7,722 Labcorp jobs in the United States

Job Description:

Joining The American Red Cross is like nothing else - it's as much something you feel as something you do. You become a vital part of the world's largest humanitarian network. Joining a team of welcoming individuals who are exceptional, yet unassuming. Diverse, yet uncompromising in unity. You grow your career within a movement that matters, where success is measured in people helped, communities made whole, and individuals equipped to never stop changing lives and situations for the better.

When you choose to be a force for good, you'll have mentors who empower your growth along a purposeful career path. You align your life's work with an ongoing mission that's bigger than all of us. As you care for others, you're cared for with competitive compensation and benefits. You join a community that respects who you are away from work as much as what you do while at work.

Where Your Career is a Force for Good!

WHAT YOU NEED TO KNOW:

As an IRL Technologist at the Red Cross you will perform basic and advanced donor and patient tests, and interpret results to determine donor-recipient compatibility. You will resolve compatibility problems; provide intermediate reference and consultation services to hospitals and transfusion services.

WHERE YOUR CAREER IS A FORCE GOOD

Key Responsibilities:

• Consult and communicate with staff at other medical facilities, to resolve complex serologic problems and provide special units to transfusion recipients.
• Manage receipt, coordination, shipment and transport of patient and donor blood samples. Assist in daily workflow of patient and donor work. Document supply and equipment problems.
• Manage reagent inventory including ordering, receiving, inspecting and preparing reagents. Perform and interpret basic and complex donor and/or patient testing procedures and complete required quality control, as appropriate to state and federal regulations.
• Recognize testing irregularities, identify the cause, determine the solution and resolve the problem. Assist Technologist I and II in problem resolution. Maintain, edit and review computer and manual records to assure accurate record keeping. Maintain accurate, legible and complete records.
• Also perform maintenance, repair and validation of laboratory equipment and software maintenance. Assume lead responsibilities such as record review and training. Assist in concern management.

Standard Schedule : The position requires a Monday to Friday work week, with varying schedules from either 7:00 AM to 3:30 PM or 8:00 AM to 4:30 PM. In addition, this position includes on-call responsibilities for weekends and holidays. On-call shifts are assigned weekly, beginning after regular business hours on Friday (post 4:30 PM) and continuing until the following Friday morning (up to 6:59 AM).

Pay: The salary range for this position is (California): $55/hr

Note that American Red Cross salaries are aligned to the specific geographic location in which the work is primarily performed. Other factors that may be used to determine your actual salary may include your specific skills, how many years of experience you have and comparison to other employees already in this role.

WHAT YOU NEED TO SUCCEED:

• Bachelor's degree in Biological Science or Chemistry with MLS ( ASCP ) or BB(ASCP) or equivalent certification required.
• Licensure if required by state.
• Good written and verbal skills to communicate effectively with internal and external customers. Leadership skills. Ability to work on a team.

WHAT WILL GIVE YOU THE COMPETITIVE EDGE:

• SBB (ASCP) preferred
• Minimum 4 years of related experience or equivalent combination of education and related experience preferred.

Physical Requirements: Requires standing, stretching, stooping and bending for extended time periods. Lift, pull, push and move objects of up to 50 pounds. May work in walk-in refrigerator/freezers for periods of time. Required to wear protective clothing such as lab coats, gloves, face shields, etc. Ability to use a wide variety of lab or medical equipment.

BENEFITS FOR YOU: As a mission-based organization, we believe our team needs great support to do great work. Our comprehensive package includes:

• Medical, Dental Vision plans
• Health Spending Accounts & Flexible Spending Accounts
• PTO: Starting at 15 days a year; based on type of job and tenure
• Holidays: 11 paid holidays comprised of six core holidays and five floating holidays
• 401K with up to 6% match
• Paid Family Leave
• Employee Assistance
• Disability and Insurance: Short + Long Term
• Service Awards and recognition

The American Red Cross is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.

Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers, San Diego Fair Chance Ordinance, the California Fair Chance Act and any other applicable state and local laws.

AmeriCorps, the federal agency that brings people together through service, and its partners - the Peace Corps, AmeriCorps Alums, National Peace Corps Association, and the Service Year Alliance - launched Employers of National Service to connect national service alumni with opportunities in the workforce.American Red Cross is proud to be an EONS partner and share our employment opportunities with the network of organizations.

Interested in Volunteering? Visit redcross.org/volunteertoday to learn more, including our most-needed volunteer positions.

