Senior Clinical Laboratory Scientist Job at American Nursing Care (Redwood City)

Senior Clinical Laboratory Scientist

The Senior Clinical Laboratory Scientist will be responsible for performing mode...

Location

United States , Madison

Salary:

69000.00 - 122000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Associate degree in a laboratory science (chemical or biological science) or medical laboratory technology from an accredited institution or equivalent laboratory training and experience as defined: 60 semester hours or equivalent from an accredited institution that, at a minimum, includes either 24 semester hours of medical laboratory technology courses, OR 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology, and 12 semester hours of chemistry, biology or medical laboratory technology in any combination
3+ years of high complexity clinical testing experience in a clinical laboratory setting
Demonstrated strong professionalism and leadership skills
Demonstrated intermediate level project management skills
Demonstrated strong technical skills and professional working knowledge of job industry
Demonstrated ability to perform the Essential Duties of the position with or without accommodation
Authorization to work in the United States without sponsorship

Job Responsibility

Perform moderate and highly complex laboratory tests, procedures, and analyses according to the laboratory’s standard operating procedures with minimal supervision
Perform, review, and document laboratory quality control procedures
Identify potential problems, determine potential solutions, and take appropriate action in order to maintain a high level of quality in test processes and results
Achieve and maintain competency on laboratory tasks
Participate in research, validation, and/or implementation of new procedures and/or technologies
Maintain stringent standards for quality, by identifying, investigating, correcting, and documenting 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
Determine appropriate time allocation between daily test processing needs and project needs in a high quality, efficient and effective manner with minimal direction
Demonstrate and maintain effective communication with internal employees, managers, customers, and cross-functional teams
Model behaviors that promote high productivity, quality and maintaining TAT
Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

New

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

Senior Scientist, Research

The Senior Scientist, Research, with limited guidance from more experienced scie...

Location

United States , Madison

Salary:

109000.00 - 185000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Ph.D. in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position
or Master’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 4 years of related experience in lieu of a Ph.D.
or Bachelor’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 6 years of related experience in lieu of Ph.D.
3+ years of industry or academia experience in biology and/or chemistry
2+ years of experience in medical device/IVD, biotech, life science, or pharmaceutical industry
Demonstrated proficiency in molecular biology and/or biochemical techniques
Demonstrated proficiency in the principles of molecular biology, biochemistry, next-generation sequencing (NGS), genomics, and/or protein research
Working knowledge of statistical and mathematical methods in biology/genetics
including, but not limited to, statistical software, such as JMP
Strong understanding of GMP, ISO, and Quality Systems

Job Responsibility

Provide leadership to a team of junior research associates and scientists
Independently develop, plan, and conduct advanced research experiments, identify problems and discrepancies, analyze results, and identify and address trends in study data
Analyze research/experimental data, interpret the results, and provide insights into the next steps
Utilize and apply methods or technologies effectively and provide ideas for new techniques, when appropriate
Provide technical input and develop research plans, experimental outlines, and design
Prepare and provide information and data for scientific abstracts, industry conferences, project meetings, or publication
Generate, document, and communicate development plans for critical aspects of a project
Prepare and approve detailed technical procedures, protocols, and reports
Evaluate impact of nonconforming data to product or process
Maintain lab notebook in a clear, complete, and consistent manner, following all legal, ISO, and QSR requirements

What we offer

paid time off (including days for vacation, holidays, volunteering, and personal time)
paid leave for parents and caregivers
a retirement savings plan
wellness support
health benefits including medical, prescription drug, dental, and vision coverage
bonus eligible

Fulltime

Associate Scientist (Clinical Assay)

At Pfizer, our purpose is to deliver breakthroughs that transform patients' live...

Location

United States , Pearl River

Salary:

60200.00 - 97500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

BA/BS with 0 to 2 years of experience with laboratory in a relevant field of science, acquired in academic/industrial setting
Proficiency in computer skills, including word processing, Excel, PowerPoint, and relevant scientific software
Ability to collaborate and work effectively in a team environment
Strong problem-solving skills
Excellent communication skills
Strong attention to detail
Strong organizational skills
Ability to work independently and as part of a team
Ability to manage multiple tasks and projects simultaneously

Job Responsibility

Develop and conduct immunological assays to support vaccine clinical development, adhering to Good Clinical Laboratory Practice (GCLP) requirements
Present progress on assay development and sample analysis to colleagues and senior management
Collect and analyze data to support troubleshooting, qualification, and other lab projects
Provide critical data review of both clinical and nonclinical data
Execute sample testing and analysis for toxicology and clinical trials
Build team skills and collaborate effectively within the work group
Stay current on all departmental and corporate training
Organize work to meet deadlines and apply technical skills
Maintain a detailed inventory of freezer reagents, including controls, proficiency panels, toxins, and reference standards
Ensure timely preventive maintenance and proper care of qualified laboratory equipment, coordinating service requests, documenting activities, and maintaining equipment readiness to support uninterrupted assay operations

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation
holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
Relocation assistance may be available based on business needs and/or eligibility

Fulltime

Associate Scientist - Clinical Immunology

At Pfizer, our purpose is to deliver breakthroughs that transform patients' live...

