Laboratory technician jobs in Mack, OH - 283 jobs

HIRING NOW: Quality Laboratory Tech Interested in this role? Reach out directly to Max Richey at ***************************** | CALL/TEXT 317-567 - 6591 with an updated resume to apply The Quality Lab Technician is responsible for performing routine and specialized physical, chemical, and microbiological testing of raw materials, finished products, and associated items to ensure compliance with company, regulatory, and customer quality standards. This role supports production by providing timely and accurate data, maintaining laboratory equipment, and documenting results in accordance with food safety, SQF, HACCP, GMP, and other regulatory requirements. The technician plays a key role in continuous improvement initiatives, collaborating with production and quality teams to maintain product integrity and safety. Responsibilities Conduct microbiological, chemical, and physical testing on raw materials, finished products, and mixes. Perform specialized testing including FOSS FT-120, CEM analysis, and plating for SPC, Coliform, yeast, and mold. Record, analyze, and report test results, promptly addressing deviations or non-conformities. Maintain and calibrate laboratory equipment, ensuring schedules are followed. Assist in investigations related to product quality or process deviations. Follow sanitary procedures and food processing quality control methodologies. Standardize mixes and collect line samples to ensure consistency and compliance. Collaborate with production and quality teams to support product safety and continuous improvement. Assist in developing and validating new testing methods and procedures. Adhere to GMP, safety regulations, and company policies at all times. Perform multiple tasks simultaneously, including lifting up to 50-pound dairy cases or boxes, and working long hours on feet. Accomplish other duties as assigned to support laboratory and production operations. Essential Skills Bachelor's degree in Food Science, Microbiology, Chemistry, or related scientific discipline preferred. Alternatively, a high school diploma or 2-year college studies in microbiology, chemistry, or lab sciences with 1-2 years of laboratory or quality assurance experience in dairy, aseptic manufacturing, food manufacturing, or related industry. Experience with microbiological and chemical testing methods required. Familiarity with food safety and quality standards including SQF, HACCP, and GMP. Strong attention to detail and analytical skills with ability to form sound conclusions and initiate corrective actions. Excellent communication and teamwork abilities to work effectively in cross-functional teams. Ability to thrive in a fast-paced environment and manage multiple tasks simultaneously. Additional Skills & Qualifications * Proficiency in laboratory techniques such as pipetting, wet chemistry, titration, and using equipment like HPLC. * Experience in quality control and assurance in a manufacturing environment. INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION: I am scheduling interviews for this position ASAP and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Max Richey HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to mrichey @actalentservices. com or CALL ************ * Job Type & Location This is a Permanent position based out of Richmond, IN. Pay and Benefits The pay range for this position is $43160.00 - $43160.00/yr. Company Offers: Pro rated PTO and personal time Paid holidays and additional compensation if having to work the holiday Health Benefits Dental Vision 401k Workplace Type This is a fully onsite position in Richmond,IN. Application Deadline This position is anticipated to close on Jan 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Work Schedule 12 hr shift/days Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials Job Description Compensation: $21.75/HR Shift: Thursday - Saturday Days - 6:00am - 6:30pm Shift Differential: +10% Location: Cincinnati, OH - 2110 East Galbraith Road As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Join our Pharma Services team and be a part of a leading contract development and manufacturing organization (CDMO) offering end-to-end services for drug development, clinical trial logistics, and commercial manufacturing! Biotech and biopharma companies trust us for our speed, flexibility, and quality across every phase of drug development. Our Drug Product team supports customers in the formulation, production, and packaging of high-quality drug products! Our dedicated colleagues offer a wide range of services, including formulation development, process optimization, scale-up, fill-finish services, packaging, and labeling. Their efforts ensure the efficient production of various drug products, such as sterile injectables and oral dosage forms. Location/Division Specific Information: The Cincinnati, OH site is a Center of Excellence for specialized oral solid dose manufacturing and drug development within the Pharma Services Group. How Will You Make an Impact?: As a Formulation Technician you will be responsible for performing operations related to the manufacturing of pharmaceutical products through equipment set-up, operation, clean up and maintenance in compliance with all regulatory cGMP requirements and company policies and procedures. A Day in the Life: Accurately follows production documents, standard operating procedures (SOP's) and current good manufacturing practices (cGMPs) Maintains consistent and accurate documentation of activities to include batch production, cleaning, assembly, material transportation, and waste disposal. Follow approved batch records (BPR's), clean up sheets, and equipment assembly sheets. Safely operates computer-controlled equipment used in dispensing, granulation, compression or coating. Disassembles, cleans, and re-assembles equipment using basic hand tools to include mixers, extruders, dryers, tablet press, encapsulation, coating pans, printers, or tablet inspection machines. Education: High school diploma or equivalent required. Experience: Preferred: Previous work experience in manufacturing, operations, production or lab setting or related field Preferred: Experience in a cGMP environment Knowledge, Skills, Abilities: Mechanical aptitude/proficiency and ability to disassemble and reassemble various types of equipment (GMP facility preferred) Basic reading comprehension and math skills to follow sophisticated technical instructions and complete BPR calculations. Ability to maintain compliance in all SOP, cGMP, EHS and other training curriculum as assigned. Physical Requirements / Work Environment: Manipulate/handle materials, equipment, tools, up to 100 lbs and lift containers weighing up to 40 lbs. Position requires wearing personal protective equipment to include white zone gowning requirements and various styles of respirators (1/2 face, 3-M hood, full face, and dust mask). Hand-scoop 5 lbs. intermittently throughout the workday. Operate a stand up fork lift and walkie stacker What We Offer: Compensation: Competitive Hourly Pay Rate! Additional shift differential for 2nd shift and 3rd shift positions Annual performance-based bonus Annual merit performance-based increase Excellent Benefits: Benefits & Total Rewards | Thermo Fisher Scientific Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Designated Paid Holidays 401K Tuition Reimbursement Employee Referral Bonus Career Advancement Opportunities

Environmental Enterprises, Inc. is a specialty environmental management and disposal company. We are dedicated to protecting the environment by providing quality environmental services, recycling options, and waste disposal at competitive rates through innovative technologies and superior technical support. We strongly support improving the quality of life for our employees and the community. We are currently looking to fill the challenging and rewarding position of Lab Pack Chemist This is an entry level position that involves working both indoors and outdoors at our customer's sites. This is NOT a laboratory position. The field chemist is responsible for preparing containers for pick up, including identification of chemicals, lab packing hazardous and non-hazardous chemicals at customer locations. Limited travel including overnight stays (~10%). DETAILS OF ASSIGNMENT: Moving and preparing containers (pails, drums, viles) for transport Identification of chemicals Packing hazardous and non-hazardous chemicals at customer locations Other duties as requested by Field Services Manager and corresponding team members. Requirements At times, the field technician may be required to wear a full or half face respirator, SCBA, or air lines. Ability to routinely lift 60 pounds, with occasional lifting in excess of 60 pounds. Insurable driving record. Willingness to obtain a class B CDL with hazmat endorsement within the first year preferred. High school graduate required. 2-year degree in chemistry or other natural sciences highly preferred. The field technician is OSHA HAZWOPER 24-Hour trained. Typically, the work is conducted in Level D but sometimes conditions warrant Level B or C personal protective equipment. Some travel may be necessary for this position. The field technician is capable of taking direction, working well with others, and decision-making. Additional skills required for this position are provided below. Safety oriented Observant Resourceful Versatile A post offer drug screen and background check will be required. Learn more about the great things we do at: ************** Environmental Enterprises Inc. is an Equal Employment Opportunity (EEO) employer and does not discriminate on the basis of race, color, national origin, religion, gender, age, veteran status, political affiliation, sexual orientation, marital status or disability (in compliance with the Americans with Disabilities Act) with respect to employment opportunities. Full Time; Monday to Friday 8 AM to 4:30 PM 40 hours weekly

Responsibilities * Prepare samples according to project protocol and/or related SOPs; * Maintain compliant laboratory documentation; * Perform data analysis and data checking; * Interpret results obtained for accuracy and acceptability; * Clean and sterilize laboratory equipment; and * Other duties deemed necessary. Qualifications * A minimum of a Bachelor's degree, with previous experience in a research laboratory; * Knowledge of GLP, cGMP, and ICH guidelines; * Strong organizational and communication (written and oral) skills; and * Knowledge of Microsoft Word, Excel, and Powerpoint. Travel: None Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks * Cincinnati Campus Overview * Flexible work environment * Competitive PTO packages, starting at 20+ days * Competitive compensation and benefits package * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Community involvement with local nonprofit organizations * Discounts on local sports games, fitness gyms and attractions * Modern, ecofriendly campus with an on-site fitness center * Structured career paths with opportunities for professional growth * Discounted tuition for UC online programs Awards * Named a Top Workplace in 2024 by The Cincinnati Enquirer * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Are you organized, accountable, and have always gone the extra mile to make sure things are done right? Imagine the impact those skills can have in ensuring the accuracy of millions of healthcare tests, every month. If you share our passion for strengthening physician care, please apply for this onsite Clerk position! LabCorp is seeking a dedicated and motivated individual to join their Specimen Processing and Accessioning team in City, State. The position, Hospital Reference Test Clerk, will be responsible for performing clinical specimen accessioning, sample sorting and data entry in a fast-paced, high-throughput environment located onsite with one of our client offices. **Pay Range: $17.75 - $25.92 per hour All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data Work Schedule: Monday - Friday 8:00am - 4:30pm Work Location: TCH 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. Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, please click here. Job Responsibilities: Prepare laboratory specimens for analysis and testing Communicate effectively with client office staff · Research, troubleshoot and resolve customer and specimen problems Meet department activity and production goals Data entry of patient information in an accurate and timely manner Accurately identify and label specimens Pack and ship specimens to proper testing facilities Scrub requisitions to ensure samples are prepared and missing items are updated Do spinning/freezing/splitting and other special services as needed based on client Requirements: · High School Diploma or equivalent · 1 year relative experience required (lab/accessioning, production/manufacturing/warehouse environment) · Previous medical or patient facing healthcare experience is a plus · Comfortable handling biological specimens · Ability to accurately identify specimens · Experience working in a team environment · Strong data entry and organizational skills · High level of attention to detail · Proficient in MS Office · Ability to lift up to 40lbs. · Ability to pass a standardized color blind test If you'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 our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

Part Time Contract Role | Lab/Research Technician in Mason OH Duration: 4 months contract with possible extension Pay Range: $18 -20/hour on w2 Part Time: 20-25 hours/week Responsible for managing the flow of product samples within the laboratory, ensuring accurate logging, assessment, and data entry. This role is central to supporting research and development activities by maintaining rigorous standards in sample handling and evaluation, and by providing reliable data to inform product development and quality assurance. Key Responsibilities: Sample Logging: Receive and log all incoming samples, ensuring each is accurately recorded in the laboratory tracking system. Maintain clear records of sample origin, type, and relevant metadata. Lab-Based Assessment: Conduct standardized laboratory assessments on samples, following established protocols for physical, or performance testing. Document all procedures and results meticulously. Data Entry: Enter assessment results and relevant observations into designated spreadsheets or databases, ensuring data integrity and traceability. Continuous Improvement: Identify opportunities to streamline sample handling and evaluation processes, contributing to lab efficiency and data quality. Skills to Have and/or Expect to Learn Experience with laboratory sample management and evaluation protocols Attention to detail in logging and data entry Familiarity with spreadsheet software (e.G., Excel) for data recording and analysis Ability to follow and refine lab procedures Strong organizational and communication skills Growth mindset and willingness to learn new lab techniques Qualifications: Researcher Level 1, part-time (20-25 hours/week) Demonstrated ability to manage priorities and deliver results on time Ability to collaborate effectively within a team Strong analytical and organizational skills

What You'll Do Perform moderate and high complexity testing, as defined by CLIA, while following the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of test results Stay current on and adhere to all laboratory policies and procedures. Properly document all deviations and/or corrective actions taken per laboratory policy Demonstrate competency at least annually as outlined by laboratory procedures Ensure laboratory compliance with CAP by participating in proficiency testing in accordance with laboratory procedures Aware of regulatory requirements and performs studies to ensure those requirements are met at predefined intervals Assist in preparing for and participate in inspections/audits as needed Proficiently utilize key software systems in the lab to ensure accurate and timely reporting of patient results Operate laboratory equipment and perform routine equipment maintenance, including quality controls. Identify, diagnose, and repair issues that may arise Exercise good documentation practices in accordance with laboratory policies Identify and address problems that may adversely affect test performance or reporting of test results and notify/ consult with the appropriate members of laboratory management Uphold CTI's mission and values through accountability, innovation, integrity, quality, and teamwork Other duties as assigned by management What You Bring Ability to work in a regulated environment Ability to follow procedures with great attention to detail Ability to effectively communicate Ability to think critically and problem solve basic issues Ability to prioritize and drive results with a high emphasis on quality Ability to work as part of a team Ability to multitask with excellent attention to detail Bachelor's degree in a science or health-related field (chemical, physical, biological, or clinical laboratory science or medical technology) Certification from a recognized accrediting body ( i.e. ASCP) At least 3 years of experience with moderate and/or high complexity testing CRO or Clinical Research Trial experience preferred Experience with Laboratory Information Management System (LIMS) preferred Working knowledge of CAP/CLIA, with knowledge of GCP and GLP preferred Why CTI? We support career progression - 25% of our global staff is promoted annually and we have a structured mentoring program to provide the support you need to move forward We value education and training - We provide tuition reimbursement, partner with universities and colleges to create programs in our field, and have a dedicated training department We value our people - We have never had a layoff in our 20-year history, support a work-life balance with flexible schedules, and have provided cash bonuses every year for the past decade Our culture is unparalleled - Click here to learn more about "The CTI Way" We think globally and act locally - We have a global philanthropic program supporting our team's efforts to improve their local communities (Click here to learn more about our "CTI Cares" program) Important Note In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from **************** email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (***************** or from our verified LinkedIn page. Please Note We will never communicate with you via Microsoft Teams or text message We will never ask for your bank account information at any point during the recruitment process Equal Opportunity Employer/Veterans/Disabled

