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

Medical Laboratory Scientist I

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

Location

United States , Tucker

Salary:

30.00 USD / Hour

Quest Diagnostics

Expiration Date

Until further notice

Requirements

BS in Medical Technology preferred
or BS/BA in Chemistry or Biology
or Associates degree in a Laboratory Science or Medical Technology
or Previously qualified as a Technologist under 42 CFR 493
1 year Clinical experience (high complexity testing) preferred

Job Responsibility

Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result
Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens
Analyze specimens using approved testing procedures
Review and release test results
Follow CLIA, HIPAA, OSHA, and safety guidelines as described in their respective guidelines
Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance
Identify problems that may adversely affect test performance or reporting of test results, correct the problems encountered or immediately notify the senior technologist or supervisor

What we offer

$10,000 sign on bonus for eligible external candidate
Relocation assistance will be considered
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

Fulltime

New

Medical Laboratory Scientist Trainee

Medical Laboratory Scientist Trainee - Chantilly, VA, Tuesday to Saturday, 4:00 ...

Location

United States , Chantilly

Salary:

23.00 USD / Hour

Quest Diagnostics

Expiration Date

Until further notice

Requirements

BS/BA in Medical Technology, Chemistry or Biology, or qualifies as a Technologist under 42 CFR § 493.1489
Foreign educated candidates must provide a detailed credential evaluation from NACES or AICE
Ability to stand and work at the bench for long periods of time
Lifting and carrying objects up to 50 pounds
Frequent walking and/or standing
Manual dexterity for pipettes and laboratory instruments
Theoretical and operational job knowledge in designated specialty
Knowledge of organizational/departmental policies and procedures
Must be detail-oriented, ability to work independently, establish work priorities and handle several tasks simultaneously
Interpersonal skills to deal courteously and effectively with supervisors, co-workers and clients

Job Responsibility

Perform assigned analytical tests under the direction of senior laboratory personnel in accordance with SOPs ensuring quality control
Actively support and comply with laboratory policies and procedures
Adhere to analytical schedules to maintain turnaround time
Ensure test systems are 'in control'
Inform supervisory personnel of problems
Report deviations from standard procedures
Maintain laboratory areas and equipment in safe, functional, sanitary condition
Adhere to CLIA, HIPAA, OSHA, and laboratory safety requirements
Use personal protective equipment and engineering controls as directed
Other duties as assigned

What we offer

Day 1 Medical, supplemental health, dental & vision for FT employees working 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
401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months
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

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

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Senior Clinical Laboratory Scientist

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