Clinical Laboratory Scientist I - Temp - 7:00am-3:30pm
Publication date:
17 September 2024Workload:
100%- Place of work:Redwood - 301 Penobscot
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Position Overview
The Clinical Laboratory Scientist I is responsible for performing high complexity laboratory testing on patient specimens, interpreting and reporting patient results, performing quality control and quality assurance procedures, and complying with all applicable local, state, and federal laboratory requirements.
This is a temporary full time position with a Monday - Friday 7:00am - 3:30pm schedule onsite at our Redwood City location.
Essential Duties
Include, but are not limited to, the following:
- Perform laboratory tests, procedures, and analyses according to the laboratory’s standard operating procedures.
- Perform, review, and document laboratory quality control procedures.
- Operate, maintain, and troubleshoot laboratory equipment.
- Prepare reagents required for laboratory testing.
- Review, interpret, and report patient results.
- Identify and troubleshoot basic problems that adversely affect test performance.
- Supervise unlicensed laboratory personnel.
- Assist with training new laboratory personnel on current and new procedures, as needed.
- Maintain sufficient inventory of laboratory supplies for daily operations.
- Participate in testing and validation of new laboratory equipment and procedures, as needed.
- Communicate effectively with coworkers and non-laboratory personnel.
- Maintain stringent standards for quality, identifying any issues which might adversely impact the quality of test results and/or employee safety, and communicating these to the appropriate management representatives as necessary for resolution.
- Perform quality assurance activities for internal audits and inspection preparation.
- Prioritize a positive work environment by investing time in building relationships and trust with all stakeholders.
- Ability to analyze and problem solve basic issues that impact test performance.
- Strong communicator with ability to maintain open communication with internal employees, managers, and customers, as needed.
- Ability to integrate and apply feedback in a professional manner.
- Ability to prioritize and drive to results with a high emphasis on quality.
- Ability to work as part of a team.
- Ability to multi-task and be flexible with tasks and schedules.
- Apply excellent attention to detail.
- Effective written and verbal communication skills
- Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
- Support and comply with the company’s Quality Management System policies and procedures.
- Maintain regular and reliable attendance.
- Ability to act with an inclusion mindset and model these behaviors for the organization.
- Ability to work designated schedule.
- Ability to work weekends, as needed.
- Ability to work overtime, as needed.
- Ability to list up to 25 pounds for approximately 5% of a typical working day.
- Ability to work seated for approximately 35% of a typical working day. Ability to work standing for approximately 65% of a typical working day.
- Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 40% of a typical working day.
- Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.
- Ability to comply with any applicable personal protective equipment requirements.
- Ability to use various types of laboratory equipment; including pipettes.
- May perform repetitious actions using lab tools.
- Ability to use near vision to view samples at close range.
- May be exposed to hazardous materials, tissue specimens, blood or blood products and instruments with moving parts, lasers, heating and freezing elements, and high-speed centrifugation.
Minimum Qualifications
- Bachelor’s Degree in Clinical Laboratory Science, Medical Technology, Chemical or Biological Sciences; or Military Education equivalent.
- Completion of a CLS, CGMBS, or equivalent training program at an accredited institution.
- Possession of a valid California CLS/CGMBS license or CGMBS Trainee license and maintain throughout employment in position.
- Professional working knowledge of local, state, and federal laboratory regulations.
- Strong computer skills to include internet navigation and email usage.
- Demonstrated ability to perform the Essential Duties of the position with or without accommodation.
- Authorization to work in the United States without sponsorship.
Preferred Qualifications
- Experience in high volume laboratory.
- Experience with laboratory automation.
- Experience working with laboratory information management system (LIMS).
- Training in molecular biology techniques.
- Proficient in Microsoft Office programs, such as Excel, Power Point, and Word.
If you require an accommodation, please contact us E-Mail schreiben.
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Applicable portions of the Company’s affirmative action program are available to any applicant or employee for inspection upon request.
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