Clinical laboratory scientist jobs in Laguna Niguel, CA

Qualifications: · High School Diploma; AS or BS strongly preferred · 1+ years of experience equivalent to an Accessioning Technician preferred · Proficient with MS Office programs · Ability to communicate effectively · Strong organizational skills and attention to detail · Ability to work independently · Must be able to work in a fast paced, multi-tasking environment and maintain production and quality standards · Must be able to work in a biohazard environment and comply with safety policies and standards outlined in the Safety Manual. · Willingness to work any shift which can include nights and weekends.

Department: Cardiac Cath Lab FLSA Status: Non-Exempt - 12 week Contract Shift: 8 hours, Days Join Premier Healthcare Staffing as a Certified Cath Lab Tech and step into a high-impact, day-shift contract where your expertise truly matters. You'll work alongside a skilled cardiovascular team, operate advanced technology, and play a vital role in delivering life-saving care-all within a supportive environment that values your experience. Enjoy competitive pay while elevating your career and making a difference from day one. EDUCATION, EXPERIENCE, TRAINING Requires previous experience assisting with scrubbing procedures in a Cardiovascular Lab. ARRT-R and license required Cardiovascular technician training program with emphasis in invasive cardiology and hemodynamic monitoring. BCLS (AHA) required upon hire and maintain current. Advanced Cardiac Life Support (ACLS); required. Proficient computer skills. Premiere Healthcare Staffing is here to help you on your career journey! We place talented candidates with our partner healthcare facilities with the shared goal of providing exceptional, compassionate care. Award-winning hospital partners across the nation Dedicated career specialists to support you every step of the way Immediate and flexible opportunities to create your career journey Tailored career pathway where you can thrive personally and professionally

Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Clinical Laboratory Scientist Supervisor to work for a leading Greater Orange County area biotechnology company. Salary: $120-150k/year depending on experience Summary:The Clinical Laboratory Scientist (Supervisor) is responsible for performing moderate or high complexity laboratory tests, as defined by CLIA, in microbiology and molecular testing. Directs, supervises, and coordinates functions and activities in all aspects of the clinical lab. Responsibilities: Oversee and ensure the overall functioning of the clinical laboratory, including managing workflow, scheduling staff, and ensuring timely completion of tests and procedures. Ensure that all clinical testing complies with safety and CLIA/CAP guidelines. Must be onsite to provide direct supervision when high complexity testing is performed by any individual. Maintain effective communication with the team on day-to-day activities and on-going projects. Train and provide orientation to all laboratory personnel; review all associated training documents; and perform all evaluations of testing personnel performances. Troubleshoot highly complex problems that can adversely affect test performance. Be familiar with laboratory protocols and procedures for specimen processing, operating equipment and instruments, and data analysis. Manage inventory of laboratory equipment, reagents, and supplies. Coordinate maintenance and calibration of laboratory instruments and equipment. Perform laboratory testing and analyze test results accurately and efficiently, ensuring the accuracy and reliability of laboratory data. Conduct/coordinate with internal and external audits and report instances of noncompliance. Participate in all Quality Assurance and Quality Improvement efforts. Plan and perform assay validations/verifications; write summary reports. Conduct competency assessments and proficiency testing per CAP/CLIA guidelines. Implement quality control measures and review QC/QA metrics at least monthly. Keep up to date with advancements in laboratory science through continuing education. Experience/Requirements: Must have an active California State license as a Clinical Laboratory Scientist (Generalist) Molecular testing and next-gen sequencing experience HIGHLY desired 3+ years of experience in Clinical Laboratory Science or related fields Please send resumes to *********************** and visit our website at ******************* for additional job opportunities!!!

At ScionHealth, we empower our caregivers to do what they do best. We value every voice by caring deeply for every patient and each other. We show courage by running toward the challenge and we lean into new ideas by embracing curiosity and question asking. Together, we create our culture by living our values in our day-to-day interactions with our patients and teammates. Job Summary Under general supervision, performs and reports routine and special laboratory tests on clinical specimens to aid in the diagnosis and monitoring of patients. Essential Functions * Performs analyses in hematology, chemistry, urinalysis, coagulation, blood bank and microbiology according to expected performance standards. * Performs venipuncture, finger stick, or heel stick on identified patients by physician's request in a timely, accurate and caring manner. * Keeps documented records current regarding maintenance and quality control. * 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 * 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 general supervisor, technical supervisor, clinical consultant, or director. * Follow the laboratory's established corrective action policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance. * Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications Knowledge/Skills/Abilities/Expectations * Comprehensive knowledge of applicable safety, quality control, and specimen handling guidelines and procedures. * Skilled in using applicable laboratory equipment such as centrifuges, meters, microscopes, incubators, pipettes, autoclaves, and sterilizers. * Ability to work quickly and accurately when under strict deadlines. * Considerable knowledge of the theory and practice of clinical laboratory methods and instrumentation. Working knowledge of anatomy, physiology, laboratory medicine, disease processes, and laboratory procedures. * Ability to maintain confidentiality of all patient and/or employee information to assure patient and/or employee rights are protected. * Must read, write and speak fluent English. * Must have good and regular attendance. * Approximate percent of time required to travel: 0% * Performs other related duties as assigned. Pay Range: $44.12-$55.95/hr. ScionHealth has a comprehensive benefits package for benefit-eligible employees that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness. Qualifications Education * Bachelor's degree in a chemical, physical, biological science, or medical technology from an accredited institution. Licenses/Certifications * Current license issued by the State in which the laboratory is located, if such licensing is required. * Certification as a Medical Technologist or Medical Laboratory Scientist by a nationally recognized agency/board preferred. Experience * 1-2 years of acute care hospital lab experience in high complexity testing preferred.

