Senior Clinical Laboratory Scientist (2nd shift) at Illumina, Inc.
Posted in Science 11 days ago.
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Location: Redwood City, California
Do you want to make a difference? Illumina’s mission is to improve human health by unlocking the power of the genome. If that inspires you, let’s talk. We’ve built a culture fueled by innovation, collaboration and openness, and established ourselves as the global leader in DNA sequencing and array-based technologies. Our people and our technology change lives by driving advancements in life sciences, oncology, reproductive health, agriculture and other emerging markets. Life at Illumina is about working with teammates who are deeply passionate about what we do, because we know that our work has the power to improve lives. We’re an established company with a track record of phenomenal growth. Just check out our investor events and presentations to learn about our financial accomplishments. Our growth isn’t just in financials, we’ve been busy hiring the best and the brightest. Perhaps that’s why MIT has ranked Illumina near the top of its World’s Smartest Companies each of the last three years. If you thrive in a brilliant, fast-paced, and mission-driven environment, Illumina is the place for you. Join the journey of a lifetime. Join Illumina.
The Senior Clinical Laboratory Scientist is responsible for testing and reporting clinical laboratory results, as well as providing direct and constant supervision for the Clinical Laboratory Technicians (CLTs). Must have the ability to work 2nd shift and some weekends.
All About You:
- Performs and reports laboratory testing on clinical laboratory samples used to aide physicians in the diagnosis and treatment of patients.
- Selects, implements, and evaluates results for Quality Control materials used in statistical process control of laboratory assays.
- Troubleshoots assays and equipment for which QC materials fail to perform adequately.
- Participates in activities required to support all necessary licensure for the clinical laboratory, including quality management functions and on-site inspections of the laboratory.
- Responsible for maintaining updated understanding and knowledge of the methods employed in the laboratory and the use of the resulting information by physicians through continuing education activities.
- Trains other CLS personnel in laboratory methods and trains CLTs to assist CLSs in the laboratory methods. Required to provide direct and constant supervision of non-licensed personnel.
- May be required to assist in assay development activities. The testing personnel are responsible for specimen processing, test performance and for reporting test results.
Each individual performs only those high complexity tests that are authorized by the laboratory director and require a degree of skill commensurate with the individual's education, training or experience, and technical abilities.
Each individual performing high complexity testing must—
- Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results;
- Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens;
- Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed;
- Revise Work Instructions as required
- Follow the laboratory’s established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance;
- Be capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problems or immediately notify the Lead Clinical Lab Scientist General Supervisor, Technical Supervisor, Clinical Consultant, or Lab Director;
- Document all corrective actions taken when test systems deviate from the laboratory’s established performance specifications
- Current California CLS license
- Bachelor's degree
- 5+ years experience in a clinical laboratory setting; preferably with experience in a high complexity molecular testing environment. Is dependent upon Education and relevant Experience
- Ability to read, understand, and comply with detailed procedures that ensure the safety of all
- Must be flexible to work different shifts, such as weekends and evenings
- Demonstrated ability to work both independently, following detailed work instructions, and as part of a cohesive team that together completes daily sample intake and processing in a timely manner
- Ability to multi-task and prioritize duties to meet timelines
- Excellent communication, organizational and time management skills are essential
- Detail-oriented and conscientious
Illumina believes that everyone has the ability to make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. If you have a disability or special need that requires accommodation, please contact us at 858-255-5081. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf