Laboratory assistant jobs in Kentucky

Shift: 1:00 AM to 9:30 AM; Tuesday-Saturday Training: 2-weeks from 1:00 AM to 9:30 AM; Monday-Friday Who is HealthTrackRx? HealthTrackRx is the nation's leading PCR-based infectious disease laboratory! By delivering next morning results to healthcare providers nationwide, HealthTrackRx is the premier option for patients and healthcare professionals and in an exciting phase of growth! Job Summary: Lab Assistant is responsible for accessing patient sample information into the Laboratory Information Management System (LIMS), accurately according to received requisitions. Able to assist in troubleshooting issues with patient samples and effectively communicate internally and externally. Essential Responsibilities/Duties: * Review all information to be accurate and meet the company's and regulatory standards * Accepts deliveries from couriers * Accession patient sample information and physician test orders according to requisitions, accurately * Provide oversight of orders on requisitions on pre-accessioned samples * Identify missing information and execute proper route when missing information is identified * Scan patient requisitions for medical records * Maintain a reportable error rate below .05% with a goal of zero errors per month * Verify required information, per HIPPA/CAP/CLIA, is obtained on all orders * Responsible for adherence to annual safety, compliance and HIPPA training Qualifications: Education - * High School diploma or equivalent * Competencies/Skills - * Strong organizational skills * Ability to maintain confidentiality of all medical, financial, and legal information * Ability to work independently * Effective oral communication skills Experience - * 6 months experience working in a laboratory environment, preferred * Experience working with MS Office required Let's talk about benefits * Health, dental and vision * 401(k) match * Health Savings Account (HSA) * Flexible Spending Account (FSA) * Tuition Reimbursement * Plus much more

between Brannon Crossing, Andover and Veterans Park. The Certified Medical Assistant/Lab Assistant functions as a member of the patient care team, contributing to the health management of the patients; performs a variety of patient care activities and accommodative services for Clinic patients, many in assistance to section physicians and under the direction and supervision of the Patient Care Manager; maintains primary responsibility for all technical procedures and the operation and care of the nursing unit in the department.. Under the direction of the Laboratory Director, enhances and extends the productivity of Clinical Laboratory Scientists by performing patient accommodative services including phlebotomy, specimen receipt, specimen processing and technical procedures as assigned; assumes other duties and responsibilities as directed by Supervisor. PREFERRED QUALIFICATIONS: Formal training which will probably be indicated by certification from an accredited medical assistant program; current CPR certification required; two years broad experience with emphasis in family practice. Prefer additional experience as a laboratory assistant/phlebotomist. PHYSICAL GUIDELINES: Physical guidelines include the ability to move, traverse, position self, remain in a stationary position and negotiate steps for up to eight hours per day; lift, move and transport patients, maneuver objects, equipment, and supplies weighing up to 20 pounds; visual and auditory acuity; distinguish colors; motor coordination and manual dexterity; articulate speech; ability to read and understand orders, exposure to hazardous/bio-hazardous materials. NOTE: This document is intended to describe the general nature and level of work performed. It is not intended to act as an exhaustive list of all duties, skills, and responsibilities required of personnel so classified. Attendance is an essential function of the job. LEXINGTON CLINIC IS AN EQUAL OPPORTUNITY EMPLOYER (EOE)

Shift: 1:00 AM to 9:30 AM; Tuesday-Saturday Training: 2-weeks from 1:00 AM to 9:30 AM; Monday-Friday Who is HealthTrackRx? HealthTrackRx is the nation's leading PCR-based infectious disease laboratory! By delivering next morning results to healthcare providers nationwide, HealthTrackRx is the premier option for patients and healthcare professionals and in an exciting phase of growth! Job Summary: Lab Assistant is responsible for accessing patient sample information into the Laboratory Information Management System (LIMS), accurately according to received requisitions. Able to assist in troubleshooting issues with patient samples and effectively communicate internally and externally. Essential Responsibilities/Duties: Review all information to be accurate and meet the company's and regulatory standards Accepts deliveries from couriers Accession patient sample information and physician test orders according to requisitions, accurately Provide oversight of orders on requisitions on pre-accessioned samples Identify missing information and execute proper route when missing information is identified Scan patient requisitions for medical records Maintain a reportable error rate below .05% with a goal of zero errors per month Verify required information, per HIPPA/CAP/CLIA, is obtained on all orders Responsible for adherence to annual safety, compliance and HIPPA training Qualifications: Education - High School diploma or equivalent Competencies/Skills - Strong organizational skills Ability to maintain confidentiality of all medical, financial, and legal information Ability to work independently Effective oral communication skills Experience - 6 months experience working in a laboratory environment, preferred Experience working with MS Office required Let's talk about benefits Health, dental and vision 401(k) match Health Savings Account (HSA) Flexible Spending Account (FSA) Tuition Reimbursement Plus much more