Pangea Laboratory is looking for a dynamic individual to join our team! The Clinical Lab Scientist is a licensed professional responsible for performing high-complexity clinical laboratory testing, with emphasis on Next Generation Sequencing (NGS) and assay validation, in accordance with Pangea's protocols and regulatory standards. This role maintains competency in all phases of testing (pre-analytic, analytic, and post-analytic), operates and troubleshoots automated laboratory instruments, and ensures accurate and timely entry of patient results into the laboratory information system. The Clinical Lab Scientist is accountable for real-time documentation of testing activities, quality control, preventive maintenance, and corrective actions when test systems deviate from established performance specifications. Working under the direction of the Laboratory Director (or designee), this position also supports the evaluation and implementation of new methods, contributes to the creation and revision of standard operating procedures, manages reagent and supply inventory, adapts to evolving workflows, and effectively communicates with management, auditors, clients, and internal teams. This role will be fully on-site in Tustin, CA with working hours M-F 10AM to 6:30PM. Join us in making a meaningful impact! Essential Duties and Responsibilities: Performs and maintains competency in all technical procedures (pre-analytic, analytic, and post-analytic) per Pangea's protocols and procedures. Operates automated laboratory instrumentation assigned to designated department and/or shift, including troubleshooting, preventive maintenance, calibration and repair procedures as required. Consistently and accurately transcribes patient test results from raw data generated from an instrument into the laboratory information system. Must have good reasoning ability; be knowledgeable of clinical pathology processes and use organizational skills to meet established turnaround time deadlines. Responsible for the accurate documentation of all testing activities including but not limited to patient specimens, proficiency testing, quality control results, performance of preventive maintenance/calibration of instruments, and LIS results entry. Capable of identifying problems that may adversely affect test performance or reporting of test results and either must correct the problem(s) or immediately notify the General Supervisor, Chief Operating Officer or Laboratory Director. Responsible for the documentation of corrective actions when test systems deviate from the laboratory's established performance specifications. Responsible for the inventory monitoring, labeling, and storing of incoming reagents and supplies. Maintains complete and documents records in real time that includes but is not limited to department logs, files, batch records, and work sheets. Participates in the evaluation of new methods and procedures under the direction of the Laboratory Director or designee. Adapts to changes in processes, accepting approved changes and learning new tasks. Responsible for the creating and revising standard operating procedures following all document control processes. Performs other related duties as required or assigned. Education and Experience: A minimum of two years of experience as an active licensed clinical laboratory scientist is preferred, including Next Generation Sequencing and assay validation. Minimum of a Bachelor's degree in a chemical, biological, clinical or medical laboratory science, or medical technology from an accredited institution. State of California license required; Generalist CLS license is preferred. Required Knowledge, Skills or Abilities: Knowledge of basic computer skills such as Microsoft Office Suite to include Excel and Word. Ability to read, analyze, and interpret such documents as pertaining to the performance and analysis of analytical testing. This could include but not limited to reagent package inserts, and standard operating procedures. Ability to effectively present information and respond to questions from management, clients, auditors and internal customers. About Us: Pangea Laboratory is a California-based diagnostics company founded in 2014. We focus on the precise, early detection of emerging diseases. Our mission is to have a positive impact on human life, by providing biomedical communities with reliable and high-quality testing services, delivering the data they need to diagnose and treat diseases in an effective and timely manner. Named a Top Workplace by the OC Register, Pangea Laboratory continues to be a place where employees feel engaged, connected, and energized about their work. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want to speak with you! Compensation, Benefits, and Perks: The estimated base compensation range for this position is $47 - $55 per hour at the time of posting. Actual compensation details will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. Pangea Laboratory also offers competitive benefits and perks including: Medical, Dental, Vision, and Life Insurance Coverages EAP Sessions Vacation Time plus Company Holidays Paid Sick Leave Generous 401(K) with matching Employee Referral Bonus Complimentary fruit, snacks, and beverages Complimentary catered lunches on Thursdays Equal Employment Opportunity Employer: Pangea Laboratory welcomes candidates of all backgrounds. These include sex, age, color, race, religion, marital status, national origin, ancestry, sexual orientation, gender, gender identity, gender expression, physical & mental disability, medical condition, genetic information, military and veteran status, or any other protected status as defined by federal, state, or local law. Location: Onsite - Pangea HQ, 14762 Bentley Circle, Tustin, CA 92780 Disclaimer: At Pangea Laboratory, we take the integrity of our hiring process seriously. Please be aware of fraudulent recruitment activities that may use our name to deceive job seekers. We will never ask for payment, sensitive personal information, or financial details during the recruitment process. All legitimate communications will come from an official Zymo or TriNet Hiring email address. If you are contacted by anyone claiming to represent us using a free email service (e.g., Gmail, Yahoo, Hotmail) or asking for payment, please treat this as fraudulent and report it immediately to ******************

