Clinical Laboratory Associate II (1st Shift, Thursday-Sunday, 4x10 Hour Days, 5:00am - 3:30pm)

The Clinical Laboratory Associate II (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 backup 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.

Onboarding Training: For the first six weeks of employment onsite training will take place during the first shift Monday through Thursday.

Essential Duties and Responsibilities:

In accordance with California Business and Professions Code BPC 1269 the following activities may be performed under the supervision of the laboratory director or appropriately licensed personnel:

• 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 laboratorys 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;
• In the case of qualitative and semiquantitative tests the unlicensed personnel may add the test reagent to the specimen or vice versa but the results must be read by the laboratory director or appropriately licensed personnel. 
• 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 laboratorys established performance specifications; 
• Assist with internal audits and inspection preparation
• Organize the 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; and
• 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;
• Bachelors 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; and
• Ability to participate in projects update others on progress and complete assignments as expected.

Additional Information :

For positions based in Palo Alto CA or Redwood City CA the hourly range for this fulltime position is $36.29 to $49.92. The range does not include benefits and if applicable overtime bonus commission or equity.

Within the range individual pay is determined by work location and additional factors including but not limited to jobrelated skills experience and relevant education or training. If you are selected to move forward the recruiting team will provide details specific to the factors above.

Employee may be required to lift routine office supplies and use office equipment. Majority of the work is performed in a desk/office environment; however there may be exposure to high noise levels fumes and biohazard material in the laboratory environment. Ability to sit for extended periods of time.

Guardant Health is committed to providing reasonable accommodations in our hiring processes for candidates with disabilities longterm conditions mental health conditions or sincerely held religious beliefs. If you need support please reach out to 

Guardant Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin or protected veteran status and will not be discriminated against on the basis of disability.

All your information will be kept confidential according to EEO guidelines.

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