Advance Development Lead

NEW HAVEN, CT
Sep 23, 2020

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Job Description

Overview

To be part of our organization, every employee should understand and share in the YNHHS Vision, support our Mission, and live our Values. These values - integrity, patient-centered, respect, accountability, and compassion - must guide what we do, as individuals and professionals, every day.

Under the supervision of the Advanced Development Director, and reporting to the Manager of Molecular Pathology, the Advanced Development Lead Technologist will assist with the design, optimization and validation of clinical laboratory assays and new technology in accordance with CAP and CLIA guidelines. Responsibilities include experimental design, preparation of validation plans, SOP's and training documents. The Lead Technologist will work closely with the Laboratory Manager and supervisors to transfer assays/technology from development to clinical production. Additional responsibilities include quality review of assays post-implementation and the optimization of current assays.

EEO/AA/Disability/Veteran

Responsibilities

  • 1. Performs and oversees development of new assays and technology following CAP and CLIA regulatory requirements.
  • 2. Understands and is able to apply basic principles of Molecular Diagnostics, laboratory procedure, theory, and techniques; understands instrumentation and equipment and shows good judgment in using them.
  • 3. Works with the Advanced Development Director, Laboratory Manager and Laboratory Section Directors to identify new assays and new technologies.
  • 4. Writes validation summaries, SOP's and training documents according to all regulatory guidelines.
  • 5. Assigns priorities to clinical and assay development responsibilities to ensure new assays are implemented in a timely fashion.
  • 6. Demonstrates a thorough knowledge of Quality Control data assessment; documents QC and corrective actions.
  • 7. Monitors quality and performs optimizations as needed of assays post-implementation.
  • 8. Actively participates in regulatory readiness for preparations.
  • 9. Provides accurate information to other team members and clinical staff as requested in an organized, courteous manner, and in a timely fashion.
  • 10. Able to navigate and show competency with the use of LIS applications. Can utilize the LIS to identify and track validation specimens effectively.
  • 11. Works with the LIS and clinical staff to design and test new assay test builds.
  • 12. Is proficient in data analysis software programs such as excel and EP Evaluator.
  • 13. Demonstrates self-reliance in one's thinking and action. Demonstrates independence by one's ability to evaluate culture integrity, problem solving, or trouble shooting instrumentation.
  • 14. Assumes the role of first line troubleshooter in areas of special expertise to answer routine and complex problems. Recognizes problems related to inappropriate outcome of procedures, takes corrective action when indicated.
  • 15. Is able to troubleshoot issues related assay design, instrumentation or software. Able to foster a team approach to solve problems with other departments within Laboratory Medicine by cultivating an atmosphere of mutual respect.
  • 16. Demonstrates professionalism at all times both in attitude and approach to work activities.
  • 17. Demonstrates a positive approach to learning new or existing methods, techniques and/or procedures. Accepts constructive criticism in a positive manner and takes corrective action to improve performance in problem areas.
  • 18. Participates in teaching lab personnel, students and lab residents following established laboratory procedures in a courteous professional manner. Always maintains a positive, respectful relationship with learner.
  • 19. Participates in the department's continuing education program and documents at least 12 education credits annually. Independently researches and suggests new methods and technology.
  • 20. Adheres to laboratory policies and procedures, hospital attendance and tardiness policies, and demonstration of mutual respect for all laboratory personnel.

Qualifications

EDUCATION


Bachelor's degree from an accredited university or college in a Biological Science or Biotechnology, Biochemistry, Molecular Biology, Microbiology, or equivalent Bachelor's degree. Advanced degree in Biological Sciences strongly preferred.


EXPERIENCE


Minimum of five (5) years clinical or research laboratory experience in a Molecular Diagnostics and/or Microbiology laboratory. Previous experience in assay design/development preferred. Experience in a CLIA certified laboratory preferred.


LICENSURE


ASCP certification preferred but not required.


SPECIAL SKILLS


Strong knowledge of molecular principles and techniques. Ability to design and execute experiments. Efficiency in word processing applications, spreadsheet design and data analysis. Excellent customer service and interpersonal skills are required. Ability to work as a member of a diverse team is essential. Excellent organizational skills required.


PHYSICAL DEMAND


Must be able to lift and carry 15 or more pounds.


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Job Info

Job: 22718

Department: Molecular Pathology
Category: TECHNOLOGIST/TECH
Sub Category: MEDICAL TECHNOLOGIST
Status: Full Time Benefits Eligible
Shift: DAYS
Hours: 40

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