Job Description Under the supervision of the MCCH Laboratory technical staff, performs specimen collection and processing, clerical tasks, point of care testing, and other laboratory support staff duties as assigned. The position reports to the Laboratory Director through the MCCH Laboratory technical staff. The Lab Assistant also maintains cooperative working relationships with intradepartmental and interdepartmental personnel. Minimum Work Experience: Phlebotomy experience required Minimum Education: High School diploma required, college courses in biology and science preferred Eligible Benefits: Medical, Dental and Vision *Excellent Low Premiums!*- No copays or Deductibles when utilizing MCCH services! Life Insurance *ZERO premium* Retirement Plan Paid Time Off Bereavement Tuition Reimbursement Screening Requirements: Drug Screen Tuberculosis Test Background Check Physical Exam Respirator Fit Our Mission: To improve the lives of those we serve by providing outstanding care and services through our confident, compassionate and exceptional healthcare professionals Our Vision: To be chosen by our community and expanded service region based on proven outcomes as the trusted provider to care for their families, friends and neighbors Our Values: Compassion, Competence, Excellence, Respect, Integrity

Shift: 2am-1030am Lab Accessioner 1 The Laboratory Accessioner helps prepare samples and supports lab operations as requested. The Accessioner is responsible for receiving, labeling, and preparing specimens for laboratory testing while ensuring adherence to standard operating procedures, safety protocols, and quality control guidelines. Job Duties: Accountable for understanding and following the laboratory's standard operating protocols, quality control processes, and safety rules. Receives and accessions specimens into the Laboratory Information Management System. Unpacks specimens and routes specimens by type to various staging areas. Prepares all specimens received for testing in designated laboratory departments or locations such as staging of specimens, centrifuge, etc. Prepares excess specimen samples for storage and resolves and documents problem specimens. Organizes work by matching computer orders with specimen labeling, sorting specimens, checking labeling, logging specimens and arranging reports for delivery. Accountable for keeping work surfaces clean and orderly. Participates in all applicable safety training sessions to ensure thorough understanding and execution of safety procedures, including the use of all applicable safety equipment. Organizes and maintains lab specimen storage. Organizes and monitors lab supplies for appropriate inventory levels. ·Perform other duties as directed by supervisor. Education/Experience: · HS Diploma or GED equivalent required · 1-2 years of experience in data entry preferred · Medical background or experience with laboratory testing terminology or a strong aptitude to learn terminology preferred Technical Skills Required: · Proficiency in Microsoft Platforms (Teams, Outlook, Word etc.) · Detail oriented, flexible, quick to learn · Proficient in data entry · Organizational abilities · Able to work productively, effectively, and independently in a fast-paced environment · Ability to handle multiple tasks systems · Effective verbal and written communications, especially listening skills · Detailed orientated with regards to data entry and excellent typing skills · Strong computer skills and ability to work within windows environment · Must be comfortable in a fast-paced environment with target productivity rates Physical Position Requirements: · Ability to lift up to 50 pounds · Ability to bend, kneel, stoop, crouch · Ability to walk, sit, or stand for extended periods · Ability to use tools such as boxcutters · Ability to wear PPE for extended periods of time Full time RegularColleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Laboratory Coordinator, Acute Jackson Purchase Medical Center Full Time | Days Who We Are: People are our passion and purpose. Come work where you are appreciated for who you are not just what you can do. Jackson Purchase Medical Center is a 107 all private bed, Joint Commission-accredited facility. From emergent to elective, our facility offers a wide variety of inpatient and outpatient services, including those offered at the New Beginnings Birthing Center, the Advanced Healing Wound Care Center and our accredited chest pain center. Where We Are: Mayfield is located in stunning western Kentucky, just a short drive to Kentucky Lake to the east, the Ohio River to the north, and the Mississippi River to the west. Here you find there is always something for all ages, whether it's outdoor sports and recreation, visual and dramatic arts, or even living history. Connect with our recruiting specialist Not ready to complete an application, or have questions? Please contact Melissa Gilbert by texting ************, calling ************ or schedule a time and date that works for you by clicking the link below. *********************** Why Choose Us: We believe that investing in our employees is the first step to providing excellent patient care. In addition to your base compensation, this position also offers: Comprehensive Benefits: Multiple levels of medical, dental and vision coverage for full-time and part-time employees. Financial Protection & PTO: Life, accident, critical illness, hospital indemnity insurance, short- and long-term disability, paid family leave and paid time off. Financial & Career Growth: Higher education and certification tuition assistance, loan assistance and 401(k) retirement package and company match. Employee Well-being: Mental, physical, and financial wellness programs (free gym memberships, virtual care appointments, mental health services and discount programs). Professional Development: Ongoing learning and career advancement opportunities. Position Summary: The Laboratory Coordinator shall perform and demonstrate proficiency and understanding in one or more areas of the clinical laboratory, assistance in instructing other personnel as assigned, performs with a perceptive depth of clinical laboratory tests and procedures which require the exercise of independent judgments and responsibility. Maintains the highest degree of quality patient care at all times. This position is also responsible for LIS. This includes but is not limited to system file maintenance and the maintenance of the ongoing laboratory quality assurance program. Performs diagnostic testing on patient samples to aid physicians in the diagnosis and/or monitoring of various disease states. Follows standardized procedures and helps prepare samples for testing. Collects samples and analyze bodily fluids and substances for abnormalities. Operates laboratory equipment in a high-quality, effective manner. Analyzes test results for accuracy, acceptability, and critical limits, and reports/documents results per organizational standards. Performs automated tests using computerized instruments & automated equipment. Performs manual tests based on detailed instructions from a physician. Runs tests and analyzes the results to be reported to the patient, physician, registered nurse or other licensed person. Performs Quality Control work to ensure accuracy of equipment and tests performed. Assist Lab Assistants as needed. Analyze samples used for transfusions. Collects specimens, including blood from patients. Completes annual competencies in a timely manner. Performs instrument maintenance and troubleshooting. Maintains Supplies. Reports critical values in a timely manner. Observes professional ethics in maintaining confidential information regarding the financial, personal, medical or employment status of patient/families. Must follow and enforce accepted safety practices for patients and hospitals. Must report safety hazards and initiate appropriate action. Must participate in safety instructional programs. Maintains compliance with CAP, State, Federal and other regulatory and accrediting agency standards related to job duties. Demonstrates professional and independent judgment at all times. Assists with Performance Improvement activities in the department and serves on teams as needed. Acts as a liaison between LIS and HIS. Trains and educates all laboratory personnel on LIS. Provides technical support in solving procedural problems. Presents appropriate in-service lectures to laboratory and other professional staff. Minimum Qualifications: Associate's in MLT or Bachelor's in MT Required Associate's or Bachelor's in Medical Laboratory Science Preferred AMLT Certification or Equivalent Required within 1 year of hire ASCP or Equivalent preferred EEOC Statement: Jackson Purchase Medical Center is committed to providing Equal Employment Opportunities for all applicants and employees and complies with all applicable laws prohibiting discrimination against any employee or applicant for employment because of color, race, sex, age, religion, national origin, disability, genetic information, gender identity, sexual orientation, veterans' status or any other basis protected by applicable federal, state or local law.