To view the EEOC Summary of Rights, click here: Summary of Rights

• Be on the Cutting Edge! Work with the latest technology and a top-notch interdisciplinary team to help support patients and the community. As a Clinical Laboratory Scientist, you will perform a variety of complex testing with the goal of detecting, diagnosing, and treating disease. The work you will be doing makes a tremendous impact!
  
  
• Develop and Grow your Career! Invest in furthering your education through seeking certifications or advanced degrees by taking advantage of our Tuition Reimbursement! This position is eligible for up to $,000 per year based upon your full or part Time status.
  
  
• Benefits: Annually, you are eligible for up to four (4) weeks of paid time off. We offer a number of employee discounts to various activities, services, and vendors including free employee parking
  
  

Required Experience

• Must have skills necessary to perform procedures contained in the laboratory procedure manual, including specimen processing, test performance and reporting test results.
• Demonstrated communication, organization, and prioritization skills required.
• Previous laboratory computer system experience preferred.
  

Required Education & Licensures/Certifications:

• Bachelor's degree in an accredited Medical Laboratory Technician program or related field
• Equivalent combination of education and experience required.
• MLT (ASCP) or equivalent certification preferred

• Requisition ID: 2500081
• Employee Status: Regular
• Benefit Eligibility: Full-Time Benefits
• Schedule: Full-time
• Pay Range: 29.60 - 45.86
• Job Grade: 210

Surgery

Full Time

85381BR

Job Summary

Perform laboratory functions that support solid organ and blood & marrow transplant programs. Functions include on-call responsibilities for the deceased donor transplant programs; perform infectious disease testing; data entry of patient and sample information into various systems, prepare cell subsets; isolate DNA; HLA type by various methods; crossmatch by flow cytometry method; test and identify HLA antibodies; chimerism monitoring and other HLA-related tests; assist in managing samples (store, retrieve, and aliquot samples); perform quality control and routine maintenance of various laboratory equipment; analyze and report laboratory data; order supplies, repairs, and other services; answer phones and perform other duties as assigned.

The final salary and offer components are subject to additional approvals based on UC policy.

Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.

The salary range for this position is $63.62 - $79.25 (Hourly Rate).

To learn more about the benefits of working at UCSF, including total compensation, please visit:

Department Description

The mission of the UCSF Department of Surgery is threefold: to develop the next generation of leaders in surgery; to provide outstanding quality clinical care that is cost effective, yet compassionate; and to make significant advances in scientific knowledge and clinical practice through basic and clinical research. Care of patients is what attracted our faculty and residents to surgery, and it continues to be our main focus. The Department is comprised of seven divisions including Adult Cardiothoracic Surgery, General Surgery, Pediatric Cardiothoracic Surgery, Pediatric Surgery, Plastic & Reconstructive Surgery, Transplant Surgery, and Vascular & Endovascular Surgery.

The UCSF-ITL is a high complexity clinical laboratory that performs tests and provides services that support solid organ (kidney, heart, lung, liver, pancreas, islet, etc.) and hematopoietic stem cell (blood, marrow, cord blood, etc.) transplant programs. The laboratory is CLIA certified and is licensed by the states of California and New York. The lab is also certified as a free-standing-histocompatibility laboratory by the Centers of Medicare and Medicaid (CMS). The laboratory serves as a core laboratory for the NIH Immune Tolerance Network and provides support for several national clinical trials.

Required Qualifications

• Graduation from college with a major in an appropriate scientific field, possession of a clinical laboratory Scientist's license or a similar license of equal or higher level issued by the California Department of Health; and knowledge and abilities essential to the successful performance of duties assigned to the position.
• Current California Clinical Laboratory Scientist (CLS) Generalist or Clinical Histocompatibility Scientist license.
• Relevant laboratory experience and/or a degree in life science or related course.
• Must be able to perform on-call duties including reporting to the laboratory within an hour of notice or call.
• Must be able to work variable shifts as required by laboratory operations including weekends, nights, and early mornings.
• Accurate and be able to process multiple samples without switches.
• Be able to work with personal computers.
• Must be effective as a member of a team.
• Proven record of being reliable and be able to multi-task.
• Must be able to work independently with minimum supervision.
• Proficient in communication and interpersonal skills to communicate effectively, both verbally and in writing.
• Tidy and orderly.

Preferred Qualifications

• Advance degree (Masters or doctorate) in a relevant field (e.g., immunology, blood banking, and biochemistry).
• Experience with QC/QA/QS in a clinical laboratory setting.
• Working knowledge of antigens and genetics of the HLA system and be able to interpret results correctly.

License/Certification

• Current California Clinical Laboratory Scientist (CLS) Generalist or Clinical Histocompatibility Scientist license.

About UCSF

The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world's leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.

