Laboratory assistant jobs in Muncie, IN

Are you an experienced Clinical Lab Professional? If so, Labcorp wants to speak with you about exciting opportunities to join our team as a Technologist in Indianapolis, IN . In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at Labcorp: "Improving Health, Improving Lives". Work Schedule: 2nd shift - Monday - Friday 3:30pm - 11:30pm, overtime as needed. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here . Job Responsibilities Determine the acceptability of specimens for testing according to established criteria Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures Monitor, operate and troubleshoot instrumentation to ensure proper functionality Demonstrate the ability to make technical decisions regarding testing and problem solving Prepare, test and evaluate new reagents or controls Report accurate and timely test results in order to deliver quality patient care Perform and document preventative maintenance and quality control procedures Identify and replenish testing bench supplies as necessary Assist with processing of specimens when needed Maintain a safe work environment and wear appropriate personal protective equipment Requirements Bachelor's degree in Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements is required Minimum 1 year of clinical laboratory testing experience in a CLIA certified lab is required OR a MLS degree is required ASCP or AMT certification is preferred Ability to work independently and within a team environment Proficient with computers; Familiarity with laboratory information systems is a plus High level of attention to detail along with strong communication and organizational skills Must be able to pass a standardized color vision screen Flexibility to work overtime or other shifts depending on business needs 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. A dditionally, 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 .

Ready to make your next career move? VieMed Healthcare Staffing is a premier staffing agency that specializes in connecting skilled professionals with healthcare facilities, ensuring seamless continuity of care and unparalleled service delivery. We are committed to quality, reliability, and integrity for both our candidates and clients. Join us in our mission to elevate healthcare staffing to new heights. We take care of you, so you can take care of others. VHS is looking for a qualified Technician - Laboratory. City: Portland State: IN Start Date: 2025-12-29 End Date: 2026-03-30 Duration: 13 Weeks Shift: 10 Hours Overnight shift. Description: ***STRONG CERNER BECKMAN ACL TOPS AND BLOOD BANK EXP ARE REQUIRED FOR THIS POSITION*** Position / Specialty: MLT Shift: Regular schedule is 20:00-06:00 4x10s traveler will be scheduled every other weekend and weekend shift times are 17:30-6:00 National Certs REQ: ASCP - MLS or MT Years of experience REQ: 2 years First timers accepted: Yes Shift Info: Night 4x10-Hour 20:00 - 06:00 Notes: N/A W2 Pay Rate: $44.53 *Travel candidates only (50 miles or more from facility) Certification Requirements: Please confirm credential requirements with VHS upon application. At VieMed, Live Your Life isn't just a company tagline. It's a passionate commitment to improving the lives of every patient and employee. Benefits Include: Competitive Pay Packages Weekly Pay Schedule via Direct Deposit Comprehensive Medical Benefits (W-2) Robust Referral Bonus Program 24/7 Dedicated team committed to your success throughout your time with VHS Paid sick time in accordance with all applicable state, federal and local laws Licensure, certification, travel and other reimbursements when applicable **VHS is an Equal Opportunity Employer (“EEO”)/Protected Veterans/Individuals with Disabilities/E-Verify Employer and welcomes all to apply** #LiveYourLife #VHSVL

HIRING NOW: GMP Plant Quality Lab Coordinator opportunity Interested in this role? Reach out directly to Grace Williams at grawilliams @actalentservices .com | CALL/TEXT 317-567 - 6610 with an updated resume to apply The GMP Plant and Lab Quality Coordinator is responsible for ensuring the highest standards of quality across both laboratory and plant operations. This role bridges the quality lab and production plant, overseeing sample collection, testing, documentation, and compliance with internal and external standards. The coordinator plays a key role in supporting operational excellence and product integrity. Responsibilities + Collect, label, and track samples from various plant processes and incoming materials. + Prepare and distribute samples for laboratory analysis, ensuring chain-of-custody integrity. + Perform or coordinate laboratory tests on raw materials, in-process samples, and finished products. + Interpret and document test results, identifying trends or deviations from specifications. + Maintain accurate and up-to-date records of all quality activities, including test results, deviations, and corrective actions. + Prepare and review Certificates of Analysis (COAs) for outgoing products. + Ensure all quality documentation meets regulatory and customer requirements. + Develop, review, and update SOPs for sample collection, testing, and quality control processes. + Train plant and lab personnel on SOPs and quality best practices. + Support internal and external audits, ensuring compliance with ISO standards, customer requirements, and regulatory guidelines. + Participate in continuous improvement initiatives and corrective action processes. + Serve as a liaison between the plant, lab, and quality management teams. + Communicate quality issues and resolutions clearly to all stakeholders. + Promote and adhere to safe practices and sustainable operations in line with environmental and safety standards. Essential Skills + Bachelor's degree in Chemistry, Materials Science, or related field preferred. + 5+ years of experience in a quality manufacturing environment. + 5+ years of quality control, quality assurance, GMP leadership experience. + Familiarity with laboratory testing methods, quality management systems, and regulatory standards (ISO, etc.). + Lab experience related to ICP and Cytiva AKTA Chromatography. + Experience managing quality employees. + Strong organizational, documentation, and communication skills. + Ability to work independently and collaboratively in a fast-paced, innovative environment. Additional Skills & Qualifications + Experience with quality assurance, quality control, laboratory, chemistry, quality analysis, biology, audit, FDA, QC, CAPA, lab environment, batch record, biochemistry. Work Environment Work in an industrial production environment with two labs. It offers a startup/scale-up atmosphere with rapid growth opportunities and a large project with the Department of War and various other large scale projects. INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION: **INTERVIEW AVAILABILITY THIS WEEK ** + I am scheduling interviews for this position and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Grace Williams. + 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 grawilliams@actalentservices. com and/or CALL/TEXT ME: ************ Job Type & Location This is a Permanent position based out of Noblesville, IN. Pay and Benefits The pay range for this position is $90000.00 - $110000.00/yr. benefits packet provided. pto, holiday, health, dental vision, etc. Workplace Type This is a fully onsite position in Noblesville,IN. Application Deadline This position is anticipated to close on Dec 23, 2025. 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.