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. Job Description Since 1999, Eurofins Genomics Blue Heron(Blue Heron Biotech) has been a pioneer in the gene synthesis industry and has delivered tens of millions of base pairs of perfectly accurate genes to thousands of customers worldwide using its proprietary GeneMaker multi-technology platform. We are 100% committed to serving our customers with high quality, strict confidentiality standards, and rapid delivery of synthesized genes, Plasmid DNA, and IVTmRNA. Core Responsibility: Responsible for all activities related to plasmid preparation, including colony picking, culturing, plasmid DNA preps, DNA sequencing, bacterial transformation, media preparation, and labware cleaning. Position Responsibilities/Accountabilities but are not limited to: Work within the Plasmid team and routinely perform mini, midi, maxi, and giga preps in a high-throughput setting. Transforming, picking and culturing E.coli colonies. Prepare glycerol stocks and plasmids for sequencing and quantifying DNA by O.D. Identifying and troubleshooting issues that arise during the production process. Record all actions in the status log, including the conditions and the concentrations of targets. Prepare media and all other required reagents. Labware cleaning and autoclaving Prepare final products for shipping Work within a multi-disciplinary team, meet goals for accuracy, production deadlines and throughput utilizing the company's proprietary gene-synthesis platform. Execute production protocols in accordance with established company procedures under the ISO 13485 standard. Maintain clear communication, professionalism, and a strong work ethic. Stock laboratory with supplies in addition to cleaning and decontaminating laboratory instruments and work area daily Perform any additional duties as directed by Lab management Reporting Relationship: Reports to Gene Assembly Manager/ Production Manager Qualifications Associate or Bachelor Degree in Life Science. 1+ years lab experience related to biology, molecular biology, biochemistry, or chemistry. The ideal candidate is self-motivated, highly organized, and able to work effectively as part of a team. They should have a basic understanding of molecular biology. Familiarity with basic spreadsheet use, along with precise attention to detail, accurate record-keeping, and adherence to protocols, is required. Work experience in a high-throughput laboratory, sequencing group, or genome center is a plus. Additional Information This is a full-time position that includes weekend work based on scheduling needs. Shifts may be Sunday to Thursday or Tuesday to Saturday, from 8:00 AM to 5:00 PM or 12:00 PM to 9:00 PM. Candidates living within a commutable distance of Louisville, KY are encouraged to apply. 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 Eurofins USA Genomic Services 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. Job Description Since 1999, Eurofins Genomics Blue Heron(Blue Heron Biotech) has been a pioneer in the gene synthesis industry and has delivered tens of millions of base pairs of perfectly accurate genes to thousands of customers worldwide using its proprietary GeneMaker multi-technology platform. We are 100% committed to serving our customers with high quality, strict confidentiality standards, and rapid delivery of synthesized genes, Plasmid DNA, and IVTmRNA. Core Responsibility: Responsible for all activities related to plasmid preparation, including colony picking, culturing, plasmid DNA preps, DNA sequencing, bacterial transformation, media preparation, and labware cleaning. Position Responsibilities/Accountabilities but are not limited to: Work within the Plasmid team and routinely perform mini, midi, maxi, and giga preps in a high-throughput setting. Transforming, picking and culturing E.coli colonies. Prepare glycerol stocks and plasmids for sequencing and quantifying DNA by O.D. Identifying and troubleshooting issues that arise during the production process. Record all actions in the status log, including the conditions and the concentrations of targets. Prepare media and all other required reagents. Labware cleaning and autoclaving Prepare final products for shipping Work within a multi-disciplinary team, meet goals for accuracy, production deadlines and throughput utilizing the company's proprietary gene-synthesis platform. Execute production protocols in accordance with established company procedures under the ISO 13485 standard. Maintain clear communication, professionalism, and a strong work ethic. Stock laboratory with supplies in addition to cleaning and decontaminating laboratory instruments and work area daily Perform any additional duties as directed by Lab management Reporting Relationship: Reports to Gene Assembly Manager/ Production Manager Qualifications Associate or Bachelor Degree in Life Science. 1+ years lab experience related to biology, molecular biology, biochemistry, or chemistry. The ideal candidate is self-motivated, highly organized, and able to work effectively as part of a team. They should have a basic understanding of molecular biology. Familiarity with basic spreadsheet use, along with precise attention to detail, accurate record-keeping, and adherence to protocols, is required. Work experience in a high-throughput laboratory, sequencing group, or genome center is a plus. Additional Information This is a full-time position that includes weekend work based on scheduling needs. Shifts may be Sunday to Thursday or Tuesday to Saturday, from 8:00 AM to 5:00 PM or 12:00 PM to 9:00 PM. Candidates living within a commutable distance of Louisville, KY are encouraged to apply. 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 Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.

