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Lab Tech (Day Shift) (2083)

Job Description

The Laboratory Technician I is responsible for specimen processing, testing and monitoring test performance. The technician must demonstrate competency, as defined in the department’s training program, prior to performing independent testing. This position will work with department management and quality team members to ensure that laboratory activities are defined, documented and completed to support inspection readiness and that compliance is maintained through procedures, training, documentation and continuous improvement projects.
This is for a 4x10 shift Tuesday-Saturday, 8:00 AM to 6:30 PM

Responsibilities:
Each employee’s specific job responsibilities are uniquely defined by their individual training plan and assigned duties, but are generally defined as follows:

  1. Complying with the laboratory’s technical, administrative and safety policies and procedures.
  2. Participating in the laboratory’s quality assurance plan, adhering to quality control and preventive maintenance policies and appropriately documenting these activities.
  3. Following the laboratory’s policies and procedures whenever test systems are not within acceptable limits and documenting the problem and any corrective action.
  4. Troubleshooting and identifying problems that may adversely affect test performance and/or reporting of test results by initiating corrective action and using the defined electronic system to make the required management notification.
  5. Performing proficiency testing in the same manner as routine samples. 
  6. Actively participating in successful and timely completion of training and competency assessment as outlined in the laboratory and departmental training programs.
  7. Where competency has not been approved by supervision, will work under the direct supervision of an employee competent on the task.
  8. Participating in continuing education according to accepted laboratory standards.
  9. Participates within departmental team to resolve problems or implement projects.

Qualifications:
Supporting documentation for the education and experience requirements are maintained in the employee’s personnel file.

  1. Meets minimum regulatory education requirements:
  2. Doctorate (Ph.D., M.D. or D.O.) in medicine, clinical laboratory science, chemical, physical or biological science, or,
  3. Master’s degree in clinical laboratory science, chemical, physical or biological science, or,
  4. Bachelor’s degree in a chemical, physical, biological or clinical laboratory/medical technology science.
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About Us

Myriad Genetics Inc., is a leading personalized medicine company dedicated to being a trusted advisor transforming patient lives worldwide with pioneering molecular diagnostics. Myriad discovers and commercializes molecular diagnostic tests that: determine the risk of developing disease, accurately diagnose disease, assess the risk of disease progression, and guide treatment decisions across six major medical specialties where molecular diagnostics can significantly improve patient care and lower healthcare costs. Myriad is focused on three strategic imperatives: maintaining leadership in an expanding hereditary cancer market, diversifying its product portfolio through the introduction of new products and increasing the revenue contribution from international markets. For more information on how Myriad is making a difference, please visit the Company's website: www.myriad.com .

WE ARE AN EQUAL OPPORTUNITY EMPLOYER. Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, race, color, religion, gender,national origin, age, genetic information, military or veteran status, sexual orientation, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.

Please answer all questions completely. Please do not provide any information not specifically requested on this Employment Application form.




About the Team

Myriad Oncology, a business unit of Myriad Genetics focuses on three products EndoPredict®, BRACAnalysis CDx® and The Myriad myRisk® Hereditary Cancer. EndoPredict® can help accurately determine an individual patient’s 10-year risk of recurrence to help physicians identify which patients may consider safely forgoing chemotherapy.BRACAnalysis CDx® is an FDA-approved laboratory developed test for BRCA1 and BRCA2 intended to inform patient management related to the PARP inhibitors, Lynparza® (olaparib) and Zejula® (niraparib). The Myriad myRisk® Hereditary Cancer test is a multi-gene panel that identifies an elevated risk for eight hereditary cancers: Blending both genetic test status AND personal cancer family history, Myriad myRisk hereditary cancer panel represents the next generation of hereditary cancer risk testing.