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Licensed technologists must have a current & active license (California CLS Generalist). The technologist shall be proficient in assays/methodologies including, but not limited to: ABO typing, Nucleic Acid Testing, and serological assay (EIA, ELISA). The technologist is expected to execute both manual and automated test platforms. Primary Responsibilities Include: Follow laboratory procedures for handling and processing of sampling, test analyses, reporting and maintaining records of patient results. Follow prescribed procedures, performing any of the tests within any of the laboratory specialties. Calculate the results of the tests performed, if necessary. Accurately enter results of testing, as needed. Issue accurate test results, if trained. Operate, calibrate, conduct performance checks, and maintain laboratory analyzers or equipment, as necessary. Recognize and correct basic analyzer malfunctions. Notify supervision/management, when appropriate. Maintain adequate inventory of supplies, reagents and materials. Evaluate media, reagents, and calibrators according to established criteria. Prepare reagents and/or media as per prescribed procedure. Conduct established quality control procedures on analytical tests, equipment, reagents, media, and products. Evaluate results of quality control, and implement corrective action(s) when indicated. Review and follow Standard Operating Procedures (SOPs). Accept or reject test results in accordance with SOPs. Orient, mentor and/or teach new employees and/or employees that require cross-training on clinical laboratory methods, procedures and techniques. Adhere to all Quality Assurance, HIPAA and Safety standards. Adhere to all testing turnaround timelines. Meets basic expectations of DPT's quality management system, including, but not limited to good workmanship, adherence to standard operational procedures, training, good documentation practices, accurate recordkeeping so the company may meet its stated quality policy and objectives. Document all corrections and/or corrective actions when test systems deviate from the laboratory's established performance specification. Support Eurofins DPT's business philosophy, leadership values, and ethics. Represent laboratory and the organization favorable and in accordance with established Company standards and associate attributes at all times. Demonstrates a high level of integrity and honesty in performing tests, documenting test results and maintaining patient, client, employee and laboratory business confidentiality. Other duties as formally assigned by laboratory Management. Participate on special project teams a requested by laboratory Management. Qualifications Bachelor's (BA or BS) degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution. The appropriate State License to perform clinical laboratory testing in which the laboratory is located. In California, must be licensed by the State of California Department of Public Health. In Georgia, must successfully complete a certification examination from ASCP, AMT, NCA, or AAB. In Hawaii, must be licensed by the State of Hawaii to perform Histocompatibility and/or infectious disease testing. Employee must provide a current copy of license to laboratory Management. Responsible for maintaining licensure and continuing education as required per licensing agency and/or State. NOTE: License is mandatory for the role; the loss of licensure or failure to renew license will result in an unpaid of leave of absence or termination (to be determined by laboratory Management). Strong organizational and planning skills as well as strong keen attention to detail. Strong and effective written and verbal communication skills, and interpersonal/ teamwork skills. Intermediate or higher level of proficiency with computers; Proficiency in Microsoft Office Suite software programs including accurate keyboarding skills. Internal & External customer-centric Skills. WORK EXPERIENCE REQUIREMENTS Previous experience in Transplant Testing not required. General knowledge of assay theory and instrumentation. Knowledge of the principles, methods, materials, equipment, and techniques of medical technology. Knowledge of the principles of chemistry, biology, and bacteriology as related to medical technology. Some knowledge of recent developments in the field of medical technology. Ability to perform assigned tasks according to prescribed procedures. Ability to make accurate observations and records of tests results. Skill in the use of medical laboratory equipment. Additional Information What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Pay Range: $54 - $58 per hour Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Licensed technologists must have a current & active license (California CLS Generalist). The technologist shall be proficient in assays/methodologies including, but not limited to: ABO typing, Nucleic Acid Testing, and serological assay (EIA, ELISA). The technologist is expected to execute both manual and automated test platforms. Primary Responsibilities Include: Follow laboratory procedures for handling and processing of sampling, test analyses, reporting and maintaining records of patient results. Follow prescribed procedures, performing any of the tests within any of the laboratory specialties. Calculate the results of the tests performed, if necessary. Accurately enter results of testing, as needed. Issue accurate test results, if trained. Operate, calibrate, conduct performance checks, and maintain laboratory analyzers or equipment, as necessary. Recognize and correct basic analyzer malfunctions. Notify supervision/management, when appropriate. Maintain adequate inventory of supplies, reagents and materials. Evaluate media, reagents, and calibrators according to established criteria. Prepare reagents and/or media as per prescribed procedure. Conduct established quality control procedures on analytical tests, equipment, reagents, media, and products. Evaluate results of quality control, and implement corrective action(s) when indicated. Review and follow Standard Operating Procedures (SOPs). Accept or reject test results in accordance with SOPs. Orient, mentor and/or teach new employees and/or employees that require cross-training on clinical laboratory methods, procedures and techniques. Adhere to all Quality Assurance, HIPAA and Safety standards. Adhere to all testing turnaround timelines. Meets basic expectations of DPT's quality management system, including, but not limited to good workmanship, adherence to standard operational procedures, training, good documentation practices, accurate recordkeeping so the company may meet its stated quality policy and objectives. Document all corrections and/or corrective actions when test systems deviate from the laboratory's established performance specification. Support Eurofins DPT's business philosophy, leadership values, and ethics. Represent laboratory and the organization favorable and in accordance with established Company standards and associate attributes at all times. Demonstrates a high level of integrity and honesty in performing tests, documenting test results and maintaining patient, client, employee and laboratory business confidentiality. Other duties as formally assigned by laboratory Management. Participate on special project teams a requested by laboratory Management. Qualifications Bachelor's (BA or BS) degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution. The appropriate State License to perform clinical laboratory testing in which the laboratory is located. In California, must be licensed by the State of California Department of Public Health. In Georgia, must successfully complete a certification examination from ASCP, AMT, NCA, or AAB. In Hawaii, must be licensed by the State of Hawaii to perform Histocompatibility and/or infectious disease testing. Employee must provide a current copy of license to laboratory Management. Responsible for maintaining licensure and continuing education as required per licensing agency and/or State. NOTE: License is mandatory for the role; the loss of licensure or failure to renew license will result in an unpaid of leave of absence or termination (to be determined by laboratory Management). Strong organizational and planning skills as well as strong keen attention to detail. Strong and effective written and verbal communication skills, and interpersonal/ teamwork skills. Intermediate or higher level of proficiency with computers; Proficiency in Microsoft Office Suite software programs including accurate keyboarding skills. Internal & External customer-centric Skills. WORK EXPERIENCE REQUIREMENTS Previous experience in Transplant Testing not required. General knowledge of assay theory and instrumentation. Knowledge of the principles, methods, materials, equipment, and techniques of medical technology. Knowledge of the principles of chemistry, biology, and bacteriology as related to medical technology. Some knowledge of recent developments in the field of medical technology. Ability to perform assigned tasks according to prescribed procedures. Ability to make accurate observations and records of tests results. Skill in the use of medical laboratory equipment. Additional Information What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Pay Range: $54 - $58 per hour Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.

LetsGetChecked is a global healthcare solutions company that provides the tools to manage health from home through health testing, virtual care, genetic sequencing, and medication delivery for a wide range of health and wellness conditions. LetsGetChecked's end-to-end model includes manufacturing, logistics, lab analysis, physician support, and prescription fulfillment. Founded in 2015 and co-headquartered in Dublin and Atlanta, LetsGetChecked empowers people to take control of their health and live longer, happier lives. Priva Path Labs, a trusted partner of LetsGetChecked, is seeking a highly motivated and skilled Clinical Laboratory Scientist (CLS) to join our high-complexity laboratory team. This role is crucial for ensuring the accuracy, quality, and regulatory compliance of patient testing across multiple analytical platforms. The ideal candidate possesses a valid California CLS license and a strong commitment to maintaining scientific rigor and accountability that exceeds regulatory governance requirements. Responsibilities Core Laboratory Operations & Execution Perform all high-complexity patient testing that is authorized by the Laboratory Director, strictly following the laboratory's Standard Operating Procedures (SOPs). Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting, and maintaining records of patient results. Adhere to the laboratory's Quality Control policies and accurately document all QC activities, instrument and procedural calibrations, and routine maintenance. Ensure that all testing is performed in compliance with federal (CLIA) and state regulatory and quality standards. Quality Management & Compliance Maintain records demonstrating that Proficiency Testing (PT) samples are tested in the same manner as patient specimens (no inter-laboratory communication). Be capable of identifying problems that may adversely affect test performance or reporting and promptly correcting the issue or notifying the appropriate supervisor. Follow the laboratory's established policies, including taking and documenting corrective actions, whenever test systems are not within the laboratory's established acceptable levels of performance. Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications. Professionalism and Teamwork Maintain effective communication skills, working collaboratively as a team player. Be capable of working independently and multitasking in a fast-paced environment. Perform other duties as assigned. Qualifications and Skills Required Qualifications Education: Bachelor's degree in Medical Technology or a related life science (e.g., Biology, Molecular Biology, Genetics, Microbiology, Chemistry, or Biochemistry). Licensure: Valid California CLS license (either Generalist or Clinical Chemistry Scientist license is required). Experience: At least one year of experience in a high-throughput clinical laboratory performing high complexity testing. Preferred Qualifications Experience with automated liquid handling platforms is a plus. Experience with mass spectrometry (e.g., LC-MS/MS, GC-MS) or related analytical instrumentation is desirable. Experience with Sciex mass spectrometers is a plus. Strong organizational and time management skills. Must exhibit superb attention to detail and ethical behavior. Benefits: Alongside base salary of $53-$55.50 per hour, this position is eligible for a $10,000 signing bonus + 15% differential for second shift, we offer a range of benefits including: Health, dental & vision insurance 401k Matching contribution Employee Assistance Programme Annual Compensation Reviews LetsGetChecked has a flexible PTO policy 3 paid volunteer days per year Free monthly LetsGetChecked tests as we are not only focused on the well being of our patients but also the well being of our teams A referral bonus programme to reward you for helping us hire the best talent Internal Opportunities and Careers Clinics to help you progress your career Maternity, Paternity, Parental and Wedding leave #LI-Onsite Why LetsGetChecked At LetsGetChecked, we are revolutionizing healthcare by making it more accessible, convenient, and personalized. Our mission is to empower individuals with the knowledge and tools they need to manage their health proactively, so they can live longer, happier lives. By joining our team, you will be part of a dynamic and innovative company that is dedicated to improving lives through cutting-edge technology and compassionate care. We value our employees and invest in their growth, offering opportunities for professional development and career advancement. Together, we can make a meaningful impact on the future of healthcare and help people take control of their health journey. Join us in our commitment to transforming healthcare for the better. Our Commitment to Diversity, Equity, and Inclusion At LetsGetChecked, we are committed to fostering an inclusive environment that celebrates diversity in all its forms. We believe that the diversity of thought, background, and experience strengthens our teams and drives innovation. We are an equal-opportunity employer and do not discriminate on the basis of race, ethnicity, religion, color, place of birth, sex, gender identity or expression, sexual orientation, age, marital status, military service status, or disability status. Our goal is to ensure that everyone feels valued and empowered to thrive. Please review our Candidate Privacy Policy. To learn more about LetsGetChecked and our mission to help people live longer, healthier lives please visit ***************************************

