Number of Job Openings Available:

1

Date Posted:

December 18, 2024

Department:

72006344 Central Lab Cytogenetics

Shift:

Day (United States of America)

Shift Length:

8 hour shift

Hours Per Week:

40

Union Contract:

SEIU-9-Central Lab

Weekend Rotation:

Every 3rd

Job Summary:

Allina Health is a not-for-profit health system that cares for individuals, families and communities throughout Minnesota and western Wisconsin. If you value putting patients first, consider a career at Allina Health. Our mission is to provide exceptional care as we prevent illness, restore health and provide comfort to all who entrust us with their care. This includes you and your loved ones. We are committed to providing whole person care, investing in your well-being, and enriching your career.

Key Position Details:

Full time position8-hour, day shiftsEvery third weekend rotationSEIU represented position

Job Description:

Performs high complexity testing in the cytogenetics specialty of the pathology department. This includes the accurate and timely processing of specimens, and performing routine and complex laboratory procedures with strict adherence to quality control and quality assurance policies. May serve as a key operator for a technical work area, including oversight of regulatory compliance, new method validation, technical procedures, and inventory control.

CLIA Role:
Testing Personnel
Moderate complexity testing

Testing Personnel
High Complexity testing.

Principle Responsibilities

Performs routine and complex laboratory procedures.Performs analytical tests.Prepares specimens for culture, harvest, slide preparation and staining, FISH processing, and analysis.Performs cytogenetic analysis, including analysis of digital images and microscopic analysis, and documents results.Correlates analysis results with patient’s reason-for-referral, previous studies, related family studies as applicable and additional pathology/test results as available.Evaluates results for accuracy, and resolves complex test problems.Recognizes, communicates, and documents results that require action.Follows all federal regulations including CAP, OSHA, COLA, CLIA, ACMG and HIPAA.Performs and documents required & advanced instrument maintenance, and quality control.Performs and documents required reagent preparation.Performs quality control, and takes appropriate remedial action.Ensures appropriate documentation and record retention according to federal regulations.Performs proficiency testing as assigned.Processes Specimen.Performs all aspects of specimen management, including confirmation of patient identity and labeling of specimens and aliquots.Coordinates and performs the processing of cytogenetic specimens.Assesses all pre-analytic processes and documents all sub-optimal situations.Evaluates patient orders for completeness and follows up as needed.Maintains safety, education, and competency requirements.Stocks, rotates and requests supplies on a regular basis to ensure proper availability in the work area.Participates in the training of new employees and students.Assists in Direct Observation of staff for annual competency.Participates in development of technical procedures, forms, miscellaneous documents, method validation, and implementation.Participates in departmental or system meetings, projects and committees as assigned.May assist with department scheduling.Performs proficiency testing as assigned.CLIA defined responsibilities:§ 493.1425 Standard; Testing personnel responsibilities. Moderate complexity.§ 493.1495 Standard; Testing personnel responsibilities.Other duties as assigned.

Required Qualifications

Bachelor's degree from an accredited college/universityANDsuccessful completion of a NAACLS accredited cytogenetics education program within the last five years orBachelor's degree from a regionally accredited college/university with a major in biological science or chemistry, or a bachelor's degree including 30 semester hours (45 quarter hours) of college course work in the biological, chemical and/or medical sciences from a regionally accredited college/universityANDone year of full-time acceptable work experience in a clinical cytogenetics laboratory in the U.S., Canada or an accredited laboratory within the last three years orMaster's degree or Doctorate in genetics or molecular biology from a regionally accredited college/universityANDnine months of full-time acceptable work experience in a clinical cytogenetics laboratory in the U.S., Canada, or an accredited laboratory within the last three yearsCLIA defined Qualifications: § 493.1423 Standard; Testing personnel qualificationsCLIA defined Qualifications: § 493.1489 Standard; Testing personnel qualificationsCLIA defined Qualifications: § 493.1491 Technologist qualifications on or before February 28, 1992

Licenses/Certifications

Technologist in Cytogenetics CG (ASCP) within 6 months required

Physical Demands

Light Work:Lifting weight Up to 20 lbs. occasionally, Up to 10 lbs. frequently