UChicago Medicine
Technical Lead, Clinical Chemistry Laboratory Department - Days
UChicago Medicine, Chicago, Illinois, United States, 60290
Overview
Technical Lead, Clinical Chemistry Laboratory Department - Days at UChicago Medicine. Be part of a world-class academic healthcare system as a Technical Specialist in the Clinical Chemistry Department. Conduct a wide variety of technical procedures, operate a state-of-the-art integrated instrument system, and perform esoteric tests with current technology. Responsible for quality control, instrument maintenance, and method development to support a broad menu of routine chemistry, toxicology, endocrinology, immunochemistry, and therapeutic medications tests. Works collaboratively with colleagues, participates in process improvement projects, and trains MT students. This position is a 100% onsite opportunity in the greater Chicagoland area. Eligible for a sign-on bonus up to $10,000. In consultation with the Laboratory Manager, Laboratory Supervisor, and Medical Director, the Technical Lead serves as the primary specialist in a defined area of subspecialty expertise in the Clinical Laboratories. Responsibilities include development, implementation, evaluation and performance of tests, systems and procedures, staff training and competency, and participation in the laboratory accreditation cycle. Provides leadership in performing complex clinical pathology testing and instrument management of an advanced nature as defined for the specific clinical laboratory service. Responsibilities
Serve as a subject matter expert within a specific laboratory department Lead development, evaluation, validation, and implementation of new clinical laboratory procedures, equipment, and processes Complete assigned projects and tasks with minimal supervision and engage the team Identify laboratory and clinical needs related to the area of subspecialty expertise, including projects, initiatives, quality assurance, and compliance Provide guidance to testing personnel performing moderate and high complexity testing Act as a knowledgeable leader to assist Medical Laboratory Scientists and Technicians Resolve technical problems, perform advanced troubleshooting, assess technical issues, and evaluate external assistance when needed Report all test results in the laboratory information system per policies, within turnaround times, and follow backup procedures during downtimes Maintain safe and proficient use of equipment, following maintenance, operation, safety and quality control procedures Demonstrate knowledge of techniques, principles, and instruments and their interrelationships and how physiological conditions affect results Analyze test and quality control results, review for errors and deviations prior to reporting Initiate and document remedial actions when test systems/QA deviate from specifications Communicate information or problems with laboratory staff and leadership professionally Contribute to continual compliance with policies, procedures, and record keeping for accrediting/regulatory standards Participate in the quality management program, including quality control review, procedure reviews, compliance, quality improvement, and training/competency programs Participate in educational activities to acquire new skills and maintain technical relevance Provide patient-focused care through accurate performance of routine and complex tests across pre-analytic, analytic, and post-analytic stages Answer inquiries regarding specimen handling, results, and technical information Assist clinicians with requests and seek resources when information is unavailable Communicate pertinent information with laboratory staff and leadership Maintain a consistently professional approach in all duties Recognize strengths and weaknesses, adapt to change, and remain professional in stressful situations Required Qualifications
Must satisfy CLIA 88 qualification requirements for general supervisor overseeing high-complexity testing Bachelor's or advanced degree in clinical laboratory science or related field from an accredited college or university At least six years of prior work experience applicable to the specific technical discipline Certification or eligibility as Medical Laboratory Scientist (MLS) through ASCP or equivalent Knowledge and ability to use laboratory and hospital information systems Ability to use and understand basic statistical concepts and methods used in clinical laboratory science; proficiency in laboratory data analytics Ability to interact professionally with individuals at all levels Exceptional organizational skills and ability to work under stress with high attention to detail Preferred Qualifications
Certification in Chemistry (C) through ASCP Knowledge of clinical mass spectrometry-based systems and/or fully automated clinical chemistry systems Position Details
Job Type/FTE: Full-Time (1.0) Shift: Day Shift (8:00 am - 4:30 pm), Monday - Friday Work Location: Hyde Park Unit/Department: Clinical Chemistry Laboratory CBA Code: Non-Union Why Join Us
We’ve been at the forefront of medicine since 1899. We provide superior healthcare with compassion, always mindful that each patient is a person. We’re in this together: working to advance medical innovation, serve the health needs of the community, and move our collective knowledge forward. UChicago Medicine is an equal opportunity employer. All employees are required to complete a pre-employment physical, background check, drug screen, and comply with flu vaccination requirements prior to hire, with exemptions considered where allowed by law. Compensation & Benefits Overview: UChicago Medicine is committed to transparency in compensation and benefits. The pay range provided reflects the anticipated wage or salary for the position, and varies based on candidate qualifications and experience.
