Group Lead, Med Lab Scientist

Simple Laboratories•Chicago, IL

2d•Onsite

About The Position

Simple Laboratories is looking for a Group Lead, Medical Laboratory Scientist, ASCP/AMT licensed individual who performs test procedures of moderate/high complexity at our Humboldt Park, Chicago laboratory location. The Group Lead, MLS is expected to demonstrate competency in all assays/instrument's cross sections [Generalist] including Blood Bank. Additionally, reporting to the Lab Manager providing team oversight and guidance as needed and serving as a technical resource for the department. Shift Schedule: 8:00 AM to 3:30 PM with alternating weekends

Requirements

Bachelor’s degree in Chemistry, Biology, Clinical Laboratory Sciences, or Medical Technology program from an accredited institution required.
MLS/MT (ASCP), AMT or another national accreditation required.
Meets CLIA requirements for high complexity testing personnel.
Comprehensive theoretical and operational job knowledge in designated specialty discipline.
Proven leadership and problem-solving skills.
Must be detail-oriented, can work independently, establish work priorities for self and other team members, to handle several tasks simultaneously for maximum laboratory efficiency.
Ability to schedule and manage resources to meet department goals.
Strong interpersonal skills to facilitate collaborative and cohesive relationships with internal and external customers and stakeholders.
Strong communication skills are necessary to handle inquiries from internal and external customers, both verbal and written.
Ability to deal with client information in a confidential manner.
Proficiency in Microsoft Office (Word, Excel, Outlook, Teams) and company LIS.

Nice To Haves

Demonstrate competency in all assays/instrument's cross sections [Generalist] including Blood Bank.

Responsibilities

Demonstrate full proficiency in all duties of a Medical Lab Scientist
Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met.
Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results.
Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients.
Perform, review and document QC analysis to ensure accuracy of clinical data and proper instrument function. Make quality control decisions regarding the disposition of an assay or test.
Review requests for validity checks and recommend an appropriate course of action in consideration of the limitations of specimen requirements and the effects of time and the quality of additional and/or repeat testing.
Serve as a technical resource for the department by investigating and resolving analytical testing problems, recommending a course of action in instances identified as beyond acceptable limits, and responding to non-routine/complex inquiries and/or requests from clients and Business Development team.
Assist Lab Manager by monitoring workflow to meet testing schedules; distributing and reviewing work assignments; training employees in laboratory techniques; resolving work-related problems of staff; and providing input for performance appraisals and disciplinary actions.
Expedite the flow of work to maximize productive capacity by evaluating production systems and recommending enhancements and coordinating the resolution of production problems/issues involving other laboratory departments.
Maintain laboratory areas and equipment in a safe, functional and sanitary condition.
Complete training and competency checklists as appropriate and assist with the department’s annual competency testing process and documentation.
Adheres to all established CLIA, HIPAA, OSHA, and laboratory safety requirements and reviews department activities to ensure compliance.
Participate in government or regulatory agency inspections, as needed.