The role of a Lab Coordinator assists all team members of the clinical research team. The Lab Coordinator is responsible for ensuring all lab activities are completed timely, accurately, and per study protocol. This position includes but not limited to processing lab samples, shipping lab samples per protocol specification and timeline. To consistently embody AMR Clinical's Core Values: United We Achieve Celebrate Diverse Perspectives Do the Right Thing Adapt and Persevere The Lab Coordinator reports to the Site Manager/Lab Manager. Classification: Non-Exempt Primary Responsibilities: Ensure Compliance with Regulatory & Safety Standards - Adhere to Good Clinical Laboratory Practices (GCLP), ICH-GCP, FDA, IATA, and OSHA regulations when handling and processing specimens. Perform Quality Control Checks - Regularly inspect sample processing, storage conditions, and lab documentation to ensure compliance and prevent deviations. Troubleshoot Lab Processing Issues - Identify and resolve sample processing delays, equipment malfunctions, and protocol deviations to prevent disruptions. Support Sponsor & Monitor Requests - Assist with remote and on-site lab monitoring visits, including document retrieval, sample reconciliation, and audit preparation. Develop & Implement Lab Training Programs - Train new team members on lab protocols, safety measures, and compliance requirements. Collaborate with Study Teams to Optimize Workflows - Work with monitors, clinical staff, CRCs, and regulatory teams to improve lab processes and efficiency. Draw labs and collect specimen per the study protocol Process and store lab specimens per study protocol Package lab specimens according to study protocol. Ship lab specimens per study protocol Answer queries in a timely manner Inventory lab supplies Unpack and put away supplies and study materials received from study sponsors. Maintain logs for refrigerator and freezers Maintain logs for required equipment Ensure calibration is maintained on all equipment Complete forms and study documents with accuracy Clean and sanitize lab area daily Remove subject identifying documents when assisting with remote monitoring activities. Assist clinical team with all study activities as needed. Such as vitals, EKG's, phlebotomy, etc. Maintain a safe work environment, meeting IATA and OSHA standards. Serve as a resource in lab for all team members to ensure protocols are followed. Position may require occasional weekend and/or overtime hours. Other duties as assigned Desired Skills and Qualifications: Phlebotomy experience required Lab processing experience required College graduate preferred Ability to troubleshoot lab equipment malfunctions and implement corrective actions. Familiarity with hazardous material handling and biosafety protocols. Excellent attention to detail, organizational skills, and ability to manage multiple priorities. Ability to function independently with little oversight Professional, highly motivated self-starter, and exercises initiative. Collaborative with a team mentality Ability to work fast-paced environment Organization and prioritization skills Excellent follow-up Ability to be ambulatory most of the workday. Ability to lift/transfer/push/manipulate equipment and patients, which requires strength, gross motor and fine motor coordination. AMR Clinical does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor. ** This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.

