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

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

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 Scientist - Histology of Respiratory Diseases

Are you an experienced scientist ready to apply your skills in a diverse and dyn...

Location

Sweden , Mölndal

Salary:

Not provided

Randstad

Expiration Date

Until further notice

Requirements

Experienced scientist with a strong background in histology and related image analysis techniques with a specific focus on respiratory diseases
ideally complemented by some experience in pathology and pre-clinical drug discovery processes
excellent laboratory skills

Job Responsibility

Provide scientific expertise in a role that can impact patients’ lives
Actively take part in scientific discussions, gain input from others and be involved in multiple project meetings to present and discuss experimental plans and data
Be actively involved in experimental phase of histological analyses, with responsibility to coordinate, perform and evaluate experiments as well as drive the establishment of new techniques
Characterize and validate target expression and subsequent evaluation of engagement of the target by drug treatment in both patient and in vivo tissue samples
Independently assess and report data with a clear understanding of its reliability, interpretation of findings and draw appropriate conclusions with input from others

What we offer

Competitive salary
Benefits
Collective agreements
Consultant manager support
Varying and developing assignments
Large network
Many social activities

Fulltime

Senior Scientist, Diagnostic Assay Development

10x Genomics is establishing a diagnostics effort to translate our leading singl...

Location

United States , Pleasanton

Salary:

158400.00 - 214400.00 USD / Year

10x Genomics

Expiration Date

Until further notice

Requirements

Ph.D. in Molecular Biology, Genetics, Biochemistry, or a related field, or M.S. with equivalent industry experience
3+ years (Ph.D.), 5+ years (M.S.) of hands-on industry experience in molecular diagnostics or genomics assay development
Extensive, direct hands-on experience with 10x Genomics single-cell and/or spatial technologies, including troubleshooting and optimization
Demonstrated ability to independently adapt and refine published molecular biology protocols
Strong background in NGS workflows, including nucleic acid extraction, PCR/qPCR, and library preparation
Experience working with complex or low-input clinical samples (e.g., FFPE tissue, primary tumor material)
Experience with cell culture methods

Job Responsibility

Assay Development & Execution: Independently execute complex single-cell and spatial genomics workflows
Serve as a hands-on technical expert for 10x Genomics platforms
Systematically troubleshoot and optimize assay workflows
Adapt, refine, and extend published protocols
Design and execute feasibility studies
Process diverse and challenging clinical sample types
Analytical Validation & Documentation: Design and execute experiments supporting analytical validation
Generate, review, and maintain high-quality laboratory documentation
Analyze assay performance metrics and quality control data
Clearly present experimental data and scientific conclusions

What we offer

Equity grants
Comprehensive health and retirement benefit programs
Annual bonus program or sales incentive program
Generous time off
Competitive and comprehensive health benefits package
Family friendly policies like parental leave

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

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 Scientist, Early Formulation Science and Drug Delivery, Drug Product Design

This position will be reporting into the Early Formulation Science and Drug Deli...

Location

United States , La Jolla

Salary:

90900.00 - 151500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Recent PhD with 0-3 year post-doctoral experience, MS with 7+ years experience, or BS with 8+ years experience in Chemistry, Chemical Engineering, Physical Chemistry, Physics, Physical Organic Chemistry, Pharmaceutics, or Pharmaceutical Sciences
Experience working independently and collaboratively in a laboratory environment

Job Responsibility

Evaluate the physicochemical properties of potential small molecule drug candidates to inform a drug product formulation strategy and developability risk assessment
Design and develop fit for purpose and diagnostic traditional and enabled formulations for preclinical studies
Design, execute, and interpret the results of polymorph and salt screens for potential drug candidates related to stability, manufacturability, and bio-performance
Apply first principles understanding of thermodynamics and kinetic processes to dissolution and precipitation of drugs in biorelevant conditions and physical and chemical stability in the solid state
Work in cross-disciplinary teams and partner with subject matter experts in Medicinal Chemistry, Pharmacokinetics & Drug Metabolism, and Clinical Pharmacology departments to influence candidate selection and progression
Develop strategic collaborations with academic and industrial researchers for addressing gaps in fundamental or applied science related to the pharmaceutical sciences
Conduct novel research and present significant findings via internal and external presentations or publications

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 12.5% of the base salary
eligibility to participate in our share based long term incentive program
Relocation support available

Fulltime

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Senior Clinical Laboratory Scientist

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