Job Summary and Responsibilities Clinical Laboratory Scientist - St. Bernardine Medical Center At St. Bernardine Medical Center, every role contributes to our mission of delivering exceptional, compassionate care to the community we serve. We are seeking a skilled Clinical Laboratory Scientist (CLS) to join our laboratory team in performing essential diagnostic testing that supports patient care and clinical decision-making. In this role, you will apply the principles of fundamental sciences to analyze human specimens, providing accurate and timely results that guide diagnosis, treatment, and disease management. You will ensure that all testing meets the highest standards of quality and compliance, while working collaboratively with other healthcare professionals to support the needs of our patients. Key Responsibilities * Receive and evaluate clinical specimens, ensuring quality and adherence to testing protocols. * Perform qualitative and quantitative testing following approved policies and procedures. * Review test results for accuracy, medical relevance, and compliance before releasing reports. * Communicate critical values promptly and document actions taken. * Perform quality control, instrument maintenance, and troubleshooting as required. * Maintain reagent inventory and participate in proficiency surveys. * Assist in training and orienting new staff to laboratory operations. * Participate in quality improvement initiatives and remain current with departmental updates, policies, and procedures. Why Join Us? As a CLS at St. Bernardine Medical Center, you will be an integral part of the diagnostic process, directly impacting patient outcomes. We offer a supportive, team-focused environment, professional development opportunities, and the chance to work with advanced laboratory technology while contributing to our mission of excellence in care. Job Requirements * One year experience working as a generalist in an acute hospital clinical laboratory * State of California Clinical Laboratory Scientist License * Bachelor's Degree in a biological or chemical science as defined by CLIA. Where You'll Work Founded as a faith-based hospital in 1931 by the Sisters of Charity of the Incarnate Word, Dignity Health - St. Bernardine Medical Center is a 342-bed, acute care, nonprofit hospital located in San Bernardino, California. The hospital offers a full complement of services, including the Inland Empire Heart and Vascular Institute, an award-winning orthopedics program, surgical weight loss, and is an official Neurovascular Stroke Center, as designated by ICEMA. The hospital shares a legacy of humankindness with Dignity Health, one of the nation's five largest health care systems. Visit here ***************************************************************** for more information. One Community. One Mission. One California

Arrowhead Regional Medical Center (ARMC) is recruiting for Clinical Laboratory Scientist III. Positions in this series perform laboratory procedures and analyses in either a Public Health or Medical Center clinical laboratory. Clinical Laboratory Technologist III serve as lead supervisors and/or perform the most difficult tests which may be new or may involve many alternatives or procedural steps not necessarily covered by written instructions. The eligible list created from this recruitment may be used to fill other vacancies as they occur. For more information, refer to the Clinical Laboratory Scientist III job description. We are also accepting applications for Clinical Laboratory Scientist I and Clinical Laboratory Scientist II. Applicants are encouraged to apply for the appropriate level. EXCELLENT BENEFITS & RETIREMENT To review job- specific benefits, refer to: Summary of Benefits Memorandum of Understanding (MOU) CONDITIONS OF EMPLOYMENT Shift Availability: ARMC is a twenty-four-hour facility; some shifts include weekends and holidays. Applicants must indicate availability for day, swing, night, rotating, weekends, and holidays. Shift differentials are provided. Pre-Employment Process: Applicants selected for these positions must pass a background investigation, physical, and verification of employment history and education. Work Environment: Incumbents are routinely exposed to dangerous chemicals and infectious materials. Please note: San Bernardino County is not able to consider candidates who will require visa sponsorship at the time of application or in the future. Experience: Three (3) years of clinical laboratory experience as a Clinical Laboratory Technologist, that includes one (1) year of experience in an acute care hospital. * AND- License: Must possess and maintain a Clinical Laboratory Scientist license issued by the State of California Department of Public Health. Note: a limited license is not considered qualifying; license must include "MTA" prefix. Application Procedure: Applications will be accepted until a sufficient number of qualified applications are received. To receive priority consideration for this excellent opportunity, please complete and submit the online employment application and supplemental questionnaire as soon as possible. Resumes will not be accepted in lieu of the application and/or supplemental questionnaire. There will be a competitive evaluation of qualifications based on the information provided in your Application and the Supplemental Questionnaire. The most highly qualified candidates, based on the evaluation results, will be referred for an interview. Be sure to include in your application and supplemental questions your experience in meeting the minimum requirements. All communications regarding the selection process will be via e-mail. Applicants are encouraged to check their e-mail frequently to learn additional information regarding this recruitment. Check your GovernmentJobs account for notifications. Update your firewalls to allow e-mails from San Bernardino County through governmentjobs.com. Update your Spam, Junk, and Bulk settings to ensure it will not spam/block/filter communications from e-mail addresses with the following domain "@hr.sbcounty.gov". Finally, be sure to keep your personal information updated. Taking these steps now will help ensure you receive all communications regarding this recruitment. To ensure timely and successful submission of your online application, please allow ample time to complete and submit your application before the posted filing deadline. Applicants will be automatically logged out if they have not submitted the application and all required materials prior to the posted deadline. Once your application has been successfully submitted you will receive an onscreen confirmation and an email. We recommend that you save and/or print these for your records. If you require technical assistance, follow this link to review the Government Jobs online application guide, or contact their Toll-Free Applicant Support line at **************. Please note that Human Resources is not responsible for any issues or delays caused by the computer or browser used to submit the application. EEO/ADA: San Bernardino County is an Equal Employment Opportunity (EEO) and Americans with Disabilities Act (ADA) compliant employer, committed to providing equal employment opportunity to all employees and applicants. ADA Accommodation: If you have a disability and require accommodations in the testing process, submit the Special Testing Accommodations Request Form within one week of a recruitment filing deadline. Veterans' Preference: Eligible veterans and their spouses or widows/widowers who are not current County employees may receive additional Veterans' Preference points. For details and instructions on how to request these points, please refer to the Veterans' Preference Policy. For more important details, review the Applicant Information and County Employment Process.