Applied Research & Technology Lab Internship (Undergraduate) LOCATION: Louisville, CO - On-Site START DATE RANGE: MAY 11 to MAY 18, 2026 | END DATE RANGE: JULY 31 to AUGUST 7, 2026 TIME COMMITMENT: 40 Hours Per Week THE ROLE: If you are looking to gain hands-on experience in a collaborative environment, learn advanced lab techniques, and contribute to meaningful research impacting patient care - join our Applied Research & Technology team for a hands-on summer internship! You'll gain experience in cutting-edge clinical diagnostics and learn how research translates into real-world healthcare solutions. WHAT YOU'LL DO: Learn to operate and assess MALDI mass spectrometry and/or cf TNA-based assays using human specimens. Explore cancer biology (hematological and solid tumors) and understand assay development for clinical diagnostics. Assist with lab workflows and ancillary duties. Analyze and synthesize experimental data, troubleshoot results, and maintain a detailed lab notebook. Present your findings to the Lab & Executive Leadership Teams at the end of the program. A Typical Day: Plan and execute experiments under the guidance of our Research Associates & Staff Scientists. Keep the lab clean and functional. Participate in team meetings and share your project updates. WHAT YOU'LL BRING: Education: Undergraduate students in MCDB, Biomedical Engineering, Biochemistry, or related fields. Coursework: Biology, genetics, or similar. Skills: Familiarity with Excel and Word, strong desire to learn. Bonus: Previous lab experience and comfort with math are helpful but not required. WHAT YOU'LL GET: Training & Support Initial 2-3 weeks entirely focused on guided training. Daily check-ins with your mentor, progressing toward independent lab work as you gain confidence. COMPENSATION Rate of $19.00 per hour DEADLINE TO APPLY: January 2, 2026 Biodesix 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, or veteran status.

Cath Lab Tech Location: Ft Mitchell, KY Agency: Care Career Pay: $3,363 per week Shift Information: Days - 4 days x 10 hours Contract Duration: 13 Weeks Start Date: 1/19/2026 AlliedTravelCareers is working with Care Career to find a qualified Cath Lab Tech in Ft Mitchell, Kentucky, 41017! Cath Lab Technicians are vital team members who assist doctors during invasive cardiovascular procedures such as angioplasty, cardiac catheterization, and electrophysiology. About Care Career Care Career is redefining what healthcare staffing can be. By uniting leading healthcare staffing brands under one network, we connect clinicians and clients to more opportunities, better solutions, and stronger support. From major health systems and MSPs to specialty clinics nationwide, our portfolio delivers the reach, resources, and expertise needed to meet today's healthcare demands with tomorrow in mind. Requirements Required for Onboarding Cath Lab Tech - Skills Core Mandatory Exam (Allied/Non-Nursing) Radiology Technologist Radiology Technologist Exam 11122039EXPPLAT