Pride Values

UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence - also known as our PRIDE values.

In addition to our PRIDE values, UCSF is committed to equity - both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available at diversity.ucsf.edu

Join us to find a rewarding career contributing to improving healthcare worldwide.

Equal Employment Opportunity

The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.

Organization

Campus

Job Code and Payroll Title

008940 CLIN LAB SCI

Job Category

Clinical Labs

Bargaining Unit

University Professional and Technical Employees - Health Care Professionals Unit (UPTE-HX)

Employee Class

Career

Percentage

100%

Location

San Francisco, CA

Campus

Downtown (SF)

Work Style

Fully On-Site

Shift

Variable

Shift Length

Variable

Additional Shift Details

Variable depending upon the needs of the lab

Description:
Could you be our next Clinical Lab Scientist at Lankenau Hospital? This position is eligible for a 5k Sign On Bonus!

Why work as a Clinical Lab Scientist with Main Line Health?

• Be on the Cutting Edge! Work with the latest technology and a top-notch interdisciplinary team to help support patients and the community. As a Clinical Laboratory Scientist, you will perform a variety of complex testing with the goal of detecting, diagnosing, and treating disease. The work you will be doing makes a tremendous impact!
  
  
• Develop and Grow your Career! Invest in furthering your education through seeking certifications or advanced degrees by taking advantage of our Tuition Reimbursement! This position is eligible for up to $6,000 per year based upon your Full or Part Time status.
  
  
• Join the Team! Like our patients, the Main Line Health Family encompasses a wide range of backgrounds and abilities. Just as each of our patients requires a personalized care plan, each of our employees, physicians, and volunteers, bring distinctive talents to Main Line Health. Regardless of our unique design, we all share a purpose: providing superior service and care.
  
  
• Position-Specific Benefits include: You are eligible for up to 160 hours of paid time off per year based on your Full or Part Time status. We also offer a number of employee discounts to various activities, services, and vendors. And employee parking is always free!
  
  

Position: Clinical Laboratory Scientist in Stat Lab
Shift: Monday-Friday 11:00pm-7:30am. Weekends and Holidays based on department needs

Experience:
1. Must have skills necessary to perform procedures contained in the laboratory procedure manual, including specimen processing, test performance and reporting test results.
2. Demonstrated communication, organization, and prioritization skills required.
3. Previous laboratory computer system experience preferred.

Education:
1. Bachelor's degree in an accredited Medical Laboratory Technician program or related field
2. Equivalent combination of education and experience required.

Licensures/Certifications:
MLT (ASCP) or equivalent certification preferred.

• Requisition ID: 70618
• Employee Status: Regular
• Benefit Eligibility: Full-Time Benefits
• Schedule: Full-time
• Shift: Night Job
• Pay Range: $9.6 - 45.86
• Job Grade: 210

Description

Methodist Stone Oak Hospital

Clinical Laboratory Scientist I

Laboratory Department

PRN - Non-Exempt

Do you have a passion for healthcare and helping others? Do you enjoy working in a fast-paced, patient-centered environment? Jump-start your career in our Laboratory Department. Submit your application today!

Benefits:

We offer you an excellent total compensation package, including competitive salary, excellent benefit package and growth opportunities. We believe in our team and your ability to do excellent work with us. Your benefits include 401k, PTO medical, dental, flex spending, life, disability, tuition reimbursement, employee discount program, employee stock purchase program, and student loan repayment. We would love to talk to you about this fantastic opportunity.

Clinical Laboratory Scientist I is responsible for performing routine and complex medical laboratory tests and analysis of results; assuming accountability for accurate results and responsibility for assigned equipment within section/department.

What you will do In This Role:

• Performs specimen processing and testing independently to include moderate and high complexity testing.
• Analyzes test results - demonstrates knowledge of pathological processes with correlation of disease states and test results.
• Understands, performs, and practices preventive maintenance on assigned equipment; troubleshoots and takes corrective action.
• Understands, performs, and practices quality control to include running controls, evaluating data, documentation of data, and taking corrective action as required. Communicates any relevant QC information to supervisor/lead tech.
• Assumes responsibility for own development; meets timeliness for gaining skills. Satisfactorily completes competency checklist for this position
• Provides technical information about test results to physicians, nurses and patients. Acts as a resource to others.

• A. High school diploma (or equivalent), with 4 years of clinical lab experience. or
• B. Associates Degree from an accredited MLT training program. -OR
• D. Bachelors Degree from a 4 year accredited CLS program.