Clinical Laboratory Scientist Job Number: 1323334 Posting Date: Dec 3, 2024, 7:56:46 PM Description Job Summary: Performs pre-analytical, analytical and post-analytical phase testing of all complexities as defined by Clinical Laboratory Improvement Act/Amendment (CLIA) to include specialized tests and analysis in one or more areas of clinical laboratory such as Hematology, Microbiology, Clinical Chemistry, Urinalysis, Immunohematology, Serology, Parasitology and chemical and morphological examinations to obtain data for use in diagnosis and recording laboratory test results. Analysis of test results are performed on the population serviced (e.g., neonatal, pediatric, adolescent, adult, geriatric clients). Note: FOR CLS WORKING AT THE RRL, SEE ADDITIONAL REQUIREMENTS SPECIFIED IN THE MINIMUM REQUIREMENT SECTION.Essential Responsibilities: Upholds Kaiser Permanentes Policies and Procedures, Principles of Responsibilities and applicable state, federal and local laws. Provides the highest level of patient care as defined by established standards and maintains confidentiality on all tests performed by the laboratory. Performs and reports test results for all clinical laboratory procedures as assigned, both automated and manual, in the clinical laboratory department, without immediate review by the director, consultant, or supervisory team. Demonstrates proficiency, competency and understanding of fundamental principles of clinical laboratory procedures with minimal amount of supervision. Monitors and is accountable for test data, quality control, quality assurance, preventive maintenance, proficiency testing and all operations related to laboratory testing procedures. Notifies Supervisory team of any irregularities of factors, which may influence test results. Ability to troubleshoot equipment and test methods. Identifies and resolves unusual laboratory situations and notifies appropriate parties within shift. Consults with physicians, nurses, pharmacists, etc. on the technical aspects of methodologies used, appropriateness of test utilization and interpretation of patient results. Instructs new employees and/or Clinical Laboratory Scientist students in laboratory procedures within area the CLS assigned, in order that they may develop proficiency and understanding of the clinical laboratory methodology. Provides training, guidance and pertinent technical information to Laboratory Assistants, support staff, clerks, CLS students and Medical Center personnel. Discusses clinical laboratory problems of mutual interest with the Supervisory team, and lead technologist in order to develop a better communication link within the department. Participates in work groups to work through problems, issues or goals of the department. Assists in evaluating new tests procedures when requested and communicates to the Supervisory team the possibilities for their implementation. Meets states requirements for mandatory CEUs. As defined by established standards, works in a professional, cooperative and courteous manner. Observes all laboratory, Kaiser Permanente and regulatory agency policies and procedures. Maintains overall safety (including chemical and biological) of the department in accordance with established safety, infection control and procedure protocols. Monitors supplies and reagents and notifies appropriate parties of par levels. As necessary and appropriate, may perform any clerical or other duties of support staff/laboratory assistants that may be assigned such as performing phlebotomy on inpatients and outpatients. Accepts responsibility of assisting in work areas not primarily his/her own. Operates computerized laboratory data systems/applications. Participates in direct patient care by providing the patient with information to enhance the understanding of laboratory test, instructing the patient on specimen requirements and conditions for specialized testing and collecting from the patient samples to include blood, body fluids, secretions, and tissues for analysis. Qualifications Basic Qualifications: Experience N/A. Education High School Education or General Education Development (GED) required. License, Certification, Registration Clinical Laboratory Scientist License (California) Additional Requirements: A Clinical Laboratory Scientist with a limited license will only qualify for a CLS position within their specialty and only applicable in the following departments at the Regional Reference Laboratories: Chemistry limited license qualifies for Automated Chemistry or Esoteric Chemistry CLS positions; Toxicology limited license qualifies for Esoteric Chemistry CLS positions; Immunology limited license qualifies for Molecular or Immunology CLS positions; Microbiology limited license qualifies for Bacteriology, Molecular or Immunology CLS positions; Hematology limited license qualifies for Hematology and Special Coagulation. Ability to demonstrate knowledge of and to utilize the principles, theories, practices, methodologies and techniques required of a Clinical Laboratory Scientist. NOTE: ADDITIONAL REQUIREMENTS FOR REGIONAL REFERENCE LABS (RRL): Function competently as a Licensed Clinical Laboratory Scientist in a high-volume Laboratory demonstrating knowledge of principles, theories, practices, techniques. Must have good communication skills and able to solve problems. And, as appropriate for the department/specialty, within the last three (3) years, at least six (6) months experience: Note: CLS students one (1) year internship can be considered meeting the experience requirement below. Experience in automated instrumentation; knowledge testing principles; molecular based procedures; QC protocols; knowledge in auto verification, EIA, chemiluminence and IFA platforms. Knowledge of method validations, and hematology validation, QC and calibration, manual diff count. (CORE LAB, includes AUTO CHEM, IMMUNOLOGY, HEMATOLOGY). Experience and knowledge in using high complex methods employing electrophoresis, chromatography, and mass spectrometry, and Special Coagulation (SPECIAL CHEMISTRY, SPECIAL COAGULATION, BIOCHEMICAL GENETICS). Read, interpret, work-up and report culture results for all areas of Aerobic and Anaerobic Bacteriology; proficient in reading and interpreting stained smears; knowledge and ability to set-up and report automated/molecular identification and susceptibility testing and interpret results (BACTERIOLOGY). NOTE: ADDITIONAL REQUIREMENTS FOR REGIONAL FLOW CYTOMETRY (LOS ANGELES): One (1) year recent experience in Flow Cytometry analysis such as leukemia / lymphoma phenotyping, paroxysmal nocturnal hemoglobinuria, T cell subset enumeration, DNA cell cycle analysis and cytochemical staining. Preferred Qualifications: One (1) year recent experience as a CLS. Notes: Days and hours may vary. Must be available to work weekends and holidays. Will work overtime according to collective bargaining agreement. Primary Location: California-Downey-Downey Medical Center Regular Scheduled Hours: 40 Shift: Night Working Days: Mon, Tue, Wed, Thu, Fri, Sat, Sun Start Time: 11:00 PM End Time: 07:30 AM Job Schedule: Full-time Job Type: Standard Employee Status: Regular Job Level: Individual Contributor Job Category: Laboratory Public Department Name: Downey Medical Center - Pathology/Lab-PermLab SysCoord - 0806 Travel: No Employee Group: B02-L324|UFCW|Local 324 Posting Salary Low : 54 Posting Salary High: 58.41 Kaiser Permanente is an equal opportunity employer committed to a diverse and inclusive workforce. Applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), age, sexual orientation, national origin, marital status, parental status, ancestry, disability, gender identity, veteran status, genetic information, other distinguishing characteristics of diversity and inclusion, or any other protected status.Click here for Important Additional Job Requirements. Share this job with a friend You may also share this job description with a friend by email or social media. All the relevant details will be included in the message. Click the button labeled Share that is next to Submit.