Engage with us for your next career opportunity. Right Here. Job Type: Regular Scheduled Hours: 0 This position performs Laboratory testing in the Clinical Laboratory. The Medical Technologist performs moderate and highly complex testing in the clinical laboratory, responsible for the analysis of laboratory specimens and subsequent result reporting according to laboratory protocol and procedures. Demonstrate respect, dignity, kindness and empathy in each encounter with all patients, families, visitors and other employees regardless of cultural background. Job Description: Job Duties: Understands all principle(s) involved in assigned procedures and applies this knowledge to the clinical situation or outcomes in clinical diagnosis management of the patient. (See department competency sheet.) Must be able to determine if specimen integrity issues, patient medication(s), other interfering substances that could affect patient testing results. Operates, troubleshoots and maintains laboratory equipment, supplies; and performs procedures to ensure high quality, accurate and cost effective results in all areas of the laboratory. Ensures accuracy of testing per manufacturer's guidelines and all applicable regulation. Interfaces with Hot Lines and service personnel to oversee proper functionality and repair of instruments. Reports results within time limits established for procedures, reports results for STAT, critical values and other categories as defined by Laboratory policy. Records patient data and other information quickly and accurately in the Laboratory Information Systems (LIS) and Hospital Information Systems (HIS) to ensure appropriate turnaround time and effective retrieval of patient testing results. Collects and/or processes specimens according to laboratory policies and procedures for timely and accurate testing. Performs and documents quality control as specified for each procedure meeting established internal and regulatory guidelines, accurately analyzes quality control results obtained before accepting and reporting patient testing results. Follow policies and procedures whenever tests systems are not within established acceptable levels. Notifies Supervisor or designee of discrepant quality control results Participates in Quality Assurance activities to meet the Laboratory Quality Plan. Follows policies and procedures whenever tests systems are not within established acceptable levels. Identifies problems that may adversely affect test performance or reporting of results. Initiates, investigates and implements all necessary corrective action(s). Documents follow-up in the electronic software to resolve variances in procedures and outcome(s). Must correct the problems or immediately notify the supervisor or designee. Performs proficiency testing in the same manner as patient specimens as part of the Laboratory Quality Plan. Ensures a safe environment by demonstrating knowledge of techniques, procedures and correct use of protective barrier equipment. Participates in the Laboratory Safety team to assist in Safety Audits, training and review of Laboratory Safety Policies. Enhances professional growth development of self, department staff, other hospital personnel, community and students by participation in continuing education, in-service training and the School of Medical Technology lectures and bench training. Performs all other duties as assigned. Ensures that all cost saving activities occur to meet all financial budgetary parameters and works with Supervisor/designee to ensure the most cost effective processes have been implemented, i.e. ordering reagents on time, ensuring correct orders are received, rotating stock to minimize waste, effective use of all resources to minimize waste. Performs other duties as assigned. Qualifications: Education, Credentials, Licenses: Baccalaureate Degree in a Biological Science with completion of a NAACLS approved Medical Technology program along with certification from a nationally recognized certifying agency OR Baccalaureate Degree in a Biological Science with completion of a NAACLS approved Medical Technology program along with ASCP Certification OR CLIA '88 Equivalent (HEW/HHS Certification) OR Registry Eligible - Baccalaureate Degree in a Biological Science and have completed a NAACLS accredited MT/CLS program AND be certified within a year of eligibility or be certified one year from date of hire. Registry Eligible for a Section Certification - must have a Baccalaureate Degree with a minimum of five-years technical experience in ONE of the Clinical Areas of the Laboratory. Specialized Knowledge: None Kind and Length of Experience: Minimum of 6-12 month of clinical internship as part of an approved MLS Training Program. FLSA Status: Non-Exempt Right Career. Right Here. If you're looking for the right careers in healthcare, the right place to be is at St. Elizabeth. Join us, and you'll take pride in the level of care we offer our community.

Job Title: Medical Technologist (MT/MLS) / Medical Laboratory Technician (MLT) Schedule: Tuesday-Saturday, 10:00 am - 6:30 pm Experience: CLIA, CAP Responsibilities: Perform medical laboratory tests, procedures, experiments, and analyses to provide data for diagnosis, treatment, and prevention of disease Operate and maintain laboratory equipment Follow standard operating procedures for specimen handling and processing Ensure quality control and compliance with regulations APPLY NOW! Or reach out to me directly at 617-746-2768 (accepts texts) / Megan@ka-recruiting.com. OR schedule a quick call using this link: calendly.com/megankarecruiting

All aspects of Reference Lab functions within the Main Clinic Laboratory; Phlebotomy duties on between various GGC satellite locations but only on rare occasion if necessary. Key Responsibilities: Performs phlebotomy procedures with high focus on attention to detail; properly identifying the patient prior to obtaining the specimen and accurate labeling of the specimen. Performs EKGs as well as assistance with other laboratory functions. Releasing orders from LIS on patients. Maintains the necessary precautions to follow bloodborne pathogen guidelines. Entering orders on patients in the LIS. Monitors and reports equipment functionality to appropriate personnel. May assist in orienting new employees or students regarding functions of the department. May involve some Medical Assisting duties. On occasion, may involve assisting satellite laboratory locations. Other duties as necessary or assigned Qualifications: May have 1 or more years of college or vocational or technical school training without a degree or certification AMT, ASCP, NCA or similar certification in phlebotomy helpful but not required. Demonstrates outstanding interpersonal relations and effective communication skills Must be willing to travel between satellite locations with reliable transportation. Experience in phlebotomy is highly preferred. Customer service experience highly preferred. Education: High School diploma or GED required. Certified Nursing Assistant experience helpful but not required.