WinField United SureTech Lab Intern, Summer 2026 When you intern at Land O'Lakes, you're joining a Fortune 250 agribusiness and food production leader with more than 100 years of operations as a farmer- and member-owned cooperative. With business units spanning crop insight and inputs, animal nutrition, dairy foods, and sustainability solutions, you will experience a hands-on, purpose-driven internship. You'll have opportunities to network with industry leaders, tour our state-of-the-art facilities, and be challenged with a business-critical project, all while gaining skills that will impact your career trajectory. We are hiring a SureTech Lab Intern based in Indianapolis, IN for Summer 2026! SureTech is a full-service agricultural lab that provides retailers access to the timely, cost-effective, reliable data their farmers need to make better decisions. With over 50 years of experience, a dedicated team of chemists and lab technicians using the most innovative technology, and a new location with ample space and resources, SureTech has earned its reputation as a trusted partner to retailers across the U.S. As a SureTech Lab Intern you will execute laboratory experiments designed by the Technical Lead Chemist and Intern Manager. This includes test sample organization, sample handling, the running of laboratory instrumentation, and documentation and organization of experimental data. With guidance from the Technical Lead Chemist, you will participate in the analysis of the experimental data. You will be called upon to use the experimental data to draw conclusions and have an understanding of how the data can be used to drive agronomic decisions. Internship Duration: May - August 2026 Interns are paid $25.00/hour. Relocation assistance may be provided to eligible candidates for the duration of the summer internship. Experience-Education (Required) Sophomore (preferred) or Junior undergraduate pursuing a bachelor's degree in agronomy, crop & soil science, horticulture, plant biology, plant pathology, agriculture, or other related field of study. Required GPA of 3.0 or higher Competencies-Skills (Required) Ability to work without direct supervision. Excellent communication, writing, and critical thinking skills. Manage time and effectively prioritize and implement projects and general work tasks. Resourceful and innovative in finding solutions to problems. Flexible and can adapt to changing business surroundings. Ability to adhere to strict safety standards when handling crop protection products in lab and field settings. Properly wear chemical application equipment and personal protective equipment while working as required by job duties. Competencies-Skills (Preferred) Proficient in Microsoft Office Suite tools (Excel, PowerPoint) About Land O'Lakes, Inc. Join us and be part of a Fortune 250, farmer- and member-owned cooperative that is reimagining the business of food. We have been named a Top Workplace by Indeed and LinkedIn, and to the TIME 100 Most Influential Companies list. Benefits for most full-time roles include medical, dental, vision, PTO, life & disability insurance, education assistance, a 401k and a variety of well-being resources. Most part-time employees are eligible for prorated PTO, holiday pay, employee development programs, prorated education assistance, and a 401(k). Land O'Lakes, Inc. is an Equal Opportunity Employer (EOE) M/F/Vets/Disabled. The company maintains a drug-free workforce, including post-employment substance abuse testing pursuant to a Drug and Alcohol Policy. Neither Land O'Lakes, nor its search firms, will ever contact you and ask for confidential information over the phone or in email. If you receive a call or email like this, please do not provide the information being requested.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Functional Overview & Responsibilities Clinical Data Scientist Internship Overview: Each intern will be assigned to a project giving them the opportunity to contribute to ongoing analytics initiatives or help lay the foundation for new initiatives within the Data and Analytics organization. The intern will gain exposure to how analytics impacts clinical research, developing enterprise level solutions, and solving large, complex problems facing Lilly. Interns will interact and work alongside other Clinical Data Sciences professionals, including Lilly senior management. At the conclusion of the work period, each intern will present their project highlights, findings and general accomplishments to Clinical Data Sciences professionals. The role requires an in-depth understanding of programming, logic, data flow, and database architecture. Project opportunities are available in the following areas: Cloud computing Machine Learning Process automation Database development Dashboard design and development Lilly internships last for 12 continuous weeks, beginning in the last week of May. Each intern will be assigned a project affording the opportunity to learn more about data science and analytics within clinical research, as well as gain real world experience developing solutions for the Data and Analytics organization. Responsibilities during the internship may include, not limited to: Develop an understanding of processes and procedures within the Data and Analytics business unit Drive real time analytics to enable full value realization of emerging data collection modalities Ensure system validation and reliability Develops and tests new ideas and/or applies innovative solutions that create value Basic Qualifications Currently enrolled in a Master's program for Data Science, Analytics, Bioinformatics, Informatics, Mathematics, Statistics, or other relevant Technical Science with an expected graduation date of Dec. 2026 - May 2027. Additional Functional Job Skills & Preference Proficient in R or Python programming Experience in implementing ML algorithms Proven ability to work creatively and analytically in a problem-solving environment Exposure to dashboard development in PowerBI or Tableau Demonstrated teamwork and collaboration on diverse teams Additional Information All interns will be considered for full-time positions based on their internship performance Lilly arranges various intern activities including sporting events, dinners, lunch and learns, volunteer activities etc. to provide opportunities for socializing, professional development, and learning more about Lilly. Interns will receive 1 week of paid time off during the Lilly summer shut-down (June 29th, 2026 - July 3rd, 2026 1:1 mentoring from an experienced professional in the function Interns will receive a competitive salary and free parking at their work site, as well as access to Lilly's LIFE fitness center, bike garage, and many other discounts Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $43,000 - $110,000 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. 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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, a place to call home, apply with us today! Job Description Job Summary: Manage equipment maintenance and qualification activities while supporting team development and cross-functional collaboration. Key Responsibilities: Equipment Maintenance & Scheduling: Coordinate preventive and corrective maintenance with schedulers, shops, and lab personnel. Act as technical expert and troubleshoot equipment issues. Qualification & Documentation: Execute and review qualification protocols for new and existing equipment. Document activities in logbooks and electronic systems; ensure timely requalification. Process Improvement: Recommend process enhancements to improve efficiency and streamline operations. Cross-Functional Collaboration: Communicate with internal teams, external vendors, and global quality functions to align on equipment policies and operational goals. Team Leadership: Coach and develop staff, monitor workflow to meet turnaround times (TAT), conduct performance reviews, and manage training and succession planning. Best Practices & Networking: Share and implement best practices across teams related to equipment lifecycle activities. Qualifications Education & Experience: Bachelor's degree in physical sciences (e.g., chemistry, physics) 4+ years of relevant lab experience, including leadership responsibilities. Technical & Analytical Skills: Strong computer, scientific, and organizational skills. Ability to troubleshoot equipment and understand CMMS systems. Leadership & Collaboration: Proven leadership with a focus on team engagement, morale, and retention. Ability to work independently and collaboratively across teams and with external vendors. Communication & Work Style: Excellent written and verbal communication skills. Detail-oriented, self-motivated, adaptable, and able to manage multiple priorities in a fast-paced environment. Proactive and solution-oriented with strong focus on quality and productivity. Compliance & Documentation: Ability to maintain accurate records, follow instructions, and comply with company policies. Additional Information Position is full-time, 8:00 am- 5:00 pm Overtime as needed. 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 #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Job Duties/Responsibilities: Work environment/department will be listed in requirement. Determine the acceptability of specimens for testing according to established criteria. Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Demonstrate the ability to make technical decisions regarding testing and problem solving. Prepare, test, and evaluate new reagents or controls. Report accurate and timely test results to deliver quality patient care. Perform and document preventive maintenance and quality control procedures. Identify and replenish testing bench supplies as necessary. Assist with processing of specimens when needed. Maintain a safe work environment and wear appropriate personal protective equipment Requirements: Associate degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Minimum 2-4 years of clinical laboratory testing experience is required. State Medical Technician license may be required (will be listed in requirement if its needed). ASCP or AMT certification is either preferred or required (will be listed in requirement if its required). Ability to work independently and within a team environment. Proficient with computers; Familiarity with laboratory information systems is a plus. High level of attention detail along with strong communication and organizational skills. Must be able to pass a standardized color vision screen. Flexibility to work overtime or other shifts depending on business needs

