Shift 9pm-7:30am PT)
Guardant Health
Summary
The Clinical Laboratory Associate (CLA) II is responsible for supporting the daily operations of the Clinical Laboratory and assisting the Clinical Laboratory Scientist (CLS) during patient testing. In addition to the primary role of CLA, there will be a need to provide back-up support to the other groups (Reporting, Biospecimen Management, QC, etc.). The CLA II may serve as a lead to the CLA team to coordinate tasks, divide workload, manage equipment usage schedule and documents reviewing/filing process as assigned. The CLA II has demonstrated the skills and competency to assist the CLSs in automated sample processing and in all other support functions. The nature of the work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and schedules, and the ability to work independently in a team environment.
Job description
Shift Details
Wednesday-Saturday; MN 9pm-7:30am PT
Essential Duties and Responsibilities
- Sample collection or receipt, sample preparation, labeling, handling, preservation or fixation, assay processing or preparation, and/or transportation and storage of specimens
- Assist the CLSs in a licensed clinical laboratory in performing sample processing
- Assist the CLSs during automated methods of patient testing
- Perform routine equipment maintenance according to the laboratory’s standard operating procedures
- Create sample batches, print labels and label tubes and plates
- Assist licensed testing personnel in troubleshooting activities
- Prepare and store reagents for sample processing and sample archiving
- Order and stock laboratory supplies
- Print and file of laboratory records
- Check, monitor and resolve routine cold storage temperature and laboratory temperature and initiate a service request as necessary
- Perform general laboratory tasks include cleaning of racks, laboratory equipment and benches
- Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications
- Assist with internal audits and inspection preparation
- Organize and maintain schedule of the laboratory and equipment
- Ensure calibration of laboratory equipment is scheduled and performed on time
- Ensure laboratory equipment is properly labeled
- Write and revise standard operating procedures under supervisor instruction, as needed
- Identify process improvement opportunities and report to laboratory management
- Perform other duties as assigned
- Report all concerns of test quality and/or safety to the Laboratory Supervisor, Laboratory Director or Safety Officer
Qualifications
- Minimum of Associate degree or equivalent required
- Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field preferred
- At least one year of Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred
- Strong computing skills
- Proficiently executed good documentation practices
- Advanced knowledge of reagent stability and storage, quality control policies, and factors that influence test results
- Demonstrates strong practical reasoning and sound judgment
- Skilled in making informed and effective decisions
- Exhibits exceptional attention to detail and a strong commitment to precision in all tasks
- Strong communicator with ability to maintain open communication with internal employees, managers
- Proficient in giving and receiving constructive feedback, fostering open communication and continuous improvement
- Capable of independently executing tasks with minimal direction, while maintaining a collaborative approach that avoids complete isolation
- Ability to divide workload evenly among CLAs in accordance with operational needs
- Ability to prioritize tasks with a high emphasis on quality and time
- Proactively initiate and drive projects, consistently contributing innovative solutions and seizing opportunities for process improvement
- Ability to participate in projects, update others on progress and complete assignments as expected
AI & Digital Fluency
Demonstrate curiosity, sound judgment, and the ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements to improve the efficiency, effectiveness, and quality of work.
Requirements
- Minimum of Associate degree or equivalent required
- Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field preferred
- At least one year of Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred
- Strong computing skills
- Proficiently executed good documentation practices
- Advanced knowledge of reagent stability and storage, quality control policies, and factors that influence test results
- Demonstrates strong practical reasoning and sound judgment
- Skilled in making informed and effective decisions
- Exhibits exceptional attention to detail and a strong commitment to precision in all tasks
- Strong communicator with ability to maintain open communication with internal employees, managers
- Proficient in giving and receiving constructive feedback, fostering open communication and continuous improvement
- Capable of independently executing tasks with minimal direction, while maintaining a collaborative approach that avoids complete isolation
- Ability to divide workload evenly among CLAs in accordance with operational needs
- Ability to prioritize tasks with a high emphasis on quality and time
- Proactively initiate and drive projects, consistently contributing innovative solutions and seizing opportunities for process improvement
- Ability to participate in projects, update others on progress and complete assignments as expected
Company overview
Guardant Health, Inc. is a leading precision oncology company headquartered in Palo Alto, California, focused on transforming cancer care through advanced blood and tissue testing technologies. Founded in 2012 by Helmy Eltoukhy and AmirAli Talasaz, who serve as co-CEOs, the company specializes in liquid biopsy tests that detect cancer from circulating tumor DNA in blood samples. Guardant Health's flagship product, Guardant360, was the first comprehensive liquid biopsy test approved by the FDA for tumor mutation profiling and companion diagnostics in non-small cell lung cancer. The company has expanded its portfolio to include Guardant Reveal for residual disease monitoring, Guardant360 TissueNext tissue testing, and Shield, the first FDA-approved blood test for colorectal cancer screening. Guardant Health operates globally with approximately 1,999 employees and generates revenue from precision oncology testing services for clinical and biopharmaceutical customers, as well as development services and technology licensing. The company's innovative approach enables earlier cancer detection, treatment selection, and monitoring, helping to improve patient outcomes across all stages of cancer care.