Full-time Description The Lab Assistant is responsible for receiving all specimens in the Accessioning Department and preparing specimens for testing. This includes entering incoming specimens into the Laboratory Information System (LIS), pipetting specimens to the required test tubes, preparing specimens for testing, and restocking supplies in a high-throughput production laboratory environment where work is assessed based on speed and accuracy. This position requires a high level of attention to detail. Monday-Friday, 7:00AM-3:30PM. Receive incoming urine, oral fluid, and blood specimens; open, count, and sort specimens Ensure specimen integrity by verifying that specimens are labeled appropriately and that identifying information on the specimen matches identifying information on accompanying documentation and/or electronic orders Enter patient data, specimen information, medication lists, ordered tests, and point-of-care results into the LIS - manual data entry may be required for some specimens Correctly identify specimens that do not meet criteria for testing and specimens that need to be placed on hold for missing information Print barcode labels and attach appropriately to specimen containers, test tubes, and to any documentation Pipet (aliquot) accessioned urine specimens into appropriate test tubes to prepare for testing and storage Meet established Key Performance Indicators (KPIs) for speed and accuracy Transport accessioned specimens to other departments in a timely manner to prepare for testing Stock and refill samples, reagents, and supplies for lab operations throughout the day Scan documentation into the LIS Document specimens that do not meet criteria for testing and notify other departments Assist with preparing specimens for rerun testing Dispose of urine and oral fluid specimens that have reached their retention date Communicate effectively with other departments about issues regarding specimen processing Clean storage bins and carts as needed Other duties as assigned Requirements EDUCATION AND EXPERIENCE REQUIREMENTS High school diploma or GED required Minimum of 1 year of data entry experience required Preference for candidates with familiarity with drug names and HIPAA-protected information Preference for candidates with experience working with bodily fluids, such as urine, oral fluid, and blood KNOWLEDGE, SKILLS, AND ABILITIES Skill with completing assignments accurately, and with attention to detail Skill in data entry with minimal errors Ability to analyze, organize, and prioritize work while meeting multiple deadlines Ability to communicate effectively, orally and in writing Ability to function in a team environment and promote collaboration Must be able to work under limited supervision where the work assignments are subject to established procedures, techniques, and well-defined policies PHYSICAL REQUIREMENTS Work will be performed in a laboratory environment and exposes the incumbent to normal laboratory hazards and chemicals, including biohazard materials Work in varying degrees of temperature (heated or air conditioned) Accessioning of specimens requires sitting/standing for up to 4 hours continuously Position requires sitting, walking, standing, reaching, bending, stooping, and handling objects with hands and/or fingers, talking and/or hearing, and seeing Must be able to lift up to 50 lbs.

Engage with us for your next career opportunity. Right Here. Job Type: Regular Scheduled Hours: 0 This position performs medical diagnostic testing and specimen processing in the Clinical Laboratory. The Medical Laboratory Technician performs waived, moderate and highly complex testing under the supervision of a Medical Technologist or General Supervisor and is responsible for the analysis of laboratory specimens and subsequent result reporting according to laboratory policies 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: Position is stationed on a 2nd shift weekend rotation and 2 holidays a year with flexibility. Understand basic principle(s) involved in assigned procedures. Evaluates specimens for acceptability for proper testing. Investigates and documents problems with unacceptable specimens. Understands special handling requirements for test results that meet outlying criteria. Performs and documents instrument maintenance as scheduled in assigned area(s), performs and documents calibration according to scheduled intervals or receipt of reagents, trouble-shoots instruments as assigned by supervisor or designee. 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 to ensure appropriate turnaround time and effective retrieval Collects specimens according to laboratory policies and procedures for timely and accurate testing. Performs and documents/records quality control as specified for each procedures meeting established internal and regulatory guidelines. Participates in Quality Assurance activities to meet quality improvement standards. Performs proficiency testing in the same manner as patient specimens. Ensures all incidents that do not meet standard operating procedures are documented in the appropriate QA software for follow-up and investigation. Cleans, organizes and stocks lab work stations so work can be performed in a safe and orderly manner and follows all Safety policies and procedures, i.e. personal protective clothing, face shields, etc. Enhances professional growth development of self, department staff, other hospital personnel, community and students by but not limited to, participation in continuing education and in-service training. Complies with established laboratory and hospital policies for universal precautions and safety procedures. Safety policies and procedures will be followed when using chemicals, blood or body fluids, follows all MSDS requirements for any chemical or reagent, disinfects laboratory benches, properly disposes of hazardous waste, reports safety hazards to the appropriate supervisor. Attends all required Safety training programs, describes his/her responsibilities related to general safety, departmental safety and specific job related hazards. Participates in required Fire Drills or other safety related processes as determined by the department or organization. Ensures a safe environment by demonstrating