Minimum License and Certificates Required: Not Applicable

Methodist Hospital Stone Oak continues to grow and build on our reputation as a hospital where high-tech and high-touch come together. It is a streamlined, energy-efficient, patient-focused health care facility equipped with the most modern technology available. With over 280 beds, services include emergency care, general surgery, obstetrics and gynecology, neonatology, oncology, neurosurgery, orthopedics, and acute rehab services.

Methodist Hospital Stone Oak is accredited by the Joint Commission as a Primary Stroke Center and Chest Pain Center. The stroke rehabilitation program has received the Joint Commission's Gold Seal of Approval for Disease-Specific Care Certification of Stroke Rehabilitation. Methodist Hospital Stone Oak belongs to the Texas Institute for Robotic Surgery and has become a leader in robotic surgeries with a highly experienced team of surgeons offering this minimally invasive option to patients. Surgeons from around the country come to train under the facilitys world class team. The hospital has been nationally recognized by Leapfrogs Hospital Safety Grade A and by Modern Healthcare as one of the Top 100 Best Places to Work in Healthcare. It also been recognized as a Joint Commission Top Performer on Key Quality Measures and by Medicare.gov as #1 in San Antonio and #6 in the entire nation. Methodist Hospital Stone Oak is 1 of only 102 hospitals to receive Medicare.govs 5-star rating. For more information, please visit our website at and select Methodist Hospital Stone Oak under Locations.

Be a part of an organization that invests in you. We are actively reviewing applications. Qualified candidates will be promptly contacted by our hiring managers for interviews. Submit your application today and help us raise the bar in patient care!

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability.

Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, Labcorp wants to speak with you about exciting opportunities to join our team as a Technologist in Daphne, AL. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at Labcorp: “Improving Health, Improving Lives”.

Work Schedule: 1st Shift, Monday - Friday 7:00AM - 3:30PM

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.  Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. 

Job Responsibilities

• Determine the acceptability of specimens for testing according to established criteria
• Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures
• Monitor, operate and troubleshoot instrumentation to ensure proper functionality
• Demonstrate the ability to make technical decisions regarding testing and problem solving
• Prepare, test and evaluate new reagents or controls
• Report accurate and timely test results in order to deliver quality patient care
• Perform and document preventative maintenance and quality control procedures
• Identify and replenish testing bench supplies as necessary
• Assist with processing of specimens when needed
• Maintain a safe work environment and wear appropriate personal protective equipment

 Requirements

• Bachelor’s degree in Chemical or Biological science, Clinical Laboratory Science, Medical Technology or a non-traditional Bachelor’s degree that meets local regulatory (CLIA & State) requirements
• Minimum 1 year of clinical laboratory testing experience is required OR a MLS degree
• ASCP or AMT certification is preferred
• Ability to work independently and within a team environment
• Proficient with computers; Familiarity with laboratory information systems is a plus
• High level of attention to detail along with strong communication and organizational skills
• Must be able to pass a standardized color vision screen
• Flexibility to work overtime or other shifts depending on business needs

Y ou're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. 

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit ouraccessibility siteor contact us atLabcorp Accessibility. Formore information about how we collect and store your personal data, please see ourPrivacy Statement.

