GENERAL STATEMENT OF RESPONSIBILITY: Perform duties related to sample preparation, submissions, and/or data review with strict adherence to departmental procedures; work in compliance to departmental safety requirements consistent with good laboratory practices.
ESSENTIAL FUNCTIONS:
• Receive and separate samples; verify proper chain of custody, prioritize re-preps, determine prep dilutions, create batch worksheet and labels, prep samples for drugs of abuse.
• Monitor, maintain, clean, calibrate, and record needed documentation on equipment; manual single and multi-channel pipettors, balance, heat blocks, refrigerator, freezer, temperature monitoring system, glassware.
• Operate, monitor, maintain, calibrate, troubleshoot, and record needed documentation on instrumentation; Tecan, LC/MS/MS, ICS, Headspace, microplate reader, microplate washer.
• Proper material labeling, pipetting of controls and samples, transfer and enter sequences onto designated instruments for analysis, loading of samples on to instruments.
• Maintain and distribute supplies; preparing reagents, re-filling troughs, re-furbishing materials needed for sample prep, keep work area neat and clean, following departmental clean up procedures in disposal of hazardous chemicals and waste.
• Comply with safety regulations, proper use and handling of equipment and materials.
• Read and follow laboratory SOP’s.
• Meet qualitative and quantitative production goals of the department.
• Monitor pass-through, request samples as needed, prioritize and assign batches as needed.
• Communicate with department members to ensure maximum production.
• Notify QA/QC of low reagents, low controls, and target range discrepancies.
Notify management of needed supplies; assist with maintaining an inventory of consumables and receiving and stocking supplies.
• Monitor instrument run status, review calibration, quality control and patient samples in accordance to chromatography acceptance criteria. Troubleshoot non-compliant results.
• Assemble batch for review. Accurately enter patient results. Document all quality control values and submit data package to certification.
• Ensure balanced loading of instruments to maximize production.
• Maintain carrier gas stock; ensure adequate pressure and prevent instrument shutdown. • Actively monitor/search for priority SIDs/batches ensuring timely prep, workup, and release; prioritize work as needed.
• Maintain and protect the confidentiality of all CRL, CRL subsidiaries, legal entities and client information.
• Be able to comply with all applicable federal, state, and local safety and health regulations that would apply to this job.
Other duties as assigned.
JOB QUALIFICATIONS:
EDUCATION: A doctoral, master’s, or bachelor’s degree in medical technology, clinical laboratory, chemical, or biological science.
EXPERIENCE:
• High Complexity Testing:
Bachelor’s Degree or higher: training/experience as specified in 42CFR493.1489
Acting Technical Supervisor: Education: Bachelor’s degree in a chemical or biological or clinical laboratory science, or medical technology from an accredited institution or equivalent. Experience: 4 years of pertinent laboratory experience.
• Previous laboratory experience.
• Familiarity with sample preparation and/or LC/MS/MS preferred.
SKILLS & ABILITIES:
• Good verbal and written communication skills
• Strong organizational skills
• Ability to work under time constraints
• Detail oriented
• Good judgment and decision making skills
• Ability to follow instructions precisely
• Good laboratory technique
• Ability to be at work and on time
• Ability and judgment to interact and communicate appropriately with other employees, clients and management
PHYSICAL REQUIREMENTS: The physical demands described here are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be available to enable qualified individuals with disabilities to perform the essential functions.
The following physical attributes are required for this position:
• Sitting for extended lengths of time
• Regularly required to move around laboratory
• Close vision requirements due to computer work
• Repetitive use of hands, fingers, wrists, and elbows for operating a computer and telephone
• Reaching, including above the shoulder
• Bending or stooping
• Squatting or crouching
• Kneeling
• Climbing
• Lifting up to 25 pounds
EQUIPMENT: Must operate and maintain automated testing instrumentation. Automated pipettors, centrifuge; shaker/rotator; heating block; pH meter; analytical balance; various automated instruments; pipette; lab coat; gloves; gas cylinders; PC; LC/MS/MS.
OTHER: Overtime as necessary; weekend work is required; specimens consist of body fluids and must be regarded as potentially infectious; exposure to caustics, flammables, solvents, carcinogens, and reactive compounds.
The employer shall, in its discretion, modify or adjust this position to meet the company’s changing needs.
This job description is not a contract and may be adjusted as deemed appropriate in the employer’s sole discretion.
• denotes essential job function
An Equal Opportunity Employer
Pay Range: $23.00 - $41.00
Benefits for Full Time Employees:
CRL was originally founded as Enzyme Technologies in 1979 with our focus on clinical research and development. The name was changed to Clinical Reference Laboratory in 1983 when we began to offer commercial lab testing. Today, CRL has become one of the largest privately held clinical testing laboratories in the U.S., performing hundreds of thousands of tests every day for clients large and small. Our staff works around-the-clock to process and report results seven days a week.
We are driven each day to provide the useful insights people need to live healthy, safe, and productive lives. We serve insurers, employers, healthcare providers and their patients, colleges and universities, as well as federal, state, and local government agencies through a broad array of corporate and personal wellness programs, drugs of abuse testing programs, insurance risk assessment, and molecular diagnostics testing.
Together with FormFox, the nation’s leading provider of ECCF and electronic workflow solutions, we provide integrated solutions for workplace drugs of abuse testing, occupational health testing, and clinical lab testing services. CRL’s industry-leading turnaround times and state-of-the-art equipment and technology, paired with FormFox’s data management and digital workflow solutions, seamlessly connect all participants.
Our mission isn’t to be the most recognized lab, but to be the most trusted laboratory partner by providing personalized service, accurate testing, rapid turnaround time, and innovative systems and solutions. We conduct research, advance our test menu, pursue collaborations, discover new applications for existing data, and hold ourselves to the highest level of quality and client support standards, uniquely positioning our partners to achieve the best possible outcomes. And we do it all with a human touch.