* This person should provide an excellent experience for patients when collecting blood and other specimens. * May be required to work within the hospital as well as from off sites. * Registers Lab patients and enters orders from a variety of sources (electronic, written, faxed, and verbal). * Provides clerical support for all lab technical functions, maintains the physical space of the drawing area including washing glassware. * Processes specimens, including centrifuging and specimen preparation. * This position also requires interdepartmental support activities to more effectively provide patient care and flow. * These activities may range from assisting with nursing routines on non-laboratory staff and any other assigned tasks. * This individual may also perform limited waived and moderate complexity tests as authorized by the Lab Medical Director. * This position requires variable working hours starting as early as 4 am and includes weekend and holiday rotation. * This position may assist in training new staff and will perform other duties as assigned. QUALIFICATIONS: JOB SPECIFIC CORE COMPETENCIES: * Expert phlebotomy and customer services skills. * Accurately sort and process all types of body fluids, tissues while maintaining high degree of accuracy. * Performs POC testing. * General understanding of medical terminology and keyboarding experience. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES: * Must be skilled at blood collections and have general phlebotomy experience. * Must have previous healthcare experience or understand basic medical terminology and have keyboarding experience. * This position requires the ability to move rapidly from location to location within the hospital. * This position requires the ability to accurately sort and distribute all types of body fluids, tissues, and other specimens brought to the lab for analysis. * This position requires maintaining a high level of accuracy while simultaneously performing a variety of tasks. * Requires the employee to travel from work to collect specimens remote from the hospital. * Must have a valid Indiana driver's license and a vehicle to make these trips under various climatic conditions if the hospital vehicle is not available. * Must be contactable by telephone for backup coverage. * Must maintain competency per protocol and attend applicable continuing education. EXPECTED BEHAVIORS: * Must possess the qualities of integrity and good judgement. * Must maintain good physical and emotional well-being. * Must be able to communicate technical information clearly both in direct conversation and by phone. * Must have a consistently friendly, reassuring personality in dealing with patients. * Must have strong interpersonal skills for maintaining good relationships with clients. * Must have good typing skills. * Experience with computers a plus. Must maintain qualities agreed to in Patients First Commitment (Attitude/Demeanor, Respect, Teamwork, Accountability/Initiative, Communication and Dedication to Excellence). LICENSURE/CREDENTIAL REQUIREMENTS: Phlebotomy certification preferred or previous phlebotomy experience. ADDITIONAL EDUCATION AND EXPERIENCE REQUIREMENTS: Phlebotomy certification preferred and/or phlebotomy training from post-secondary school, High School Diploma and valid Indiana Driver's License. PHYSICAL/MENTAL DEMANDS: * Assist ambulatory patients independently * Hearing requirements include but are not limited to hearing and responding to codes, monitors, pagers, phones, equipment alarms or patients calling for assistance, ability to auscultate B/P. * Manual dexterity, as used for performing intricate procedures (catheter, dressing changes, IV starts), assembling medical equipment, caring for patients, typing, etc. * Standing, walking, stooping, kneeling, and crouching as needed more than 2/3 of day EQUIPMENT USED: Phlebotomy tools and equipment. ENVIRONMENTAL CONDITIONS: Exposure to biohazardous fluids and tissue. Exposure to toxic and noxious chemicals. There is also a risk of injury from various sharp objects routinely used in performing laboratory procedures

Versiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our donors, and provide the science behind the medicine through our diagnostic laboratories. Versiti brings together outstanding minds with unparalleled experience in transfusion medicine, transplantation, stem cells and cellular therapies, oncology and genomics, diagnostic lab services, and medical and scientific expertise. This combination of skill and knowledge results in improved patient outcomes, higher quality services and reduced cost of care for hospitals, blood centers, hospital systems, research and educational institutions, and other health care providers. At Versiti, we are passionate about improving the lives of patients and helping our healthcare partners thrive. Position Summary Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . Total Rewards Package Benefits Versiti provides a comprehensive benefits package based on your job classification. Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO) and Holidays, Short- and Long-term disability, life insurance, 7% match dollar for dollar 401(k), voluntary programs, discount programs, others. Responsibilities Understand and perform to all applicable regulatory and compliance requirements. Perform testing, as scheduled. Support sample evaluation and processing, as needed. Perform on-call, weekend, and holiday work, as scheduled. Perform reagent preparation, as scheduled. Operate, troubleshoot, and perform routine maintenance and calibration on equipment. Support customer inquiries via phone, email, and lab information system (LIS). Support the maintenance of reagent and supply inventory. Maintain sample integrity and ensure proper identification of all specimens. May participate in validations. May support training, as assigned. Maintain organization of departmental records, as needed. May assist in educating fellows, residents, students, and visitors to the laboratory. May support preparation or management of proficiency samples in the laboratory. May release results in accordance to training and compliance requirements. Review daily work for accuracy and escalate as appropriate. May provide support for transfusion product selection, as applicable. Performs other duties as required or assigned which are reasonably within the scope of the duties in this job classification Understands and performs in accordance with all applicable regulatory and compliance requirements Complies with all standard operating policies and procedures Qualifications Education Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical technology, or related field. required Associate's Degree in a laboratory science or medical laboratory technology from an accredited institution. required Knowledge, Skills and Abilities Ability to read and interpret documents such as Standard Operating Procedures, safety rules, operating and maintenance instructions, and other department manuals. Must have basic mathematical aptitude. Ability to apply judgment to detailed and structured written or oral instructions. Ability to organize work to provide efficient and productive workflow. Flexibility to work independently and with a team. Must have strong attention to detail. Must have basic communication skills. Possess legible handwriting. Tools and Technology Personal Computer (desktop, laptop, tablet). required General office equipment (i.e. computer, printer, fax, copy machine). required Microsoft Suite (Word, Excel, PowerPoint, Access, Outlook). required Software systems (including but not limited to Customer Relationship Management Software, Laboratory Information Systems, Learning Management System). required Lab/department specific equipment, including, but not limited to: required Pipettes (single channel, multi-channel, electronic, etc.). required Centrifuges, freezers, refrigerators. required pH meter, microscopes, balances. required Flow Cytometry based equipment required Spectrophotometer required qPCR Instrumentation required Thermal Cycler required Gel Electrophoresis required Sequencer required Aggregometer required Automated instruments (hematology counter, DNA isolator, plate washer, Coagulation analyzer, etc.). required Not ready to apply? Connect with us for general consideration.

Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries. Why Arcwood? * Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves. * Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges. * Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant, Always. * Collaborative Environment: Together we can achieve much more. Join a supportive and dynamic team where your ideas and efforts are recognized and rewarded. Our Commitment: We are dedicated to fostering an inclusive and innovative workplace where every employee can thrive. As part of our team, you will have the freedom to contribute your expertise wherever needed, ensuring the success of our mission to protect the environment. Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet. Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future. Laboratory Supervisor As the Laboratory Supervisor you will be responsible for overseeing the facility's laboratory function to ensure that tests are performed accurately, according to regulations and in a timely manner. Essential Functions & Requirements: * Prioritizes health and safety by adhering to policies, processes, and maintaining safe practices at all times * Supervises the laboratory and laboratory personnel to ensure the accurate, compliant, and productive operations of the department * Reviews analytical data to confirm data accuracy and acceptability of material for disposal * Provides oversight of the redirection and testing of off-spec materials * Coordinates additional testing with third-party laboratories or other service providers as needed * Manages the purchases and distribution of departmental operating supplies; ensures adherence to laboratory budget to promote profitability and performs functions to control costs * Provides technical expertise as needed to the Operations and Sales teams; supports Sales by ensuring pre-acceptance testing is completed appropriately * Supports, maintains and troubleshoots various laboratory instruments and equipment * Prepares various reporting as requested by location or organizational leadership * Participates in hiring, performance evaluation, promotion and discipline decisions for team members as needed * Takes on additional duties as assigned to support the team and organization Education: * Bachelor's degree (required); degree in chemistry or science-related field (preferred) Experience: * 3+ years of progressive experience in a laboratory environment (required) Competencies: * Hands-on approach to effectively complete testing, equipment maintenance and training * Strong communication skills to effectively and timely communicate details of questionable or hazardous materials to appropriate authorities, respond to incidents, and train other laboratory personnel * Chemical knowledge including characteristics, reactions and hazards of substances encountered in the hazardous waste industry * Strong computer skills including Microsoft Office Suite applications * Working knowledge of Laboratory Information Management (LIM) systems * Strong time management and multi-tasking skills * Detailed understanding of regulatory requirements and familiarity with industry trends * Ability to effectively troubleshoot and conduct maintenance on laboratory equipment * Regular and predictable attendance to perform the functions and requirements of this role Benefits, Compensation, & Workforce Diversity: Arcwood offers competitive pay and bonus incentives. Benefits include choice of medical, dental, and vision plans, flexible spending or health savings accounts, employee and dependent life insurance, short and long-term disability, 401(k) savings plan with 7% company match, and tuition reimbursement. Equal Opportunity Employer - Veterans & Disabilities A post-offer drug screen and background check will be required.

Indiana University Health is Indiana's most comprehensive health system, with 16 hospitals and more than 34,000 team members serving Hoosiers across the state! We're looking for team members who are inspired by challenging and meaningful work for the good of every patient. People who are compassionate and serve with a purpose. People who aspire to excellence every day. The laboratories of IU Health offer some of the most comprehensive laboratory services in Indiana! Open 24 hours a day, seven days a week, the laboratories perform more than 19 million tests a year. In addition to IU Health, laboratory testing services are provided to hospitals and physicians across the country. SHIFT: Full-Time, Evening The Lab Assistant II at LAB provides general laboratory services including specimen collection, blood component preparation, pre-analytic processing of specimens, waived testing and identified moderate complexity testing as well as related clerical tasks. The incumbent may be responsible for patient and specimen registration and delivery of specimens. Requires HS grad or GED Equivalent. Requires successfully completion of an initial and six (6) month competency for identified testing. Requires successfully completion an annual competency assessment for identified testing. Completion of a phlebotomy training program with experience in laboratory or coursework in biological, chemical or related science preferred. Experience in waived or moderate complexity is preferred. Requires working knowledge of computers. Requires telephone skills. Requires ability to perform repetitive tasks for prolonged periods of time. May serve on appropriate committees or projects that contribute to the overall purpose and essential functions of the department. As Indiana's largest and most comprehensive healthcare system, and the number 1 ranked healthcare system in Indiana, we offer: Increased pay scale for bedside nurses. 401(K) retirement savings with employer match Tuition reimbursement Student loan forgiveness - Government program that may allow qualifying participants to have the remainder of their student loan balance forgiven (after a set amount of time and specific qualifications have been met). Employee Assistance Program - Counseling at no cost to you Healthy Results - Participation in our team member wellness programs award points that contribute toward a biweekly financial incentive in your paycheck! The more you participate, the more you earn!