Location

United States , Pearl River

Salary:

60200.00 - 97500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

BA/BS in Science with 0 - 2 years of relevant experience
Strong attention to detail
Ability to collaborate and work effectively in a team environment as well as independently
Proficiency in computer skills, including word processing, Excel, PowerPoint, and relevant scientific software
Experience in developing and troubleshooting bioassays designed to assess antibody functionality
Experience with mammalian cells and aseptic techniques

Job Responsibility

Conduct biofunctional immunological assays to support vaccine clinical development, adhering to Good Clinical Laboratory Practice (GCLP) requirements
Maintain a detailed inventory of freezer reagents, including controls, proficiency panels, toxins, and reference standards
Collect, analyze, and critically review clinical and nonclinical data to support assay development, sample analysis, troubleshooting, qualification, and other laboratory projects, and present progress to colleagues and senior management
Execute sample testing and analysis for toxicology and clinical trials, and provide critical review of resulting clinical and nonclinical data
Build team skills and collaborate effectively within the work group
Stay current on all departmental and corporate training
Organize work to meet deadlines and apply technical skills
Follow procedures for assigned tasks and seek guidance when necessary

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary
Relocation assistance may be available

Fulltime

Biomedical Scientist – Microbiology

We are excited to present an excellent opportunity for a Biomedical Scientist to...

Location

United Kingdom , Central London

Salary:

35000.00 - 50000.00 GBP / Year

Hunter Gatherer AHP

Expiration Date

Until further notice

Requirements

HCPC-registered Biomedical Scientist (Microbiology discipline)
Demonstrable post-registration experience in a UKAS-accredited Microbiology laboratory
Strong technical skills in clinical bacteriology, virology, or related disciplines
Experience using LIMS systems and handling sensitive patient data
Committed to teamwork, service excellence, and continuous improvement

Job Responsibility

Conduct routine and specialist diagnostic microbiology tests, including bacteriology, virology, parasitology, and mycology
Process a wide variety of clinical samples accurately and efficiently
Operate and maintain a range of microbiological laboratory equipment after competency training
Participate actively in internal and external quality assurance schemes
Support stock control, equipment evaluations, and method development initiatives
Adhere to laboratory policies, procedures, and UKAS accreditation requirements
Work collaboratively with senior biomedical scientists and multidisciplinary teams

What we offer

Contributory pension scheme (up to 20% total contribution)
Private medical healthcare
33 days annual leave (inclusive of bank holidays)
Season ticket loan and family-friendly benefits
Access to retail and service discounts
Clear career development pathways and training support

Fulltime

Senior Research Scientist (Pre-clinical) - 4DBio³ ODB

The Senior Research Scientist (Pre-clinical) serves as a scientific lead for pre...

Location

United States , Rockville

Salary:

135000.00 - 155000.00 USD / Year

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

Ph.D. in a relevant field (e.g., biology, pathology, biochemistry, bioengineering, molecular and cell biology, or genetics) required
3-5 years’ experience with planning and management of innovative medical and/or scientific research programs
Minimum 8 years direct experience in hematopoiesis research such as cell culture and differentiation of stem cells and/or synthetic blood substitutes
Experience with multi-color flow cytometry and cell sorting
Experience with blood cell function assays
Experience with gene editing and molecular biology techniques
Ability to design and execute in vitro experiments
Experience and success in writing and receiving federal research grants, cooperative agreements, and/or contracts
Experience working in DoD or other Federal research environments
Experience supervising research personnel

Job Responsibility

Perform recurring analyses on research portfolios to identify critical gaps, exceptional results and/or lack of progress
Assist in the preparation of SOPs and analysis of laboratory experiments
Prepare interim and final progress reports
Ensure research integrity
Disseminate research results
Provide guidance to scientists preparing research proposals, to include guidance on research protocol development, as needed
Maintain open communication with Principal Investigators and Center Leadership, advises of processes, reports progress, and serves as a point of contact, as applicable
Perform scientific reviews on research proposals submitted for consideration, as requested
Direct multifunctional teams and provides scientific domain expertise as needed
Adhere to Occupational Safety and Health Administration (OSHA), Good Laboratory Practices (GLP) and infection control procedures, as applicable

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year
up to 4 weeks of paid time off in a rolling year

Fulltime

Senior Clinical Laboratory Scientist

American Nursing Care

Location:
United States , Redwood City

Category:
Health and Beauty

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 17, 2026

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Job Posted:January 17, 2026

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January 17, 2026