Execute Clinical and analytical testing in the US to support product development for new Hematology and Hemostasis products(reagents and analyzers). Works with R&D, Clinical and Regulatory in the US and France to verify and validate that new products meet pre-defined specifications and requirements, the intended use, user needs, and requirements in the real-world operational environment as well as U.S. regulatory requirements. Provides comprehensive knowledge of instrument operation in support of clinical validation. Delivers a comprehensive overview of various lab and clinical trials and research projects as needed.Essential Duties & ResponsibilitiesStays current with product and instrument capabilities in order to advise the organization regarding important scientific developments as well as creating and maintaining a scientific and technical relationship with opinion leaders.Maintain awareness of new and updated testing standards in order to provide support to clinical trial designs and execution.Interacts with groups, such as but not limited to CLSI, CLIA and CAP in order to ensure Stago is at the forefront of the market's evolutionWorks closely with the NCRA to help support validation trials in the US in support of new Hematology and Hemostasis products and parts.Works closely with French counterparts to help conduct and support verification activities as well as clinical validation activities in the US in facilitation of new Hematology and Hemostasis product launches.Verify technical conditions prior to the start of a study, ensure instruments are in pristine working order and maintenanceof equipment is up to date to ensure successful study conditions.Ensures full understanding of the protocol requirements to ensure the study proceeds efficiently in order to meet organizationaltime lines.Participates in the development of study related materials needed to execute verification and validation studies and may periodically be required to lead these effortsAssist with the execution of clinical and analytical studies to support new and existing products and reports results to all external stakeholders (biologists, clinicians, lab techs)Ensures a field presence during validation study activities and may be a point of contact for the external sites participating in the studies.Verify the technical conditions of study staff prior to the start of study, conduct necessary training of personnel and ensure maintenance of equipment is up to date for successful study conditions.Ensure corrective actions are followed for proper conduct to freeze databases of results in accordance with the studies initial objectives.Check completeness of records (all forms of media: paper and electronic), ensures centralization and formatting of data from studies, as well as ensuring traceability of dataUses knowledge and experience with instrument validation to perform interference, on-board stability, real-time-stability, Limit of Blank, Limit of Detection, Limit of quantification, Linearity, precision and Method Comparison testing.Utilizing local members of the service operations, create good logistical conditions for verification and validation studies to include but are not limited to delivery of reagents and/or instrument, exchange of correspondence, contracts and administrative documents.Ensures successful protocol implementation and monitors analytical protocol execution to ensure the quality of the study data as well as the study proceeding efficiently in order to meet organizational timelines.Documents all necessary follow-up to study in accordance with defined procedure including but not limited to monitoring plan, checklist of setting up visits, monitoring, etc.Enters data into databases, online systems, or other means depending on the study designs, as neededIssues queries to resolve errors and missing dataCollects agreements, records, labels, forms, study reports or other study documentation as applicable.Maintain laboratory equipment following daily, weekly and monthly maintenance schedules as well as required quality control for all laboratory analyzers.Participates in validation of new equipment as appropriateAssists the NCRA's in the development and maintenance of clinical study binders and utilization of eCRF.Manages the Laboratory equipment service contracts and documentary elements of verification and validation studies.Completes the necessary documentation and reports for verification/validation studies performed in the laboratory.Completes necessary clinical trial documentation from the site's perspective, in preparation of study start up, if required.Give scientific presentations as required.Offer support on new product launches as needed.QualificationsB.S. Medical Technology/Clinical Laboratory Science or equivalent from an accredited four-year college or university required; MT(ASCP) Certification or equivalent preferred; Minimum of two years experience as a Technical Support Specialist or Field Support Engineer with Hematology and Coagulation instrumentation required, external or Stago experience, or minimum five years hospital experience in Hematology and Coagulation preferably experienced with validations, correlations and training lab staff on new laboratory instrumentation.Experience designing, organizing, and conducting clinical trials is a plus.Demonstrated competency in the review of statistical analysis methods for clinical data is a plus.Experience in IVD product development is a plus.To perform this job successfully, an individual should be familiar with Excel and Windows Office Suite Applications and other company software.ASCP preferred.Ability to read, analyze and interpret complex documents; respond effectively to technical inquiries and customer complaints. Ability to write and deliver effective and persuasive technical and non-technical presentations to senior management, sales and service staffs, and customer representatives. Ability to work with mathematical concepts such as probability and statistical inference. Up to 50% U.S. travel required during execution of studies. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.We offer an extensive benefit and compensation package that includes medical, dental, vision, FSA, 401k, PTO, life and disability insurance, as well as a comprehensive leave program. Pay anticipated for this position in New Jersey is from $68,000-88,000, depending on a number of factors. This role is also anticipated to be eligible to participate in a bonus plan and an automobile plan which are associated with this position. In the ordinary course of business, compensation and benefits programs may change based upon the Company's needs.All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, disability or protected veteran status. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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 Laboratory, Clinical, Scientist, Healthcare, Quality Control, Specimen

• Perform a broad range of laboratory procedures, including all testing and tasks of the medical laboratory technologist occupation.
• Conducted complex analyses of patient samples, including blood, urine, body fluids, and other specimens, to detect and identify diseases.
• Interpret and report laboratory results, ensuring accurate, timely data is available for informed patient care decisions.
• Follow quality control, quality assurance, safety, and infection control procedures.
• Maintain up-to-date knowledge of instrumentation and test methodologies.
• Collaborate with healthcare teams to determine the best course of action for patient care.
• Participate in the evaluation of new techniques and procedures in the laboratory.
• Train and supervise other laboratory personnel as necessary.
• Maintain all laboratory records in compliance with hospital policies and regulatory requirements.

• A bachelor's degree in medical technology or a related Science field.
• Current and valid Clinical Laboratory Scientist license from California state.
• Minimum of 1-3 years of experience in a hospital laboratory setting.
• Experience with automated and manual testing procedures.
• Excellent analytical and problem-solving skills.
• Strong communication skills, both written and verbal.
• Attention to detail and ability to work under pressure.