available near Avalon, California! The Clinical Lab Scientist is responsible for planning, evaluating, coordinating, and supervising laboratory personnel and daily operations to ensure quality patient care. The candidate conveys a positive image of the clinic and exhibits values of respect, integrity, innovation, and compassion. Details - Full-time and permanent - Shifts: Discussed during interview - Opportunities for growth - Full, comprehensive benefits package (PTO, health insurance, life insurance, 401k, etc) - 3 months free housing! Requirements - College degree - ASCP certification - CA license - Prior experience and knowledge Click apply or email your resume to leah@ka-recruiting.com/ call or text 617-746-2751! You can also schedule a time to chat here -https://calendly.com/leahkarecruiting/10min. REF#LM1445

Clinical Laboratory Scientist, Generalist Garden Grove, CA · Healthcare Job Title: Clinical Laboratory Scientist, Generalist (Graveyard Shift) Position Type: Full-Time, Graveyard Shift (11 PM - 7 AM) About Us: Our client is seeking a director hire and is dedicated to providing accurate, timely, and high-quality diagnostic testing services to improve patient outcomes. As a leading reference laboratory, we are committed to excellence in healthcare and are looking for experienced professionals to join our team. Job Summary: We are seeking a highly skilled and experienced Clinical Laboratory Scientist to join our dynamic team. This position requires a professional with at least five years of experience in a hospital laboratory setting, now seeking to broaden their impact in a reference lab environment. The successful candidate will be responsible for performing a variety of diagnostic testing and laboratory procedures during the graveyard shift from 11 PM to 7 AM. Key Responsibilities: Conduct complex chemical, biological, hematological, immunologic, microscopic, and bacteriological tests. Process and analyze specimens, interpreting and recording test results, and ensuring the accuracy and reliability of data. Operate, calibrate, and maintain equipment and instruments used in quantitative and qualitative analysis, such as spectrophotometers, calorimeters, flame photometers, and computer-controlled analyzers. Identify abnormal or atypical test results and follow appropriate corrective procedures to address such findings. Maintain and update professional knowledge and proficiency through continuing education, staff meetings, workshops, and participation in professional groups. Adhere to established laboratory safety guidelines and maintain a clean and safe work environment. Assist in the development and implementation of new testing procedures to enhance lab efficiency and accuracy. Collaborate with other laboratory staff and departments to ensure seamless lab operations and high-quality patient care. Provide mentorship and guidance to junior laboratory staff. Qualifications: Bachelor's degree in Medical Technology, Clinical Laboratory Science, or a related field. Valid certification as a Clinical Laboratory Scientist/Medical Technologist from a recognized certifying agency (ASCP). Minimum of five years of clinical laboratory experience, preferably in a hospital lab setting. Proficient in using laboratory information systems (LIS) and understanding of quality control principles and regulations. Excellent analytical, organizational, and communication skills. Ability to work independently and as part of a team, particularly during non-standard hours. What We Offer: Competitive compensation package. Comprehensive benefits including health, dental, vision, and life insurance. Opportunities for professional growth and development. A collaborative and supportive work environment.

Job DescriptionSalary: $50 - $58 Job Title:Clinical Laboratory Scientist (Generalist) Company:Monarch Diagnostics Job Type:Full-Time, In-PersonAbout Monarch Diagnostics: Monarch Diagnostics is a premier diagnostic testing laboratory based in Irvine, California. We specialize in high-complexity urine analysis, infectious disease testing, and drug screening services. Our mission is to deliver precise, reliable results that empower healthcare providers and improve patient outcomes. We partner with addiction recovery centers, mental health treatment facilities, and healthcare organizations nationwide.At Monarch, we believe in collaboration, integrity, and continuous growth. Our culture emphasizes teamwork and inclusion where every department works together to support our shared goal of advancing diagnostic excellence. If youre looking for a company that values both professional expertise and personal development, Monarch Diagnostics is the place to grow your career.Position Overview: Monarch Diagnostics is seeking afull-time, in-person Clinical Laboratory Scientist (Generalist)to join our dynamic team. This role involves performing and reviewing high-complexity tests, including LC/MS urine confirmations and infectious disease assays, in a fast-paced, CLIA-certified laboratory. The ideal candidate is detail-oriented, organized, and committed to maintaining high standards of accuracy and compliance.Youll work closely with our technical and quality teams to ensure testing integrity, troubleshoot issues, and help optimize laboratory workflows. This position offers opportunities for continued training, cross-departmental collaboration, and potential career advancement as Monarch expands its testing services.Key Responsibilities: Perform high-complexity clinical testing, including LC/MS urine confirmations and infectious disease assays, in accordance with SOPs and CLIA regulations Analyze, review, and validate test results prior to release to ensure accuracy and precision Conduct and document quality control procedures and participate in quality improvement activities Assist with test method development, validation, and verification as needed Maintain accurate records, logs, and documentation in compliance with regulatory standards Ensure adherence to laboratory safety protocols, PPE requirements, and HIPAA regulations Collaborate with laboratory management and technical staff to resolve operational and analytical issues Support training of new staff or students as assigned Contribute to maintaining a positive and collaborative team environment Qualifications: Bachelors degree in chemical, physical, biological, or clinical laboratory science, or medical technology from an accredited institution Valid California CLS license required Minimum of 2 years of experience working in a CLIA-certified clinical laboratory Experience in toxicology and LC/MS instrumentation preferred Strong understanding of laboratory quality systems and regulatory standards (CLIA, CAP, COLA, etc.) Excellent attention to detail, organizational, and problem-solving skills Strong written and verbal communication skills Proficiency with Microsoft Office, Google Workspace, and laboratory information systems (LIS) What We Offer: Competitive compensation commensurate with experience Health, dental, and vision benefits (for eligible employees) Supportive, team-based work culture Opportunities for advancement as the company grows Ongoing training and professional development opportunities