knowledge of techniques, procedures and correct use of protective barrier equipment Performs other duties as assigned. Education, Credentials, Licenses: Associate's Degree in a Relevant Science with technician training program in a school accredited/approved by HHS or MLT eligible under Medicare/CLIA regulation(s) and has certification from a nationally recognized certifying agency as a Medical Laboratory Technician OR Associate's degree in a Relevant Science with completion of a technician training program in a school accredited/approved by HHS or MLT eligible under Medicare/CLIA regulation(s) with ASCP Certification OR If Registry Eligible - Associate's Degree and has completed a Medical Laboratory Technician training program in a school accredited/approved by HHS or MLT eligible under Medicare/CLIA regulation(s) and must be certified within a year of eligibility or be certified one year from date of hire. OR Be a high school graduate or equivalent who successfully completed an official military medical laboratory course of (50) weeks and have held the military enlisted occupational specialty of (Medical Laboratory Specialist (Laboratory Technician) with ASCP Certification. Kind and Length of Experience: Minimum of four months clinical internship as part of an approved 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.

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: - Covington and Ft. Thomas locations 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.

I'm hiring for a Med Tech in Ohio! There is a 20k sign-on bonus. The Med Tech performs complex lab tests essential for diagnosing, treating, and preventing a variety of medical conditions. The Med Tech will use critical thinking as you evaluate and solve problems related to biological specimens that you analyze, and you will provide interpretation of those tests. Location: Near Amsden, OH Type: Full-time and permanent Shift: Nights, Mon-Fri Requirements: College degree; ASCP cert; prior experience Pay: 54k-87k/yr Benefits: 401k; health, dental, and life insurance; PTO, etc. Offering My clients are offering a competitive compensation and benefits package (PTO, health insurance, etc.), with potential for sign-on bonus and/or relocation assistance! There are many opportunities for growth with this company. To apply, 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#LM7682 Medical Technologist, Medical Laboratory Technician, Medical Laboratory Scientist, Clinical Laboratory Scientist, MT, MLT, MLS, CLS, Med Tech, Laboratory, Medical Laboratory Ohio, Amsden, Fostoria, Arcadia, Bloomdale, Risingsun, West Millgrove, Bascom, Bettsville, Alvada, New Riegel

HIRING NOW: Quality Laboratory Tech Interested in this role? Reach out directly to Max Richey at ***************************** | CALL/TEXT 317-567 - 6591 with an updated resume to apply The Quality Lab Technician is responsible for performing routine and specialized physical, chemical, and microbiological testing of raw materials, finished products, and associated items to ensure compliance with company, regulatory, and customer quality standards. This role supports production by providing timely and accurate data, maintaining laboratory equipment, and documenting results in accordance with food safety, SQF, HACCP, GMP, and other regulatory requirements. The technician plays a key role in continuous improvement initiatives, collaborating with production and quality teams to maintain product integrity and safety. Responsibilities + Conduct microbiological, chemical, and physical testing on raw materials, finished products, and mixes. + Perform specialized testing including FOSS FT-120, CEM analysis, and plating for SPC, Coliform, yeast, and mold. + Record, analyze, and report test results, promptly addressing deviations or non-conformities. + Maintain and calibrate laboratory equipment, ensuring schedules are followed. + Assist in investigations related to product quality or process deviations. + Follow sanitary procedures and food processing quality control methodologies. + Standardize mixes and collect line samples to ensure consistency and compliance. + Collaborate with production and quality teams to support product safety and continuous improvement. + Assist in developing and validating new testing methods and procedures. + Adhere to GMP, safety regulations, and company policies at all times. + Perform multiple tasks simultaneously, including lifting up to 50-pound dairy cases or boxes, and working long hours on feet. + Accomplish other duties as assigned to support laboratory and production operations. Essential Skills + Bachelor's degree in Food Science, Microbiology, Chemistry, or related scientific discipline preferred. + Alternatively, a high school diploma or 2-year college studies in microbiology, chemistry, or lab sciences with 1-2 years of laboratory or quality assurance experience in dairy, aseptic manufacturing, food manufacturing, or related industry. + Experience with microbiological and chemical testing methods required. + Familiarity with food safety and quality standards including SQF, HACCP, and GMP. + Strong attention to detail and analytical skills with ability to form sound conclusions and initiate corrective actions. + Excellent communication and teamwork abilities to work effectively in cross-functional teams. + Ability to thrive in a fast-paced environment and manage multiple tasks simultaneously. Additional Skills & Qualifications + Proficiency in laboratory techniques such as pipetting, wet chemistry, titration, and using equipment like HPLC. + Experience in quality control and assurance in a manufacturing environment. INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION: + I am scheduling interviews for this position ASAP and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Max Richey + HOW TO APPLY DIRECTLY: Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to mrichey @actalentservices. com or CALL ************ + Job Type & Location This is a Permanent position based out of Richmond, IN. Pay and Benefits The pay range for this position is $43160.00 - $43160.00/yr. Company Offers: Pro rated PTO and personal time Paid holidays and additional compensation if having to work the holiday Health Benefits Dental