We are seeking a self-motivated Chemistry Lab Technician to join our Lab Operations team. In this role you will assist in laboratory confirmatory analysis of biological fluids including urine, oral fluid (saliva) or hair specimens. This role is also responsible for operating, maintaining and troubleshooting various Auto Chemistry instrumentation. Shift: 03:00 - 11:30pm Salary: $20.00 per hour Primary Responsibilities Loads, prepares and extracts specimens using various Auto-Chem Instrumentation. Assist in instrument calibration, QC review, and initial analytical review. Prepare reagents and buffers as needed. Assists with maintaining an adequate inventory of laboratory supplies. Responsible for all record keeping associated with specimen preparation, including following chain of custody handling guidelines and storage requirements. Conducts safe work practices according to safety protocols, PPE requirements and decontamination procedures. Responsible to maintain all safeguards as it pertains to Protected health information (PHI). Qualifications Bachelor's degree in a science field (Chemistry, Biochemistry, Biology, Microbiology, Pre-med (Biomed), required. Experience as a lab technician, preferred utilizing LCMS equipment. Data entry skills via a keyboard (alpha and numeric) required. Strong eye-hand coordination. Ability to handle a high-volume environment while maintaining the highest level of quality, required. Physical demands required to perform critical tasks in this role include standing for long periods of time, lifting up to 25lbs, bending and carrying. Benefits Cordant supports our employees by providing a comprehensive benefits package to eligible staff (per state regulations) that includes: Medical, Dental, Vision Insurance, Flexible Spending Accounts (FSA), Health Savings Accounts (HSA) Paid Time Off (PTO) accruing on day 1, Volunteer Time Off (VTO), Paid Holidays, 401(k) with Company Match, Employee Assistance Program (EAP), Short Term and Long-Term Disability (STD/LTD) and Company Paid Basic Life Insurance. #LAB123

Pay Range: Responsible for laboratory testing, quality control, phlebotomy, instrument maintenance and troubleshooting. Perform manual and automated routine blood tests. Prepare specimens for microscope examination. Operate laboratory equipment including centrifuges, dry bath incubators, and blood bank refrigerators. Key Performance Areas Responsible for performing proper quality control procedures before proceeding with patient testing. Ensure that proper documentation including test report logs, quality control logs, equipment records, and all lab procedure and training checklists are completed on the correct time schedule. Will be responsible to ensure this is performed in central lab. Maintain adequate inventory of laboratory supplies. Place order with purchasing as needed. Perform technical laboratory procedures with accuracy and precision, meeting the standard of all accreditation/regulatory agencies. Perform instrument maintenance at the required times and as needed. Initiate troubleshooting procedures when instrument malfunction occurs and contact instrument service company, if necessary. Comply with established safety guidelines and maintains cleanliness of the laboratory and equipment. Complete any and all duties required to keep laboratory in compliance with state and federal regulatory agencies. Must be able to perform compliance testing. Maintain and ensure the confidentiality of all patient and employee information at all times. Comply with all Federal and State laws and regulations pertaining to patient care, patient's rights, safety, billing, and collections. Adhere to all AON and departmental policies and procedures, including IT policies and procedures and the Disaster Recovery Plan. Must maintain MLT license and required CEUs. Assist in training new employees to related job duties. Will be expected to work overtime when given sufficient notice of required overtime. Qualifications Education A.A. or A.S. degree License and Certification Appropriate state license required. National lab certification preferred. BLS preferred. Experience Minimum of four years experience in the healthcare field, preferably in a clinical setting is required. #AONC #LI-ONSITE

Requirements QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty competently. The requirements listed below are representative of the knowledge, skill and/or ability required CERTIFICATES, LICENSES, REGISTRATIONS: N/A LANGUAGE SKILLS: Above average communication skills in English especially via telephone MATH SKILLS: Basic Math skills COMPUTER SKILLS: Basic Microsoft Products, Data Entry, Internet Ability to use and learn proprietary software systems Education and Experience: Minimum requirements for education and experience for this position High School or Equivalent (GED) 1 to 2 years of experience ENVIRONMENTAL CONDITIONS: The work environment characteristics described here are representative of those employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Potential exposure to blood and body fluid: Performs tasks which involve exposure to blood, body fluid, or tissue. PHYSICAL DEMANDS: The physical demands described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Lift/Carry - 26-75% Push/Pull - 26-75% Reach Overhead - 0-25% Climb - 0-25% Squat/Bend/Kneel - 0-25% Sit - 26-75% Stand - 76-100% Walk/Move About - 76-100%

Cath Lab Tech Location: Carmel, IN Agency: Windsor Healthcare Recruitment Group, Inc. Pay: $2,550 per week Shift Information: Days - 3 days x 12 hours Contract Duration: 13 Weeks Start Date: ASAP AlliedTravelCareers is working with Windsor Healthcare Recruitment Group, Inc. to find a qualified Cath Lab Tech in Carmel, Indiana, 46032! Scrub experience is preferred Minimum Experience Required: 1 YEAR REQUIRED, 1st time travelers accepted if they have 3+ years of experience Shift: 4x10s, block scheduling TBD with the call requirement, it could mean being on call on a day off** Call Required: Minimum 2 days a week and every 3rd weekend Dailey Census - 5-7 Documentation: Cerner, McKesson Certifications: ACLS, BCLS Equipment: Mckesson-Hemo Balloon Pumps Angio Jet CSI diamondback Penumbra Inari Roto pro Jet stream- BSCI C-arms: Philips/Siemens ACIST MEDRad power injector Temp Pacer- Medtronic IVUS Abbott - OCT Skills: Circulate, Conscious Sedation required Procedures: Cardiac - LHC, RHC, Balloon pumps, Temp pacer, Perm pacer/defib, pericardial effusion, STEMI call. IR - venous access, drains placement, GI tube insertion, PE, DVTs, Tips, PV, Fistula work, UFEs, prostate embos, GI/Post Partum/other internal bleeds Effective 11/30/24, IU Health will not allow IN RN s to work at their facilities (SEE EXCEPTIONS BELOW). **Periop/OR RN s, Allied and Ambulatory RN travelers are exempt from this rule. These IN travelers are allowed to work past the 11/30 deadline. Periop includes ENDO, IR RN, PACU, Cath Lab RN, SDS** About Windsor Healthcare Recruitment Group, Inc. WHR isn't just another staffing agency - we're a tightly-knit family committed to empowering healthcare professionals to not just find jobs, but to carve out fulfilling careers. When you choose to partner with us, you unlock a world of opportunities. 10952651EXPPLAT

