We have an exciting opportunity for upcoming grads to join our Clinical Pathology Services team in Greenfield, IN!

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions-because we know that knowledge has the potential to make life better for all. Here, you can apply your scientific curiosity in Biology, Animal Science, Zoology, Animal Behavior, Veterinary Technology, Dairy Science, Equine Science or similar majors to pursue advances in animal welfare and research the effectiveness, safety and toxicity of drugs in early development animal research studies. Your work will help medical, biotech, and pharmaceutical companies create life-saving vaccines and medicines that make a real impact on people's lives. #LifeatLabcorp

• Schedule: 1st shift Monday-Friday operations, with weekend on-call once they are proficient.

• Perform assigned clinical laboratory testing accurately and in a timely manner.
• Retrieve and check specimens against pending list. Document and resolve any specimen discrepancies. Notify Lab manager when specimen discrepancies are not resolved
• Prepare workstation and instrumentation for the assigned testing.
• Receive, open and place in service all reagents according to SOPs.
• Prepare and properly label reagents and document according to SOPs.
• Operate instruments to perform testing in accordance with established written procedures.
• Resolve routine and non-routine assay problems.
• Perform parallel testing, reagent validation, linearity's, and stability studies.
• Process and ship samples according to study specific instructions.
• Evaluates and solves problems related to the collection and processing of specimens.
• Ensure the validity of test results through the performance of established quality control procedures. Interpret quality control results according to established departmental procedures.
• Prepare quality control material accurately.
• Document quality control results. Check for and acknowledge biases, warnings, and violations of control rules.
• Reports the quality control results to the management, troubleshoots, and takes corrective action on questionable or out-of-limit results. Documents all corrective actions and submits them for review by the management.
• Prepare proper documentation of test results and enter into the information system.
• Generate an appropriate audit trail for all activities.
• Document and report any result reporting problems or inconsistencies to laboratory management.
• Complete testing within the expected turnaround time to meet customers' expectations.
• Perform maintenance on instruments and equipment daily, weekly, monthly, and document.
• Calibrate instruments / assays as required and document.
• Ensure that maintenance is performed and documented according to SOP.
• Perform basic instrument and equipment troubleshooting.
• Notify laboratory management when an instrument or equipment does not meet specifications.
• Comply with regulatory guidelines, Universal Precautions and Covance Standard Operating Procedures (SOPs) at all times.
• Participates in proficiency testing and maintains a record of on-going competency along with personal training file.
• Maintain a clean, organized and safe work environment. Handles hazardous materials, reagents and chemicals in a safe manner according to SOP.
• Exercises and maintains levels of competence, integrity and interpersonal skills necessary to attain regulatory and quality goals.
• Supports and participates in Corporate and Department initiatives regarding quality system implementation, maintenance, and continuous quality improvement activities.
• Serve as clinical pathology team member for Labcorp studies.

• Work primarily 1st shift
• Work rotating weekends, holidays and overtime with supplementary compensation
• Enjoy 24 days of personal-time-off (PTO) (pro-rated depending on start date)
• Benefits: 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. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable. For more detailed information, pleaseclick here.

• Formal and informal mentoring opportunities
• Extensive training and job shadowing opportunities
• Personalized development planning
• Exposure to many drug development scientific career paths

• Bachelor degree and completion of at least 12-month training program in Medical Technology OR
• Bachelor degree in a chemical, physical or biological science from an accredited college or university AND on year training and/or experience in the specialty in which testing is to be performed. Such training must be equivalent to that received in a school of Medical Technology.
• Ability to perform basic computer skills (e.g. Word, Excel, Outlook, LIS)
• One year of experience working in the Medical Technology field.