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Technical Lead, Clinical Chemistry Laboratory Department - Days at UChicago Medicine. Be part of a world-class academic healthcare system as a Technical Specialist in the Clinical Chemistry Department. Conduct a wide variety of technical procedures, operate a state-of-the-art integrated instrument system, and perform esoteric tests with current technology. Responsible for quality control, instrument maintenance, and method development to support a broad menu of routine chemistry, toxicology, endocrinology, immunochemistry, and therapeutic medications tests. Works collaboratively with colleagues, participates in process improvement projects, and trains MT students. This position is a 100% onsite opportunity in the greater Chicagoland area. Eligible for a sign-on bonus up to $10,000. In consultation with the Laboratory Manager, Laboratory Supervisor, and Medical Director, the Technical Lead serves as the primary specialist in a defined area of subspecialty expertise in the Clinical Laboratories. Responsibilities include development, implementation, evaluation and performance of tests, systems and procedures, staff training and competency, and participation in the laboratory accreditation cycle. Provides leadership in performing complex clinical pathology testing and instrument management of an advanced nature as defined for the specific clinical laboratory service. Responsibilities
Serve as a subject matter expert within a specific laboratory department Lead development, evaluation, validation, and implementation of new clinical laboratory procedures, equipment, and processes Complete assigned projects and tasks with minimal supervision and engage the team Identify laboratory and clinical needs related to the area of subspecialty expertise, including projects, initiatives, quality assurance, and compliance Provide guidance to testing personnel performing moderate and high complexity testing Act as a knowledgeable leader to assist Medical Laboratory Scientists and Technicians Resolve technical problems, perform advanced troubleshooting, assess technical issues, and evaluate external assistance when needed Report all test results in the laboratory information system per policies, within turnaround times, and follow backup procedures during downtimes Maintain safe and proficient use of equipment, following maintenance, operation, safety and quality control procedures Demonstrate knowledge of techniques, principles, and instruments and their interrelationships and how physiological conditions affect results Analyze test and quality control results, review for errors and deviations prior to reporting Initiate and document remedial actions when test systems/QA deviate from specifications Communicate information or problems with laboratory staff and leadership professionally Contribute to continual compliance with policies, procedures, and record keeping for accrediting/regulatory standards Participate in the quality management program, including quality control review, procedure reviews, compliance, quality improvement, and training/competency programs Participate in educational activities to acquire new skills and maintain technical relevance Provide patient-focused care through accurate performance of routine and complex tests across pre-analytic, analytic, and post-analytic stages Answer inquiries regarding specimen handling, results, and technical information Assist clinicians with requests and seek resources when information is unavailable Communicate pertinent information with laboratory staff and leadership Maintain a consistently professional approach in all duties Recognize strengths and weaknesses, adapt to change, and remain professional in stressful situations Required Qualifications
Must satisfy CLIA 88 qualification requirements for general supervisor overseeing high-complexity testing Bachelor's or advanced degree in clinical laboratory science or related field from an accredited college or university At least six years of prior work experience applicable to the specific technical discipline Certification or eligibility as Medical Laboratory Scientist (MLS) through ASCP or equivalent Knowledge and ability to use laboratory and hospital information systems Ability to use and understand basic statistical concepts and methods used in clinical laboratory science; proficiency in laboratory data analytics Ability to interact professionally with individuals at all levels Exceptional organizational skills and ability to work under stress with high attention to detail Preferred Qualifications
Certification in Chemistry (C) through ASCP Knowledge of clinical mass spectrometry-based systems and/or fully automated clinical chemistry systems Position Details
Job Type/FTE: Full-Time (1.0) Shift: Day Shift (8:00 am - 4:30 pm), Monday - Friday Work Location: Hyde Park Unit/Department: Clinical Chemistry Laboratory CBA Code: Non-Union Why Join Us
We’ve been at the forefront of medicine since 1899. We provide superior healthcare with compassion, always mindful that each patient is a person. We’re in this together: working to advance medical innovation, serve the health needs of the community, and move our collective knowledge forward. UChicago Medicine is an equal opportunity employer. All employees are required to complete a pre-employment physical, background check, drug screen, and comply with flu vaccination requirements prior to hire, with exemptions considered where allowed by law. Compensation & Benefits Overview: UChicago Medicine is committed to transparency in compensation and benefits. The pay range provided reflects the anticipated wage or salary for the position, and varies based on candidate qualifications and experience.
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