HIRING NOW: GMP Plant Quality Lab Coordinator opportunity Interested in this role? Reach out directly to Grace Williams at grawilliams @actalentservices .com | CALL/TEXT 317-567 - 6610 with an updated resume to apply The GMP Plant and Lab Quality Coordinator is responsible for ensuring the highest standards of quality across both laboratory and plant operations. This role bridges the quality lab and production plant, overseeing sample collection, testing, documentation, and compliance with internal and external standards. The coordinator plays a key role in supporting operational excellence and product integrity. Responsibilities * Collect, label, and track samples from various plant processes and incoming materials. * Prepare and distribute samples for laboratory analysis, ensuring chain-of-custody integrity. * Perform or coordinate laboratory tests on raw materials, in-process samples, and finished products. * Interpret and document test results, identifying trends or deviations from specifications. * Maintain accurate and up-to-date records of all quality activities, including test results, deviations, and corrective actions. * Prepare and review Certificates of Analysis (COAs) for outgoing products. * Ensure all quality documentation meets regulatory and customer requirements. * Develop, review, and update SOPs for sample collection, testing, and quality control processes. * Train plant and lab personnel on SOPs and quality best practices. * Support internal and external audits, ensuring compliance with ISO standards, customer requirements, and regulatory guidelines. * Participate in continuous improvement initiatives and corrective action processes. * Serve as a liaison between the plant, lab, and quality management teams. * Communicate quality issues and resolutions clearly to all stakeholders. * Promote and adhere to safe practices and sustainable operations in line with environmental and safety standards. Essential Skills * Bachelor's degree in Chemistry, Materials Science, or related field preferred. * 5+ years of experience in a quality manufacturing environment. * 5+ years of quality control, quality assurance, GMP leadership experience. * Familiarity with laboratory testing methods, quality management systems, and regulatory standards (ISO, etc.). * Lab experience related to ICP and Cytiva AKTA Chromatography. * Experience managing quality employees. * Strong organizational, documentation, and communication skills. * Ability to work independently and collaboratively in a fast-paced, innovative environment. Additional Skills & Qualifications * Experience with quality assurance, quality control, laboratory, chemistry, quality analysis, biology, audit, FDA, QC, CAPA, lab environment, batch record, biochemistry. Work Environment Work in an industrial production environment with two labs. It offers a startup/scale-up atmosphere with rapid growth opportunities and a large project with the Department of War and various other large scale projects. INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION: INTERVIEW AVAILABILITY THIS WEEK * I am scheduling interviews for this position and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to Grace Williams. * 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 grawilliams@actalentservices. com and/or CALL/TEXT ME: ************ Job Type & Location This is a Permanent position based out of Noblesville, IN. Pay and Benefits The pay range for this position is $90000.00 - $110000.00/yr. benefits packet provided. pto, holiday, health, dental vision, etc. Workplace Type This is a fully onsite position in Noblesville,IN. Application Deadline This position is anticipated to close on Dec 23, 2025. 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.

Discover more at Labcorp as we help you take ownership of your personal and professional development, provide continuous learning opportunities and empower you to grow beyond the boundaries of your career. We are hiring a Supervisor, Microbiology to join our growing team in Indianapolis, IN! What to Expect: Directly oversees and is responsible for the technical work of the department; responsible for the operational readiness of equipment, instruments and personnel necessary to meet the daily delivery of testing services. Meets client expectations in delivery of testing services. Essential Job Duties: * Managerial and Leadership duties and responsibilities: * Supervises the day to day production and nonproduction activities of the local departmental employees. * Directly monitors the quality of testing services provided by employees under his/her supervision. * Assigns appropriately trained personnel and ensures sufficient number of staff are available to complete the workload. Supervision: * Schedules department personnel appropriately to match the demands of the daily workflow with in the supervised area. * Provides direct supervision to employees, including assignments, technical and behavioral performance counseling, and troubleshooting. * Schedules and supervises all non-production activities and obligations of her/his area, such as validations, surveys, etc. * Provides support as required to the department manager to assist in the fulfillment of his/her responsibilities, including acting as manager, upon delegation, during absences. Performance Monitoring and Evaluation: * Assures quality and timely performance of both production and non-production activities under supervision. o Reports performance and results against targets and global standards. * Ensures regulatory compliance within his/her supervision. * Communicates all production and non-production standards, guidelines and information to the supervised staff. * Ensures on-time delivery of performance reports (PT, QC/PM, Internal and External QC) and responses to inquiries from other functional areas. o Participates in and supports client visits, audits and inquiries, as necessary, to ensure complete fulfillment of requests and interests. Personnel: * Recruits, trains, and contributes to retention efforts of employees. * Conducts technical training and development of staff as needed. * Supports the departmental manager in assessing and meeting the resource needs. * Supports the development of plans to meet future resource needs. * Evaluates the performance of employees. * Works with department manager to establish training plans for the supervised staff. * Supports the manager in employee evaluations and development plans. * Essential External Client-related Job Duties: * Supports marketing and sales as needed in their efforts to meet specific client requests for testing services. Other: * Perform other duties as required, including testing of patient samples in areas of competence. Experience and Education: Minimum Required: Earned a Bachelor's degree and has had 4 years of experience in a laboratory following clinical training; prior supervisory or management experience is a plus. A licensed physician or has earned a doctoral degree in a biological, chemical, or physical science and after graduation, has had at least two years of post-baccalaureate pertinent laboratory training and experience equivalent to that of an ASCP certified medical technologist, in a clinical laboratory having a director at the doctoral level. OR Earned a Master of Arts or science degree in a biological, chemical, or physical science and subsequent to graduation has had at least two years of post-baccalaureate pertinent laboratory experience and training equivalent to that of an ASCP certified medical technologist, of which not less than two years have been spent working in the designated specialty in a clinical laboratory having a director at the doctoral level. OR Meets qualifications for a technologist and has at least four years of post-baccalaureate pertinent laboratory experience equivalent to that of an American Society of Clinical Pathologists (ASCP) certified medical technologist, of which not less than two years has been spent working in a clinical laboratory having a director at the doctoral level. Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. 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.