Vision 401k Workplace Type This is a fully onsite position in Richmond,IN. Application Deadline This position is anticipated to close on Jan 30, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Environmental Enterprises, Inc. is a specialty environmental management and disposal company. We are dedicated to protecting the environment by providing quality environmental services, recycling options, and waste disposal at competitive rates through innovative technologies and superior technical support. We strongly support improving the quality of life for our employees and the community. We are currently looking to fill the challenging and rewarding position of Lab Pack Chemist This is an entry level position that involves working both indoors and outdoors at our customer's sites. This is NOT a laboratory position. The field chemist is responsible for preparing containers for pick up, including identification of chemicals, lab packing hazardous and non-hazardous chemicals at customer locations. Limited travel including overnight stays (~10%). DETAILS OF ASSIGNMENT: Moving and preparing containers (pails, drums, viles) for transport Identification of chemicals Packing hazardous and non-hazardous chemicals at customer locations Other duties as requested by Field Services Manager and corresponding team members. Requirements At times, the field technician may be required to wear a full or half face respirator, SCBA, or air lines. Ability to routinely lift 60 pounds, with occasional lifting in excess of 60 pounds. Insurable driving record. Willingness to obtain a class B CDL with hazmat endorsement within the first year preferred. High school graduate required. 2-year degree in chemistry or other natural sciences highly preferred. The field technician is OSHA HAZWOPER 24-Hour trained. Typically, the work is conducted in Level D but sometimes conditions warrant Level B or C personal protective equipment. Some travel may be necessary for this position. The field technician is capable of taking direction, working well with others, and decision-making. Additional skills required for this position are provided below. Safety oriented Observant Resourceful Versatile A post offer drug screen and background check will be required. Learn more about the great things we do at: ************** Environmental Enterprises Inc. is an Equal Employment Opportunity (EEO) employer and does not discriminate on the basis of race, color, national origin, religion, gender, age, veteran status, political affiliation, sexual orientation, marital status or disability (in compliance with the Americans with Disabilities Act) with respect to employment opportunities.

The Medical Technologist at Medpace Reference Laboratories plays a pivotal role in research based drug development within the pharmaceutical industry. Due to our recent growth, we are in need of qualified and focused driven individuals, like yourself. You would have the unique opportunity to work on the laboratory side of the fast paced medical world by conducting routine and esoteric testing on blood, tissue, and body fluids. If you have an analytical mind set, and enjoy working in a team-oriented laboratory setting, this could be the opportunity for you! We are hiring for the following shifts: * 8:30 AM - 5:00 PM * 10:00 AM - 6:30 PM * 11:30 AM - 8:00 PM Responsibilities * Perform low, moderate, and high-complexity testing * Train on state-of-the-art instrumentation to learn maintenance and troubleshooting skills * Evaluate and interpret quality control and testing results * Problem solve and work alongside our team of Medical Laboratory Scientists and PhD Scientists to develop and validate new tests and methods for routine and biomarker testing in our expanding laboratory * Strictly adhere to safety procedures Qualifications * A Bachelor's degree with MT, MLS, or CLS (ASCP) certification, or certification eligible; or * Bachelor's degree with MLT(ASCP) certification or certification-eligible * Previous experience in a laboratory setting a plus Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks * Cincinnati Campus Overview * Flexible work environment * Competitive PTO packages, starting at 20+ days * Competitive compensation and benefits package * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Community involvement with local nonprofit organizations * Discounts on local sports games, fitness gyms and attractions * Modern, ecofriendly campus with an on-site fitness center * Structured career paths with opportunities for professional growth * Discounted tuition for UC online programs Awards * Named a Top Workplace in 2024 by The Cincinnati Enquirer * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Engage with us for your next career opportunity. Right Here. Job Type: Regular Scheduled Hours: 36 💙 Why You'll Love Working with St. Elizabeth Healthcare At St. Elizabeth Healthcare, every role supports our mission to provide comprehensive and compassionate care to the communities we serve. For more than 160 years, St. Elizabeth Healthcare has been a trusted provider of quality care across Kentucky, Indiana, and Ohio. We're guided by our mission to improve the health of the communities we serve and by our values of excellence, integrity, compassion, and teamwork. Our associates are the heart of everything we do. 🌟 Benefits That Support You We invest in you - personally and professionally. Enjoy: - Competitive pay and comprehensive health coverage within the first 30 days. - Generous paid time off and flexible work schedules - Retirement savings with employer match - Tuition reimbursement and professional development opportunities - Wellness, mental health, and recognition programs - Career advancement through mentorship and internal mobility Job Summary: Under the direction of the General or Section Laboratory Supervisor, performs specimen processing functions, waived and moderate complexity testing as defined by CLIA Section 493.1421 and as approved by the Medical Director, and other non-technical duties as assigned. Demonstrate respect, dignity, kindness and empathy in each encounter with all patients, families, visitors and other employees regardless of cultural background. Job Description: Prepares, packages, labels, and sends out