Job Description PRINCIPLE DUTIES AND RESPONSIBILITIES Responsible for ensuring that the test(s) requested by physicians and facilities are performed in an accurate and timely manner and the Laboratory policies and procedures are followed and implemented correctly. Follows the laboratory's procedures for specimen handling and processing analysis, reporting and maintaining records of patient test results. Ensuring that the patient's name and specimen number are correctly identified. Type of specimen and time drawn is correct for the test ordered. Specimen integrity has been maintained from the initial draw / pick-up of specimen(s) until arrival and completion of test(s) requested. Follows the laboratory's procedures for handling potentially infectious materials. Maintains records that demonstrate that proficiency testing samples are tested in the same manner as patient samples. Adheres to the laboratory's quality control policies, documents all quality control activities instrument and procedural calibrations and maintenance performed. Follows the laboratory's quality control policies whenever test systems are not within the laboratory's established levels of performance. Capable of identifying problems that may adversely affect test performance or reporting of test results. Documents all corrective action taken when test systems deviate from the laboratory's established performance specifications. Documents all corrective action taken when test systems deviate from the laboratory's established performance specifications. Performs all routine and new test procedures that are complex and require professional judgment when assigned to a specific area. Demonstrates knowledge of theory behind the test performed. Recognized departure from the norm on adult and geriatric patients and be able to understand the scientific and theoretical reasons for such deviation. Calibrates instruments and assess the accuracy of the equipment; performs equipment preventive and corrective maintenance. Check and verify all the test results released by the laboratory. This includes accepting or rejecting results due to delta check inconsistencies, requesting redraw for verification, canceling results due to gross hemolysis, clots or QNS. Reviews outgoing reports for technical and clerical errors. Able to communicate with nurses and physicians, and ability to work well with others. Assist the Lead CLS in maintaining adequate supplies and inventory levels. Demonstrates the ability to prioritize work duties. Recognizes the administrative changes in staffing and scheduling and adapt to these changes. Assists in developing and installing quality control standards to ensure accuracy of test results. Assists the Lead CLS in reviewing and solving quality control problems. Initiates, suggests and if necessary, implements technical and administrative changes upon approval of the Laboratory Director. EXPERIENCE / SKILLS REQUIRED Bachelor's degree from an accredited college or university with major coursework in medical technology, microbiology, chemistry, biology or related field. Possession of Clinical Laboratory Scientist's license issued by the State of California or equivalent license approved by LFS (Laboratory Field Services). Must meet CLIA requirements for testing personnel for High Complexity Testing. Have documentation of training, knowledge and experience in the department(s) assigned (Microbiology, Hematology, Chemistry and / or Immunology) to work. Have the necessary language reasoning and mathematical skills to follow and implement the laboratory policies and procedures approved by the Laboratory Director. Ability to work independently and have good sound analytical judgment to function effectively under stress in certain situations. Strong interpersonal skills sufficient to work closely with others on a team. Possess the ability to work in a fast paced environment, effectively interacting with physicians, facilities and laboratory personnel. Possess speed, consistency and accuracy in tasks to meet the laboratory standards. Customer service oriented Self starter with a high initiative, a good problem and decision-maker. Ability to demonstrate flexibility in work environment, performing a variety of changing tasks. Commitment to tasks. Displaying a high level of cognitive, interpretive or judgment skills.

Job Description Saving Lives with Early Detection Join Our Team as a Clinical Lab Scientist! We are seeking a dedicated Clinical Laboratory Scientist specializing in Molecular Genetics to join our dynamic team. As a key member, you will be responsible for conducting molecular genetics testing, ensuring quality control, and maintaining laboratory records. If you are passionate about molecular biology techniques and thrive in a fast-paced environment, we want to hear from you. Duties and Responsibilities: Perform DNA or RNA extraction from various biological samples. Quantify and qualify DNA and RNA using spectrophotometers and other techniques. Conduct molecular biology techniques including PCR, RT-PCR, and NGS. Adhere to CLIA and CAP guidelines. Prepare results using manual and computerized procedures. Maintain records demonstrating proficiency testing. Adhere to quality control policies and document all activities. Identify and correct problems that may affect test performance. Monitor TAT (Turnaround Time) and workflow. Assist in validation documentation of new tests and procedures. Order supplies and validate equipment and reagents. Report problems concerning cases, tests, equipment, and supplies. Qualifications/Requirements: Bachelor's degree in Medical Technology or Biological Science. Current California Clinical Laboratory Scientist (CLS) Generalist license. Or Current California Genetics Molecular Biology Scientist (CGMBS) license. Proficiency in Nucleic Acid Extraction, Amplification, and Sequencing. Skills: Excellent verbal and written communication skills. Ability to prioritize, work under pressure, and handle multiple tasks. Strong attention to detail and accuracy. Good tactile ability for delicate assembly work. Hardware/Software Experience: Proficient in Microsoft Office Suite (Word, Excel, PowerPoint). Experience with using Laboratory Information System (LIS) Experience using bioinformatics software for data analysis. Familiarity with Microsoft Teams for communication and presentations. Note: All applicants will be required to pass an onsite Pipette test. HOURLY RATE: $40 - $50 If you are a dedicated professional looking to make a difference in the field of molecular genetics, we encourage you to apply. Join us and contribute to cutting-edge research and innovation in healthcare.

