Technical Specialist - Digital Pathology
Technical Specialist - Digital Pathology
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Job Description
We are searching for a Technical Specialist someone who works well in a fast-paced this position you will oversee workflow and perform quality assurance duties in the laboratory section of your responsibility. You may also serve as team leader scheduler and primary trainer for the section.
Think youve got what it takes
Qualifications:
Bachelors degree in clinical laboratory science chemical physical or biological science required
Masters degree (or higher) in biological chemistry or laboratory science may substitute for one year of the required experience
BB-ASCP C-ASP CLSP-NCA G-ASCP HT-ASCP HTL-ASCP M-ASCP MB-ASCP MLS-ASCP MP-ASCP MT-AMT MT-ASCP MT-NCA or MT-STATE certification preferred
One of the above certifications may substitute for one year of the required experience
3 years experience in a laboratory setting applicable to their area of responsibility required
Responsibilities:
Assists with all NGS validations studies and other projects in collaboration with technical and professional staff and other personnel as negotiated by Medical Director; collaborates with medical director as appropriate in applied research and publications
Assists with the development of processes/written procedures required for the implementation of new or modified testing and quality program essentials
Assists other employees in troubleshooting specimen problems errors and performance of workload in order to meet established turnaround times.
Assists with the review of daily and monthly quality control reports communicates with supervisor in a timely manner about any quality control problems and follows with corrective action as needed.
Maintains appropriate inventory levels and orders supplies; monitors reagent crossover checks and expiration dates.
Acts as lead trainer in section helps create training materials and assessment tools; oversees and performs annual competency observations.
Assists with the performance of proficiency studies and surveys ensuring that materials are processed tested and reported accurately; investigates problems or unacceptable results and assist with completion of necessary documentation
Assist Supervisor with maintenance of QA/QI program monitors safety practices and compliance in work area assists with CAP compliance and inspections
Troubleshoots LIS orders as they occur interface applications and system upgrades and participates in LIS user group meetings for new test development
Acts as lead coordinator for the medical technology internship programs. Reviews training materials and checklists. Schedules training assignments and evaluates students performance.
Performs other essential job-related functions assigned by the supervisor and/or leadership team
Required Experience:
Unclear Seniority
Employment Type
Full-Time