specimens as directed by procedures. Generates appropriate worksheets for reference laboratory specimens and prepares specimens to be sent to reference lab. Receives specimen from pneumatic tube system, responsible for centrifuging blood and urine specimens as needed. Centrifuge blood and urine specimens for analysis. Aliquot specimens and prepare for analysis. Performs waived and moderately complexity testing as defined by CLIA. Reports testing according to established protocols including evaluation of specimen acceptability Provides support functions to technologist including the loading and maintaining instruments, assist in re-constituting reagents, thawing, pooling, of blood products. Receives, logs in specimens (i.e., urines, blood specimens, and body fluids) from inpatient nursing units, outpatients, and operating rooms and Emergency Department. Transports specimens from Central Processing Area to each laboratory section. Files specimens once testing is complete, locates any specimens that have “add on “ testing Checks unfinished work report and daily checklist if needed. Supports the Central Processing staff when needed, i.e. receiving specimens, answering the telephones, etc. Follows recommended procedures for universal precautions and safety policies, as established in the Laboratory. Decontaminates work area daily. When handling blood or body fluids, follows universal precaution procedures in order to minimize exposure to infectious diseases. Assists in the Maintenance and repair of clinical laboratory equipment within the scope of training. Performs clerical support duties necessary to ensure efficient running of laboratory section or general laboratory. Completes all mandatory competencies and training modules along with review of all departmental policies and procedures and must adhere to all safety policies and procedures. Performs other duties as assigned to facilitate the efficient and cost effective operation of the laboratory that fall within their scope of practice. Shall follow and demonstrate knowledge of applicable safety and health rules, guidelines, and procedures as outlined in the SEMC Safety and Infection Control Manual; and perform work-related duties in compliance with local, state, and federal regulations. The associate must be able to demonstrate the knowledge and skills necessary to provide services based on the applicable principles of growth and development over the life span. Performs other duties as assigned. Performs other duties as assigned. Education, Credentials, Licenses: High School graduate or GED Specialized Knowledge: Computer skills Human relations and communication skills. Customer service skills Kind and Length of Experience: 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.

This is a fully onsite role based at our Global Central Laboratory in Highland Heights, KY. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. Available Shifts: 2nd Shift: Thursday-Sunday, 12PM ET-10:30 PM ET 2nd Shift: Wednesday-Saturday, 12PM ET-10:30 PM ET 2nd Shift: Friday-Monday, 12PM ET-10:30 PM ET ** Work hours on Sundays for 2nd shift are 10AM-8:30PM ET 1st Shift: Monday-Friday with a rotating Saturday, 6AM-2:30PM ET At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Our Clinical Diagnostics teams are trusted partners for in vitro diagnostic (IVD) companies, offering innovative solutions for drug testing, laboratory quality control, sepsis diagnosis, prenatal screening, and more. As a Lab Assistant in our clinical chemistry group, you'll play a crucial role in supporting these efforts and advancing healthcare. DESCRIPTION: As a Lab Assistant in our clinical chemistry group, you will support the daily operations of our state-of-the-art laboratory. Your work will contribute to the development and delivery of diagnostic solutions that healthcare professionals rely on to make informed decisions. You'll be part of a team that's committed to accuracy, quality, and innovation in clinical diagnostics. What You'll Do: • Process and manage clinical samples for various diagnostic tests • Assist in the preparation of reagents and materials for clinical chemistry assays • Maintain laboratory equipment and ensure compliance with regulatory standards • Contribute to the efficient functioning of our lab services by performing essential support tasks • Collaborate with a diverse team of scientists and healthcare professionals Education and Experience: • High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification • Technical positions may require a certificate • Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year) or equivalent combination of education, training, & experience. Years of experience refer to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions. Knowledge, Skills and Abilities: • Effective communication skills • Good cooperative and collaborative skills • Attention to detail • Ability to adhere to laboratory policies and standard operating procedures • Data recording skills • Ability to work in a collaborative team environment Working Conditions and Environment: • Work is performed in a clinical environment. • Exposure to biological fluids with potential exposure to infectious organisms. Physical Requirements: • Frequently stands, twists waists, squats, and bends neck for 4--6 hours per day. • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. • Frequent mobility required. • Occasional crouching, stooping, bending and twisting of upper body and neck. • Moderate lifting (or otherwise movement, carrying, setting, and placement)of 15-30 lbs. with a maximum lift of 35 lbs. • Ability to access and use a variety of computer software developed both in-house and off-the-shelf. • Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. • May interact with others, relating and gathering sensitive information. Interaction includes diverse groups. • Works with guidance or reliance on oral or written instructions from management. May require periods of intense concentration. • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task. • Regular and consistent attendance. Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience - and where your contributions truly make a difference. Apply today to help us deliver tomorrow's breakthrough.