Clinical Laboratory Scientist I - Hematopathology - (10032715) Description Clinical Laboratory Scientist I - HematopathologyJoin the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. We have an exciting Hematopathology Laboratory opportunity for a Clinical Laboratory Scientist I position at City of Hope, located in Duarte, California. This is a full-time position that welcomes new licensed clinical laboratory scientists to apply. We offer a sign-on bonus to eligible candidates. In this role, you will be responsible for preparing specimens for analysis and performing and reporting clinical laboratory procedures, ranging from waived to high complexity, all while adhering to strict compliance with written SOPs and various regulatory guidelines, including FACT, AABB, ACHI, CAP, FDA, and Joint Commission regulations. Additionally, you'll have the opportunity to assist in teaching students and staff, working under the authority of the Laboratory Director as per the Clinical Laboratory Improvement Amendments of 1988, CFR Section 493. 1445(a). Join our dynamic team at City of Hope and contribute to groundbreaking medical research and patient care. Apply now!As a successful candidate, you will: Maintain knowledge of techniques for preparing and processing biological specimens for clinical analyses using universal precautions. Demonstrate proficiency in manual, semi-automated, and automated laboratory procedures. Perform a variety of complex laboratory tests and procedures according to prescribed protocols and assigned schedules, completing them within established turnaround times. Review normal and critical results for accuracy and completeness before reporting, promptly notifying supervisors of unusual results or discrepancies. Conduct quality control procedures, including preventive maintenance, calibrations, and data recording, to support and participate in Quality Assurance efforts and the Performance Improvement process. Utilize standard laboratory equipment, ensuring accuracy and completeness of recorded results, while also performing data entry of diagnostic information. Prepare and label solutions, reagents, culture media, and stains following standard formulas and procedures. Prioritize work, provide efficient service, assist coworkers as needed, maintain cleanliness and safety practices, and uphold a high level of integrity and confidentiality while maintaining a positive customer service image when interacting with colleagues, patients, physicians, and vendors. Qualifications Your qualifications should include: Bachelor's DegreeCalifornia Clinical Laboratory Scientist (CLS) licensure City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location. City of Hope is an equal opportunity employer. To learn more about our Comprehensive Benefits, please CLICK HERE. Primary Location: United States-California-DuarteJob: Clinical Laboratory/PathologyWork Force Type: OnsiteShift: DaysJob Posting: Dec 5, 2025Minimum Hourly Rate ($): 43. 176100Maximum Hourly Rate ($): 66. 922400

Performs Laboratory testing on patient and control samples. Maintains a working knowledge of departmental standard operating procedures. This knowledge includes the use of specialized analytical instrumentation, clinical correlation of test results, quality control requirements, and preventative maintenance. Participates in the continuous quality improvement process through professional development, continuing education, data collection and evaluation and quality assurance. This position requires the full understanding and active participation in fulfilling the mission of AHMC Anaheim Regional Medical Center. It is expected that the employee demonstrate behavior consistent with the core values of AHMC- ARMC. The employee shall support AHMC Anaheim Regional Medical Center's strategic plan and goals and direction of the performance improvement plan. The employee will also be expected to support all organizational expectations including, but not limited to; Customer Service, Patient's Rights, Confidentiality of Information, Environment of Care and AHMC-ARMC initiatives. Microbilogy focus. Qualifications Education/Training/Experience Earned a doctoral or bachelor's degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution. Two years experience as a Clinical Laboratory Scientist in an acute care laboratory preferred. LICENSES/CERTIFICATIONS Current State of California Clinical Laboratory Scientist License American College of Clinical Pathologist (ASCP) registration preferred

Job Details HEMET - Hemet, CA Per Diem $50.00 - $55.00 Hourly SwingDescription The (Clinical Laboratory Scientist) CLS II plays a crucial role in our healthcare organization, contributing to accurate patient diagnoses and treatment decisions. The CLS II is responsible for coordinating and supervising activities of laboratory staff engaged in performing routine and non-routine duties. This position will also be delegated as general supervisor and must perform all duties as delegated by the laboratory director. Demonstrates sound decision-making skills involving complex laboratory tests and interpretation. Maintains the laboratory and procedures according to all State, Federal and accreditation agencies regulatory guidelines. Participates in the validation of new instruments, tests, procedures, and system software. Oversee and executes quality control and calibrates instrumentation and produces clinically accurate patient results. This is a per diem (as-needed) on call position for Hemet, CA. Hours will vary from 5:00 AM to 9:00 PM. Duties & Responsibilities: Be a proactive leader and identify opportunities and propose improvements, efficiencies, and operational modification as it relates to the laboratory operations. Will performing a wide range of complex laboratory tests, procedures, and analyses with a high degree of accuracy. Operate, maintain, and troubleshoot laboratory equipment and instruments. Ensure compliance with quality control and quality assurance protocols. Maintain accurate records of test results and patient information. Participate in the development and implementation of new laboratory procedures. Stay current with advancements in laboratory science and technology. Ensures, implement, and supports compliance with all departmental and company policies and procedures including but not limited to Quality and Safety Maintains adequate staffing and performs scheduling, planning, and monitoring of workflow based on patient load to meet established goals Resolve and troubleshoot all technical problems with the aid of the technical staff and ensures that remedial action is taken whenever a test deviates from the laboratory's performance standards Ensure that all patient results are not reported until corrective actions have been taken and the systems are functioning properly Engage in sample preparation and running clinical and other diagnostics equipment in a high complexity clinical laboratory environment. Ensure that all documentation provided associated with test results, maintenance records, and quality control are detailed, accurate and legible Ensure that instruments are running at their optimum performance through routine and preventive maintenance. Monitors performance of equipment by implementing QA and QC procedures. Monitors trends in service requests and implement corrective actions to improve operational efficiency and reduce downtime of the instruments. Supervise the lab team, including mentoring, coaching, training, developing, and building teams. Identify training needs and ensures all training is performed as required Perform staff competency assessments and annual staff performance reviews. Compose, review, update and revise new and current SOPs. Review assay QC steps and troubleshoot QC issues. Review monthly and annual instrument maintenance logs. Assist with internal and external proficiency testing. Perform instrument performance/calibration verification, as needed. Assist with the development, optimization, and validation of new assays Procures appropriate supplies and equipment to maximize efficiency within established budgetary and quality goals. Complete other tasks as needed to support the objectives of the laboratory. Qualifications Educational Requirement: o Must possess a valid CA Clinical Laboratory Scientist licensure to perform high complexity tests or must be a California-licensed physician and surgeon, and o Bachelor's degree in clinical laboratory science, medical technology or chemical, physical, or biological science with at least 1 year in high-complexity testing in the specialty or specialties of tests they will be performing; OR Other Qualification & Requirements: Familiarity with CLIA and CAP regulatory requirements. Conduct activities in compliance with CLIA and other regulatory guidelines. Adheres to laboratory safety practices, including but not limited to OSHA blood-borne pathogens, HIPAA, and hazardous chemicals training and monitoring. Identify and report unsafe equipment, conditions, and practices so that they may be corrected prior to an incident. Understanding of techniques, instrumentation, and underlying principles. Basic laboratory skills including preparing specimens and reagents. Ability to respond to common inquires or complaints from customers, regulatory agencies, or members of the business community. Ability to define problems, collect data, establish facts and of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Ability to effectively present information to top management, and /or board of directors Strong PC skills and working knowledge of MS Office. Good personal and communication skills. Self-motivated, well-organized, reliable, and able to prioritize workload.