Lead Clinical Laboratory Scientist Job at BillionToOne (Union City)

Lead Clinical Laboratory Scientist (CLS), Oncology

Join a team of brilliant, passionate innovators who wake up every day determined...

Location

United States , Menlo Park

Salary:

228788.00 USD / Year ▼

BillionToOne

Expiration Date

Until further notice

Requirements

Bachelor's degree in the chemical, physical or biological sciences
Minimum of 4 years of CLS experience in a clinical setting (molecular and/or high-complexity laboratory experience preferred)
A current California Clinical Laboratory Scientist License that meets requirements for Testing Personnel under CLIA regulations (42 CFR, part 493) (ASCP, CGMBS or generalist license is required)
Hands-on training and experience with manual molecular biology protocols, including DNA extraction, PCR, and automated liquid handlers
Advanced knowledge of Google Docs, Word, Excel, basic statistics and familiarity with LIMS systems and Next-Generation Sequencing
Strong attention to detail and ability to work flexibly and well under given timeframes.
Self-starter and dynamic team player with excellent verbal and written skills.

Job Responsibility

Lead clinical laboratory daily supervision in alignment with company values and mission
Hold General Supervisor delegation and responsibilities including oversight and support of day-to-day operations, scheduling, and troubleshooting
Manage CLIA direct reports including licensed and/or unlicensed staff (CLS, Clinical Laboratory Assistants)
Contribute to continuous process improvement projects including tech transfer, troubleshooting, training, and validations
Perform clinical laboratory assays to provide data for diagnosis, treatment, and prevention of disease
Perform quality control studies to ensure the accuracy of clinical data
Verify instrument performance by checking and calibrating specific lab instruments and documents data

What we offer

Working alongside brilliant, kind, passionate and dedicated colleagues, in an empowering environment, toward a global vision, striving for a future in which transformative molecular diagnostics can help millions of patients
Open, transparent culture that includes weekly Town Hall meetings
The ability to indirectly or directly change the lives of hundreds of thousands patients
Multiple medical benefit options
employee premiums paid 100% of select plans, dependents covered up to 80%
Extremely generous Family Bonding Leave for new parents (16 weeks, paid at 100%)
Supplemental fertility benefits coverage
Retirement savings program including a 4% Company match
Increase paid time off with increased tenure
Latest and greatest hardware (laptop, lab equipment, facilities)

Fulltime

Clinical Laboratory Technologist - Flow Cytometry

Are you motivated to participate in a dynamic, multi-tasking environment? Do you...

Location

United States , Aliso Viejo

Salary:

28.53 - 64.41 USD / Hour

NeoGenomics Laboratories

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Medical Technology from an accredited college or university preferred
Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences with the addition of at least one year of laboratory experience/training/training course
1+ years equivalent experience (high complexity testing) preferred
Certificate Compliance Requirements: ASCP certification for the assigned specialty, as available
FL: current state license to perform laboratory testing = Clinical Laboratory Technologist
CA: current state license to perform laboratory testing = Clinical Laboratory Scientist or Clinical Cytogeneticist Scientist or Clinical Genetic Molecular Biologist
TN: current state license to perform laboratory testing = Medical Laboratory Professional

Job Responsibility

Performs clinical laboratory tests proficiently in the department under general supervision, and exercises independent judgment in the specialty assigned
Follows the laboratory’s procedures for specimen handling and processing, test analyses, reporting and maintains accurate and complete records of all testing performed on-site
Maintains records that proficiency testing samples are tested in the same manner as patient specimens
Determines the acceptability of specimens for testing, prepares clinical specimens for testing and identifies specimen related problems according to established SOP guidelines
Analyzes specimens using approved testing procedures
Reviews, releases test results and follows department’s procedure in reporting STATS or Critical results to the interpreting physician per department SOP
Performs and documents Quality Control on reagents, equipment and assays. Recognizes and acts on QC failures by consultation or follow-up with the department Supervisor or Lead technologist regarding courses of action taken to achieve resolution
Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications
Prepare stock solutions, reagents and cocktails used in the laboratory as per established SOP’s. Tests and evaluates them based on standard criteria and documents all observed results

What we offer

Career development
Career coaches internally
Many training opportunities
Highly competitive benefits with a variety of HMO and PPO options
Company 401k match
Employee Stock Purchase Program
Tuition reimbursement
Leadership development
16 days of paid time off plus holidays
Wellness courses

Fulltime

Clinical Laboratory Technologist - Flow Cytometry

Are you motivated to participate in a dynamic, multi-tasking environment? Do you...