ESSENTIAL DUTIES AND RESPONSIBILITIES: *Handling of bodily fluids including blood, urine, feces, etc. *Data entry including organizing of patient requisitions, accessioning samples into the laboratory information system and double-checking work for accuracy. *Basic computer knowledge and some data entry experience is a requirement. *Understand technical and non-technical procedures required to process and forward accessioned specimens to the designated laboratory location for testing. *Maintain processing refrigerator and freezer temperature logs. *Maintain processing centrifuges and logs. *Responsible for checking-in all Couriers and receiving samples. *Assist Phlebotomists with labeling of samples if needed. *Must be able to adjust to increased workloads. *Must be able to periodically lift or move biohazard waste bins which could weigh more than 20 lbs. *Able to locate and pull specimens from refrigerated storage as needed or requested. * Learns and keeps familiar with lab procedures and policies. *Other duties as assigned. Requirements QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty competently. The requirements listed below are representative of the knowledge, skill and/or ability required CERTIFICATES, LICENSES, REGISTRATIONS: N/A LANGUAGE SKILLS: Above average communication skills in English especially via telephone MATH SKILLS: Basic Math skills COMPUTER SKILLS: Basic Microsoft Products, Data Entry, Internet Ability to use and learn proprietary software systems Education and Experience: Minimum requirements for education and experience for this position High School or Equivalent (GED) 1 to 2 years of experience ENVIRONMENTAL CONDITIONS: The work environment characteristics described here are representative of those employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Potential exposure to blood and body fluid: Performs tasks which involve exposure to blood, body fluid, or tissue. PHYSICAL DEMANDS: The physical demands described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Lift/Carry - 26-75% Push/Pull - 26-75% Reach Overhead - 0-25% Climb - 0-25% Squat/Bend/Kneel - 0-25% Sit - 26-75% Stand - 76-100% Walk/Move About - 76-100%

Cath Lab Tech Location: Carmel, IN Agency: Windsor Healthcare Recruitment Group, Inc. Pay: $2,935 per week Shift Information: Days - 3 days x 12 hours Contract Duration: 13 Weeks Start Date: ASAP AlliedTravelCareers is working with Windsor Healthcare Recruitment Group, Inc. to find a qualified Cath Lab Tech in Carmel, Indiana, 46032! Minimum Experience Required: 2 YEARS REQUIRED, 1st time travelers accepted if they have 3+ years of experience Shift: 4x10s Certifications: ACLS, BCLS, ARRT, RCIS Equipment: Acist injector, Siemens C-arm, Philips C-arm, Medrad power injector, Rotopro, Diamondback, IVUS, OCT, Shock wave, Rampart, Pneumbra, Inari Skills: Circulate, Conscious Sedation required Procedures: Cardiac - LHC, RHC, Balloon pumps, Temp pacer, Perm pacer/defib, pericardial effusion, STEMI call. IR - venous access, drains placement, GI tube insertion, PE, DVTs, Tips, PV, Fistula work, UFEs, prostate embos, GI/Post Partum/other internal bleeds Effective 11/30/24, IU Health will not allow IN RN s to work at their facilities (SEE EXCEPTIONS BELOW). **Periop/OR RN s, Allied and Ambulatory RN travelers are exempt from this rule. These IN travelers are allowed to work past the 11/30 deadline. Periop includes ENDO, IR RN, PACU, Cath Lab RN, SDS** About Windsor Healthcare Recruitment Group, Inc. WHR isn't just another staffing agency - we're a tightly-knit family committed to empowering healthcare professionals to not just find jobs, but to carve out fulfilling careers. When you choose to partner with us, you unlock a world of opportunities. 10787883EXPPLAT