Engage with us for your next career opportunity. Right Here. Job Type: Regular Scheduled Hours: 36 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. 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: 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.

Medpace Reference Laboratories is currently seeking Laboratory Receiving Assistants to work in our Sample Management/Biorepository Department. This individual will be responsible for basic administrative duties as well as the handling and delivery of clinical samples and other materials. 8:00-4:30 PM Saturday Shift Required Responsibilities * Receive biological samples; * Perform sample processing duties (unpack samples, scanning samples, data entry, etc.); * Handle dry ice; and * Prepare sample shipments to be sent to third-party lab * Participate in clinical study projects to facilitate testing timelines and deliverables * Assist with routine maintenance and/or cleaning of equipment * Performs sample retrieval and QC of physical inventory for study-related projects, transfers/shipments, general inventory upkeep, and to maintain database accuracy * Adheres to good documentation practices, and ensures accurate database entry of sample- or subject-related demographics * Communicates professionally with inter-functional groups regarding daily business, project-specific requests, or problem resolution * Coordinates with management, project staff, and other team members to execute assigned responsibilities in a timely manner. Qualifications * High school diploma or equivalent; * Basic computer skills; * Prior sample management, logistics, or health care experience desired; and * Team-worker and detail-oriented with good time management skills. Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks * Cincinnati Campus Overview * Flexible work environment * Competitive PTO packages, starting at 20+ days * Competitive compensation and benefits package * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Community involvement with local nonprofit organizations * Discounts on local sports games, fitness gyms and attractions * Modern, ecofriendly campus with an on-site fitness center * Structured career paths with opportunities for professional growth * Discounted tuition for UC online programs Awards * Named a Top Workplace in 2024 by The Cincinnati Enquirer * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Environmental Enterprises, Inc. is a specialty environmental management and disposal company. We are dedicated to protecting the environment by providing quality environmental services, recycling options, and waste disposal at competitive rates through innovative technologies and superior technical support. We are currently looking to fill the challenging and rewarding position of Chemical Treatment Technician . We are seeking dependable individuals with strong work ethic, willingness to learn and take initiative . Full time benefits include: Excellent health coverage, dental, vision, life and disability insurance Paid vacation & sick time Six paid holidays 4o1(k) match Paid company provided training. First shift Monday-Friday, competitive pay at a stable company! PRIMARY TASKS: Load, unload, process hazardous and nonhazardous chemical waste materials at a permitted waste treatment facility independently or with supervision. PHYSICAL DEMANDS (non-inclusive): This position is physical in nature and requires: walking, standing, climbing, bending, reaching, lifting (up to 70 pounds), carrying, pushing/pulling, and twisting. This position involves working with and around chemicals & environmental contaminants. Work is performed in outdoor and indoor environments and workers are subject to heat and cold while donning required PPE. At times, the technician may be required to wear a respirator, supplied air and full protective suit. DETAILS OF ASSIGNMENT: Processing of hazardous chemical waste safely in accordance with company procedures and EPA, DOT and OSHA regulations Moving drums, including safe operation of a fork truck Utilize barcode system to Review laboratory data to determine proper handling and disposal of materials Responsible for keeping operating areas, walls, pipes and floor in a clean and safe condition Perform chemical compatibility checks to prevent reactions and other issues Performs work in a safe manner, following all safety procedures QUALIFICATIONS: High school diploma or equivalent One year applicable experience 24 or 40 Hour Hazwoper certificate preferred Be able to communicate clearly, both verbally and in writing Environmental Enterprises Incorporated is an Equal Opportunity Employer M/F/Disabled/Vets