Location

United States , Fort Myers

Salary:

29.38 - 63.58 USD / Hour

NeoGenomics Laboratories

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Medical Technology from an accredited college or university preferred
Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences with the addition of at least one year of laboratory experience/training/training course
1+ years equivalent experience (high complexity testing) preferred
ASCP certification for the assigned specialty, as available
current state license to perform laboratory testing = Clinical Laboratory Technologist (FL)
current state license to perform laboratory testing = Clinical Laboratory Scientist or Clinical Cytogeneticist Scientist or Clinical Genetic Molecular Biologist (CA)
current state license to perform laboratory testing = Medical Laboratory Professional (TN)

Job Responsibility

Performs clinical laboratory tests proficiently in the department under general supervision, and exercises independent judgment in the specialty assigned
Follows the laboratory’s procedures for specimen handling and processing, test analyses, reporting and maintains accurate and complete records of all testing performed on-site
Maintains records that proficiency testing samples are tested in the same manner as patient specimens
Determines the acceptability of specimens for testing, prepares clinical specimens for testing and identifies specimen related problems according to established SOP guidelines
Analyzes specimens using approved testing procedures
Reviews, releases test results and follows department’s procedure in reporting STATS or Critical results to the interpreting physician per department SOP
Performs and documents Quality Control on reagents, equipment and assays. Recognizes and acts on QC failures by consultation or follow-up with the department Supervisor or Lead technologist regarding courses of action taken to achieve resolution
Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications
Prepare stock solutions, reagents and cocktails used in the laboratory as per established SOP’s. Tests and evaluates them based on standard criteria and documents all observed results

What we offer

Career development and empowering employees
Career coaches internally
Many training opportunities to expand knowledge base
Highly competitive benefits with a variety of HMO and PPO options
Company 401k match
Employee Stock Purchase Program
Tuition reimbursement
Leadership development
Start employees off with 16 days of paid time off plus holidays
Wellness courses

Fulltime

Clinical Laboratory Technologist

The Clinical Laboratory Technologist works under general supervision and is resp...

Location

United States , Aliso Viejo; Ft Myers; Tampa; Nashville; Houston; Carlsbad; Scottsdale; Durham; Ramsey

Salary:

28.53 - 64.41 USD / Hour

NeoGenomics Laboratories

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Medical Technology from an accredited college or university preferred
Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences with the addition of at least one year of laboratory experience/training/training course
1+ years equivalent experience (high complexity testing) preferred
ASCP certification for the assigned specialty, as available
For FL: current state license to perform laboratory testing = Clinical Laboratory Technologist
For CA: current state license to perform laboratory testing = Clinical Laboratory Scientist or Clinical Cytogeneticist Scientist or Clinical Genetic Molecular Biologist
For TN: current state license to perform laboratory testing = Medical Laboratory Professional

Job Responsibility

Performs clinical laboratory tests proficiently in the department under general supervision, and exercises independent judgment in the specialty assigned
Follows the laboratory’s procedures for specimen handling and processing, test analyses, reporting and maintains accurate and complete records of all testing performed on-site
Maintains records that proficiency testing samples are tested in the same manner as patient specimens
Determines the acceptability of specimens for testing, prepares clinical specimens for testing and identifies specimen related problems according to established SOP guidelines
Analyzes specimens using approved testing procedures
Reviews, releases test results and follows department’s procedure in reporting STATS or Critical results to the interpreting physician per department SOP
Performs and documents Quality Control on reagents, equipment and assays
Recognizes and acts on QC failures by consultation or follow-up with the department Supervisor or Lead technologist regarding courses of action taken to achieve resolution
Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications
Prepare stock solutions, reagents and cocktails used in the laboratory as per established SOP’s

