Technical Lead, Laboratory, Molecular Diagonostic - Day Shift

Company:  The University of Chicago Medicine
Location: Chicago
Closing Date: 23/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Job Description:
Be a part of a world-class academic healthcare system, UChicago Medicine, as a Technical Lead in the Molecular Diagostics department. Here, you will conduct a wide variety of inherited and somatic molecular procedures to detect diseases and support pharmacogenomic treatment protocols.  Responsible for quality control, instrument maintenance, and method development to support a broad menu of tests to support targeted treatment modalities and monitor the patient’s prognosis.  Works collaboratively with colleagues, participates in process improvement projects, and trains MT students.  This department is the Molecular Diagostics Laboratory. This position is a 100% onsite opportunity. You will need to be based in the greater Chicagoland area.

 

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, assuming a leadership role in the process of continuous quality improvement, 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. Ability to perform a wide range of clinical analyses in all sections of the laboratory by properly utilizing a variety of methodologies and instrumentation according to laboratory policies and procedures and in accordance with all regulatory agency requirements in order to provide results of the highest level of quality to physicians and our patients.

 

Essential Job Functions

Serves as a subject matter expert within specific laboratory department 

Acts as lead in the development, evaluation, validation, and implementation of new clinical laboratory procedures, equipment, and processes

Completes assigned projects and tasks in a timely manner with little or no supervision and engages the team in projects

Identifies laboratory and clinical needs related to area of subspecialty expertise including projects, initiatives, quality assurance, and compliance

Provide guidance to testing personnel performing moderate and high complexity testing

Acts as knowledgeable leader to assist Medical Laboratory Scientist and Technicians

Resolves technical problems, performs advanced troubleshooting, provides thorough assessment on technical issues and decisions, and evaluate external assistance when necessary

Reports all test results in the laboratory information system according to laboratory policies and procedures, within stated turn-around times, and follows appropriate backup procedures during computer downtimes

Practices the proficient and safe use of all equipment necessary for the completion of all duties and responsibilities by following all maintenance, operation, safety and quality controls policies and procedures

Demonstrates knowledge of techniques, principles, and instruments and their interrelationships as well as physiological conditions affecting test results

Analyzes all test and quality controls and reviews for errors, inconsistencies and deviations prior to reporting results

Initiates, documents, troubleshoot to ensure remedial actions are taken whenever test systems/QA deviate from established performance specifications

Communicates information or problems with laboratory team and leadership in a respectful and proactive manner

Contributes in maintaining continual compliance with policies, procedures and record keeping necessary to meet standards of accrediting or regulatory agencies

Participates in the quality management program including quality control review, annual procedure review, compliance requirements, quality improvement, and implementation of the training and competency program

Participate in educational and training activities to acquire new skills, maintain technical relevance and improve proficiency

Provides patient-focused care in a clinical setting through the accurate performance of routine and complex tests through the pre-analytic, analytic and post-analytic stages

Answers inquiries regarding specimen handling, results and other technical information

Appropriately assists clinicians with requests and seeks out resources necessary when information is not available to answer questions

Effectively communicates all pertinent information with appropriate laboratory staff and lab leadership

Acts in a consistently professional manner while conducting all duties and responsibilities 

Ability to recognize strengths and weaknesses in themselves and others, can adapt to change, and remain professional in stressful situations

Required Qualifications

Must satisfy CLIA 88 qualification requirements for general supervisor who oversees testing personnel performing 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 American Society of Clinical Pathologists (ASCP) or equivalent

Knowledge and ability to use laboratory and hospitals information systems 

Ability to use and understand basic statistical concepts and methods that are commonly utilized in clinical laboratory science.  Proficiency in laboratory data analytics 

Ability to interact in a professional manner with individuals at all levels 

Exceptional organizational skills, ability to work in stress situations, and pay attention to details

Preferred Qualifications 

Three years of Molecular Genomics experience performing Next Generation Sequencing

Test development experience (assay development and validation experience)

Position Details 

Job Type/FTE: Fulltime (1.0)

Shift:  Day Shift (8:00 am - 4:30 pm)

Work Location: Hyde Park

Unit/Department:  Molecular Diagonostic 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, an individual. To accomplish this, we need employees with passion, talent and commitment… with patients and with each other. We’re in this together: working to advance medical innovation, serve the health needs of the community, and move our collective knowledge forward. If you’d like to add enriching human life to your profile, UChicago Medicine is for you. Here at the forefront, we’re doing work that really matters. Join us. Bring your passion.

 

UChicago Medicine is growing; discover how you can be a part of this pursuit of excellence at: .

 

UChicago Medicine is an equal opportunity employer.  We evaluate qualified applicants without regard to race, color, ethnicity, ancestry, sex, sexual orientation, gender identity, marital status, civil union status, parental status, religion, national origin, age, disability, veteran status and other legally protected characteristics.

 

Must comply with UChicago Medicine’s COVID-19 Vaccination requirement as a condition of employment. If you have already received the vaccination, you must provide proof as part of the pre-employment process. This is in addition to your compliance with the Flu Vaccination requirement as well. Medical and religious exemptions will be considered consistent with applicable law. Lastly, a pre-employment physical, drug screening, and background check are also required for all employees prior to hire.

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