The Laboratory Technician II is responsible for the accurate and timely processing of biological samples , and for ensuring that the results of the tests they perform are of high quality and are interpreted correctly. This role also prepares dosing formulations and drives development and troubleshooting in this area. Work ranges from the use of standard formulation techniques to exercising technical judgment. They also contribute to data review and equipment qualification. *This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range is $26-$31/hr will adjust along with the level of the role to match the person's relevant experience and/or education le Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Key Accountabilities Processes biological specimens for Good Laboratory Practices (GLP) and Non-GLP studies including but not limited to: blood, plasma, serum, synovial fluid, urine, feces, and saliva. Completes in-house clinical assays including but not limited to: clinical chemistry, hematology (complete blood count (CBC), reticulocytes, coagulation), and urine sample analysis using automated analyzers. Prepares slides and performs microscopic cell counts and differential counts for blood and other biological fluids. Creates appropriate study records for collecting, processing, analyzing, and storing samples. Prepares labels for biological sample collection and storage tubes according to study protocol requirements . Receives chemical test articles and vehicles from study sponsors, logs in and appropriately stores (e.g. room temperature, refrigerator, freezer, etc.). Maintains storage conditions and records for test article reser Documents use and disposition of test article. Coordinates shipments of test articles, samples or other items as needed. Prepares detailed Chain of Custody (COC) for study sample or return test material shipments and files completed COCs when returned from the Sponsor. Complies with Department of Transportation (DOT) Hazardous Materials shipping requirements. Complies with international shipping regulations/documentation when applicable. Monitors and records storage conditions (freezer/refrigerator storage units and room temperature storage areas) for GLP and non-GLP test article reserve. Maintains inventory and tracks laboratory supplies for expiration dates. Apprises management of problems beyond the scope of own knowledge and expertise. Lab Equipment Maintains chemistry, hematology and urine analyzers, and any other necessary clinical pathology instrumentation and equipment. Creates and maintains current equipment identification labels. Performs appropriate maintenance, calibration and quality control on clinical pathology equipment. Maintains calibration testing records on all laboratory equipment including balances, centrifuges, calibration weights, pH meter, hoods, etc. Formulations Prepares control/test article formulations for use in Good Laboratory Practices (GLP) and non-GLP studies. Interacts with Study Director to understand the formulation instructions and assure that the appropriate chemicals/solutions have been received from the sponsor, or that they have been ordered to do the formulation. Prepares appropriate study records for formulation of test article and vehicle, as needed. Assures all chemistry data incorporated into study report is complete and accurate. Performs monthly inventory of chemicals/drugs and disposal of expired items. Receives and maintains Certificate of Analysis (CoA) and Safety Data Sheet (SDS) for chemicals stored in the lab. Appropriately stores and disposes of hazardous waste in accordance with local regulations and Environmental Health and Safety (EHS) requirements. Formulation Development Maintains knowle ge of modifications and developments in chemical techniques and procedures. Researches, develops, and validates new formulation methods. Assists in developing and writing formulation procedures for use in GLP and non-GLP studies. Suggests and assists in developing refinements to chemical techniques and procedures in use. Other Follows all Standard Operating Procedures (SOPs) and other applicable laboratory or company policies and procedures. Maintains confidential information. Supports and participates in company initiatives as directed. Performs periodic review of all applicable SOPs to ensure accuracy and confirm procedures are being performed according to SOPs. Participates in SOP writing, review, and revision, as needed. Completes training requirements as assigned and maintains appropriate training documentation. Maintains compliance and adheres to all safety regulations, policies, and procedures and good documentation practices. Maintains a thorough knowledge and ensures compliance with GLP, United States Department of Agriculture (USDA), Association of Assessment and Accreditation of Laboratory Animal Care (AAALAC), Office of Laboratory Animal... For full info follow application link. Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, gender, gender identity, sexual orientation, physical or mental disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.