What we offer

Career development
Career coaches
Training opportunities
Competitive benefits with HMO and PPO options
Company 401k match
Employee Stock Purchase Program
Tuition reimbursement
Leadership development
16 days of paid time off plus holidays
Wellness courses

Fulltime

Clinical Laboratory Technologist

Are you motivated to participate in a dynamic, multi-tasking environment? Do you...

Location

United States , Ft Myers; Tampa; Nashville; Houston; Aliso Viejo; Carlsbad; Scottsdale; Durham; Ramsey

Salary:

28.53 - 64.41 USD / Hour

NeoGenomics Laboratories

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Medical Technology from an accredited college or university preferred
Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences with the addition of at least one year of laboratory experience/training/training course
1+ years equivalent experience (high complexity testing) preferred
ASCP certification for the assigned specialty, as available
For FL: current state license to perform laboratory testing = Clinical Laboratory Technologist
For CA: current state license to perform laboratory testing = Clinical Laboratory Scientist or Clinical Cytogeneticist Scientist or Clinical Genetic Molecular Biologist
For TN: current state license to perform laboratory testing = Medical Laboratory Professional

Job Responsibility

Performs clinical laboratory tests proficiently in the department under general supervision, and exercises independent judgment in the specialty assigned
Follows the laboratory’s procedures for specimen handling and processing, test analyses, reporting and maintains accurate and complete records of all testing performed on-site
Maintains records that proficiency testing samples are tested in the same manner as patient specimens
Determines the acceptability of specimens for testing, prepares clinical specimens for testing and identifies specimen related problems according to established SOP guidelines
Analyzes specimens using approved testing procedures
Reviews, releases test results and follows department’s procedure in reporting STATS or Critical results to the interpreting physician per department SOP
Performs and documents Quality Control on reagents, equipment and assays
Recognizes and acts on QC failures by consultation or follow-up with the department Supervisor or Lead technologist regarding courses of action taken to achieve resolution
Documents all corrective actions taken when test systems deviate from the laboratory’s established performance specifications
Prepare stock solutions, reagents and cocktails used in the laboratory as per established SOP’s

What we offer

Career development and empowering employees
Career coaches internally
Many training opportunities to expand knowledge base
Highly competitive benefits with a variety of HMO and PPO options
Company 401k match
Employee Stock Purchase Program
Tuition reimbursement
Leadership development
Start employees off with 16 days of paid time off plus holidays
Wellness courses

Fulltime

Medical Laboratory Scientist II - Chemistry

Join a team that’s setting the standard for safety and quality. Every day as a Q...

Location

United States , Royal Oak

Salary:

Not provided

Quest Diagnostics

Expiration Date

Until further notice

Requirements

One (1) year full-time experience or training (high complexity testing) in a clinical laboratory setting
BS/BA in Medical Technology, Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990
Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)
United States-educated candidates must provide a detailed original transcript
Proven leadership and problem-solving skills
Must be detail-oriented, have the ability to work independently, establish work priorities and to handle several tasks simultaneously for maximum department efficiency
Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients
Communication skills necessary to handle telephone inquiries from clients
Ability to deal with client information in a confidential manner
Proficiency in Microsoft Office (Word, Excel and Outlook) and Laboratory Information Systems

Job Responsibility

Perform test procedures of moderate/high complexity requiring the exercise of independent judgement and responsibility in those specialties in which they are qualified
Must demonstrate proficiency in all areas of testing and be proficient troubleshooting all applicable instruments/procedures in the department
Provides support to the department in the areas of quality control, troubleshooting complex problems, customer support, instrument and equipment maintenance, staff training, process improvement and the completion of special projects as assigned
Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met
Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results
Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients
Ensure reagents/test kits have received dates, expiration dates and if applicable opened dates
Perform and document QC analysis to ensure accuracy of clinical data and proper instrument function. Make quality control decisions regarding the disposition of an assay or test
Responsible for informing supervisory personnel of all problems associated with the proper performance of test procedures
Report any actual or potential deviation from standard or accepted testing procedures and cooperate fully with any investigation of same