Medical Solutions is seeking a travel Cath Lab Technologist for a travel job in Louisville, Kentucky. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 36 hours per week Shift: 12 hours, days Employment Type: Travel We're seeking talented healthcare professionals whose adventure game is as strong as their clinical game. Those that want flexibility and high pay, we have the positions for you! Some of the industry-leading benefits enjoyed by Medical Solutions travel nurses and travel allied healthcare professionals include: Day One Medical, Dental, and Vision with low premiums Day One 401(k) with Company Contribution Personalized Compensation Packages Paid, Private, Fully Furnished, Pet-Friendly Housing Dedicated Recruiter and 24/7 Customer Care Line Per Diem Allowance and Paid Travel Licensure and Certification Reimbursement Free Liability Coverage Voluntary Benefits: Critical Illness, Hospital Indemnity, Accident, and Pet Insurance Equal Employment Opportunity And More! Estimated pay package based on bill rate at time job was posted. Bill rates can change frequently and without notice. Exact pay package may vary based on guaranteed hours, distance being traveled, and customizations available for travelers. Medical Solutions Job ID #988271. Pay package is based on 12 hour shifts and 36 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Cardiac Cath Lab About Medical Solutions At Medical Solutions, we're people who care, helping people who care. No matter how you look at it, there's a whole lot of care going on in our world and that's just the way we like it. What do we do? Medical Solutions is one of the nation's largest providers of total workforce solutions in the healthcare industry, connecting nurses and allied health clinicians with hospitals and healthcare systems across the country and around the corner. Through our family of brands, we also serve a segment of clients outside of the healthcare space. And we're the very best at what we do. You'll love our culture that's filled with heart and soul. As a company and employer, we're sincerely and unabashedly us. We lead as humans first and believe the unique qualities of each team member make us better together. We share a purpose for helping others and the drive to make a difference. And we offer endless opportunities for personal and professional growth, throughout your career. At Medical Solutions, you'll find a great place to work and a career home. We've received Best Places to Work awards, landed top industry awards, and received accolades for the impact we've made in business and within our community. But the only way to really get to know us, is to join us. We think you'll fit right in. Benefits Weekly pay Holiday Pay Guaranteed Hours Continuing Education 401k retirement plan Pet insurance Company provided housing options Cancelation protection Wellness and fitness programs Mileage reimbursement Referral bonus Employee assistance programs Medical benefits Dental benefits Vision benefits Benefits start day 1 License and certification reimbursement Life insurance Discount program

Job Summary and Responsibilities * * Sign On Bonus up to $10,000 and Student Loan Payback up to $24,000 for Eligible Hires* Job Summary / Purpose Accurately analyzes and reports all tests ordered by the Medical Staff in a timely manner and according to laboratory procedures and regulatory guidelines to aid in the diagnosis and treatment of patients. Essential Key Job Responsibilities * Aligning with local and state requirements performs lab test procedures on patient specimens adhering to the Section's Standard Operating Procedures to ensure accurate, timely reporting. * Provides excellent patient care through clinical correlation of results, identification of patterns of bias, rapid notification of appropriate caregivers of critical values, and completion of testing within established turn-around-time limits * Ensures that major automated equipment is operational by performing required maintenance, calibration and troubleshooting procedures; including contacting of instrument vendor for assistance or repair * Performs required calibration and quality control procedures and maintains records to ensure tests are being performed within established parameters * Performs proficiency testing as assigned and review results with laboratory clinical leaders * Assists in evaluation and generation of compliant documentation for the validation of new procedures and equipment to provide the physician with the most current laboratory technology * Participates in opportunities for continuing education and/or teaching, training according to the Section Performance Standards to enhance technical skills of students, trainees, coworkers, and self * Responsible for inventory of supplies, including providing assistance with monitoring supplies, ordering, and placing received supplies into storage * Completes all work and resolves or appropriately passes ongoing issues to incoming staff within the scheduled shift * As a representative of CommonSpirit Health, utilizes professionalism and HumanKindness while communicating with physicians, hospital staff, patients, coworkers, other stakeholders in laboratory operations, and all members of the general public, whether in email, instant messaging, telephone, or face-to-face interactions * Adheres to all regulatory requirements The job summary and responsibilities listed above are designed to indicate the general nature of the work performed within this job. They are not designed to contain or be interpreted as a comprehensive inventory of all job responsibilities required of employees assigned to this job. Employees may be required to perform other duties as assigned. Job Requirements Required Education and Experience: Associate's Degree in a biological or chemical science as defined by CLIA OR High school diploma/GED and completed an official military medical laboratory course and held the military enlisted occupational speciality of Medical Laboratory Specialist (Lab Technician) Required Licensure and Certifications: Other state license not required Preferred Certification: MLT (ASCP) or equivalent certification preferred Required Minimum Knowledge, Skills, Abilities and Training: Must be appropriately trained in clinical laboratory science as judged by the Director of the Clinical Laboratory Where You'll Work Welcome to Saint Joseph London, a 150-bed regional hospital founded in 1926. Located on a 52 acre healing environment, Saint Joseph London offers private patient rooms that overlook a small lake and healing garden and has been recognized as a Best Place to Work in Kentucky for five years in a row (2020-2024). CHI Health Saint Joseph is part of CommonSpirit Health, a non-profit, Catholic health system dedicated to advancing health for all people. With approximately 175,000 team members and 25,000 physicians and advanced practice clinicians. Our commitment to serve the common good is delivered through the dedicated work of thousands of physicians, advanced practice clinicians, nurses, and staff; through clinical excellence delivered across a system of 140 hospitals and more than 2,200 care centers serving 24 states.

