Technical Specialist Visa Sponsorship Jobs in Texas

INTRODUCTION

We are searching for a Technical Specialist – someone who works well in a fast-paced setting. In 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.

QUALIFICATIONS

• Bachelor’s degree in clinical laboratory science, chemical, physical, or biological science required
• Master’s 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 student’s performance
• Performs other essential job-related functions assigned by the supervisor and/or leadership team