What we offer

Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
Best-in-class well-being programs
Annual, no-cost health assessment program Blueprint for Wellness®
healthyMINDS mental health program
Vacation and Health/Flex Time
6 Holidays plus 1 "MyDay" off
FinFit financial coaching and services
401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
Employee stock purchase plan
Life and disability insurance, plus buy-up option

Fulltime

Senior Laboratory Manager

Talentmark are recruiting for a Senior Laboratory Manager to join a Life Science...

Location

United Kingdom , Macclesfield

Salary:

70000.00 - 73000.00 GBP / Year

CK Group

Expiration Date

Until further notice

Requirements

Educated to PhD level ideally
Extensive experience in a high-throughput clinical DNA Sequencing laboratory
Experience with clinical assay development, process development and project management
Proven track record in team leadership, staff development and laboratory management
Strong background in Quality Assurance and Quality Control applications in clinical diagnostics
Detail-oriented, highly organized, with excellent verbal and written communication skills
Ability to troubleshoot technical applications and manage laboratory automation systems
Strong knowledge of quality control practices and regulations of UKAS, ISO 15189, CAP and other regulatory agencies

Job Responsibility

Oversee testing of clinical samples and supervise, mentor, and develop laboratory staff, including scientists, technicians and support personnel
Lead a high-throughput clinical genome sequencing laboratory, including technical troubleshooting, developing and writing operational procedures, setting laboratory key performance indicators and establishing quality metrics
Design and implement processes and procedures to ensure efficient turnaround times and accuracy of results and oversee daily laboratory operations, including workflow optimization, resource allocation and equipment maintenance
Prepare and manage laboratory budgets, monitor expenditures and optimize resource utilization
Ensure all processes comply with national regulations, organizational policies and accreditation requirements and maintain ISO 15189, CAP and other accreditation standards, including preparation for audits and inspections
Lead initiatives for process improvement and communicate effectively with internal and external stakeholders

Fulltime

Senior Laboratory Manager

CK Group are recruiting for a Senior Laboratory Manager to join a Life Sciences ...

Location

United Kingdom , Macclesfield

Salary:

70000.00 - 73000.00 GBP / Year

CK Group

Expiration Date

Until further notice

Requirements

Educated to PhD level ideally
Extensive experience in a high-throughput clinical DNA Sequencing laboratory
Experience with clinical assay development, process development and project management
Proven track record in team leadership, staff development and laboratory management
Strong background in Quality Assurance and Quality Control applications in clinical diagnostics
Detail-oriented, highly organized, with excellent verbal and written communication skills
Ability to troubleshoot technical applications and manage laboratory automation systems
Strong knowledge of quality control practices and regulations of UKAS, ISO 15189, CAP and other regulatory agencies

Job Responsibility

Oversee testing of clinical samples and supervise, mentor, and develop laboratory staff, including scientists, technicians and support personnel
Lead a high-throughput clinical genome sequencing laboratory, including technical troubleshooting, developing and writing operational procedures, setting laboratory key performance indicators and establishing quality metrics
Design and implement processes and procedures to ensure efficient turnaround times and accuracy of results and oversee daily laboratory operations, including workflow optimization, resource allocation and equipment maintenance
Prepare and manage laboratory budgets, monitor expenditures and optimize resource utilization
Ensure all processes comply with national regulations, organizational policies and accreditation requirements and maintain ISO 15189, CAP and other accreditation standards, including preparation for audits and inspections
Lead initiatives for process improvement and communicate effectively with internal and external stakeholders

Fulltime

Lead Clinical Laboratory Scientist

BillionToOne

Location:
United States , Union City

Category:
Health and Beauty

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 26, 2025

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