Family Practice Associates was founded by Dr. Jeffrey Foxx in 1983 and has grown to one of the largest family practice groups in Central Kentucky. Today FPA is a group of primary care providers who are dedicated to giving family-centered care from birth to later years. FPA has over 20 primary providers including: physicians, nurse practitioners, physician assistants, and a marriage and family therapist. With a professionally trained staff of CMA's, receptionists, lab techs and others, FPA provides award winning care that has been recognized as a Patient-Centered Medical Home (PCMH) through the National Commission on Quality Assurance. FPA works diligently to offer Central Kentucky families enhanced access to medical care at its Hamburg & Brannon Crossing locations as well as online at *************** Responsibilities The Point of Care Medical Laboratory Assistant is responsible for performing phlebotomy as well as point of care testing as part of the daily laboratory operations as assigned by the laboratory manager. These duties include (but are not limited to): Specimen collection and processing: Collecting viable and appropriate specimens from patients Maintaining the appropriate documentation for specimen collection and tracking Sending specimens to reference laboratories for any testing not performed in-house. Inventory: Maintaining adequate inventory of laboratory supplies Ensuring that all supplies are viable before use in patient testing The rotation of stock so that the oldest material is used first Safety: Guaranteeing that the safety procedures outlined in the safety manual are followed Ensuring that medical waste is properly disposed Maintaining a safe and clean work environment (waiting room, patient restrooms, phlebotomy draw areas and laboratory) Point of Care Tests: The point of care medical laboratory assistant performs only those point of care tests that are authorized by the laboratory manager and require a degree of skill commensurate with the individual's education, training or experience and technical abilities. For point of care testing, the point of care medical laboratory assistant is responsible for the following: Following the laboratory's procedures for specimen handling and processing, test analyses and reporting and maintaining records of patient test results Maintaining records that demonstrate the proficiency testing samples are tested in the same manner as patient samples. Adhering to the laboratory's quality control policies and documenting that all quality control activities, instrument and procedural calibrations, and maintenance are performed Following the laboratory's established corrective action policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance Being capable of identifying problems that may adversely affect test performance or reporting of test results and either correcting the problems or immediately notifying the technical or clinical consultant or director Documenting all corrective actions taken when test systems deviate from the laboratory's established performance specifications: Other: Any other tasks deemed appropriate and assigned by the laboratory manager Specific Requirements Phlebotomy Skills / Experience Knowledge of laboratory procedures Fine motor skills necessary to operate the computer and laboratory equipment Electronic health records experience preferred The ability to stand up most of the day, stretch repeatedly over the counter and lift loads of less than 10 pounds Good communication skills, problem solving ability, independent judgment and initiative. Ability to prioritize and develop workflow. Ability to perform other assigned tasks Must be willing to travel between both locations

Responsibilities : Performs quality control procedures to validate test results according to established standards and records results appropriately. Demonstrates the knowledge and skills necessary to provide care relevant to the patient(s) under his/her care, applying principles of growth and development over the life span. Assists in delivery of physician's reports via phone and electronic distribution in a timely manner. Responds to "technical question" calls from units and physicians. Performs preventative maintenance and monitoring of all equipment to ensure that it is working properly and maintains related records. Records on instrument logs any repairs, replacement, and maintenance needed of equipment. Maintains adequate supply inventories by rotating stock, checking for expiration dates, and ordering replacement stock. Performs venipunctures on patients of all age groups and other specimen collection using proper therapeutic skills according to procedures. Assists supervisors in additional duties which support the lab's quality program. Provides teaching and education to students and other personnel population. Qualifications: B.S.M.T, ASCP or AMT. Associates degree or higher in science required upon hire or Associates degree or higher in related field required upon hire. MLT - Certified Medical Laboratory Technician through American Society of Clinical Pathology (ASCP) required. MLT - Certified Medical Laboratory Technician through American Medical Technologists (AMT) required. Benefits Offered: 403(b) 403(b) matching Health Insurance Dental Insurance Vision Insurance Flexible Spending Account Health Savings Account Short Term Disability Cancer, Accident, Critical Illness, Hospital Indemnity Paid Vacation Time Paid Sick Time Wellness Plan

Posting Details Information Working Title Microbiology for Health Professionals Lab Part-time Instructor Department Biological Sciences Full Time or Part Time? Part - Time Position Number Purpose of Position The Department of Biological Sciences at Northern Kentucky University invites applications for part-time Instructors for Microbiology for Health Professionals Labs. This posting will be used to create a database of potential part-time faculty. Primary Responsibilities Candidates must be prepared to teach a lab section of Microbiology for Health Professionals in a fully face-to-face format on the NKU campus. Qualifications Minimum of a Master's degree in Biological Sciences with relevant microbiology experience. Completed applications will be kept on file for future opportunities. Minimum Education Master's Degree Preferred Education Posting Detail Information Requisition Number 2020F485 Job Open Date 09/24/2025 Job Close Date Quick Link ********************************** Supplemental Questions