Technical Specialist

Versiti•Indianapolis, IN

13d

About The Position

Under the direction of DL Leadership, provides guidance on technical issues to staff, leads quality and project initiatives, assists with technical & equipment troubleshooting, manages the development and implementation of new tests and assists with analysis and interpretation of complex test results in support of DL Hematology (Hemostasis Reference Lab, Molecular Oncology Genetics Lab, and Platelet & Neutrophil Immunology Lab), DL Histocompatibility or DL Immunohematology labs. This position has developed and demonstrated a level of quality and technical competence that allows for completing work in a highly independent and efficient manner and handling of complex technical issues. Provides support to clinical and research customers, including a high level of customer service and consultation on complex cases and problems. Trains and assesses competence of staff members and educational guests. In conjunction with the entire Lab Team, performs interpretation of complex patient test results, including consultations with clients, as required.

Requirements

Bachelor's Degree in Medical Laboratory Science or one of the chemical, physical, or biological sciences from an accredited college or university required
Master's Degree from an accredited institution with a major in one of the chemical, physical or biological sciences in lieu of required degree
Four years (post degree) related clinical laboratory experience to include at least two years under a director at the doctoral level required
Histocompatibility: Three years of laboratory training or experience in human immunogenetics, human histocompatibility and/or human transplantation immunology under the supervision of a director and/or technical supervisor of an ASHI-accredited or an equivalent ARB approved laboratory required
Immunohematology: 4-6 years working in an Immunohematology Reference Laboratory or Transfusion Service required
Knowledge of good laboratory practices and quality systems required
Working knowledge of and experience with regulations related to CLIA (Clinical Laboratory Improvement Act), serologic and molecular testing, and quality assurance concepts/practices required
Experience serving as a subject matter expert (SME) to laboratory staff, other labs/departments, regulatory agencies, and/or external customers as needed required
Well developed skills in the planning, organizing and management of cross-functional teams with the ability to influence and motivate others in implementing process changes required
Strong detail orientation and analytical ability required
Effective oral and written communication skills required
Computer skills including word processing, electronic spreadsheets, and other database software programs required
Histocompatibility: Certified Histocompatibility Specialist (CHS) or Technologist (CHT) within 1 Year required
Immunohematology: MLS (ASCP) and SBB certifications or equivalents; within 1 Year required

Responsibilities

Assists with test selection, analysis, review, and interpretation for clinical and VCT patients.
Leads assay, sample, result, and equipment troubleshooting.
Performs testing on clinical and/or clinical/contract research samples as needed.
Performs management final review of result review and release.
Part of the management on-call rotation for results review and release (Histocompatibility and Immunohematology).
Serves as a technical resource and/or provides clinical consultation to laboratory staff, other labs/departments, and/or external customers as needed.
Trains and assesses competence of clinical diagnostic lab staff.
Provides orientation to testing personnel.
Assists in the creation of training materials for staff and students, as needed.
Monitors test analysis and specimen examinations to ensure that acceptable levels of analytic performance are maintained.
Assures that all remedial actions are taken when test systems deviate from the laboratory’s established performance specifications.
Ensures that patient test results are not reported until all corrective actions have been taken and the test system is properly functioning.
Serves as an internal resource regarding quality testing and reporting regarding the requirements of CAP (College of American Pathology), AABB, FDA and CLIA regulations as applicable to the lab.
With lab leadership, promotes and maintains compliance of lab operations with all applicable policies, standards, and regulations.
Assists with operating within the Quality Management System (QMS), including all systems that support the QMS.
Provides support during internal and external audits/assessments as needed.
Responsible for management of specific projects, such as test enhancements, continuous improvement projects, or new equipment implementations; evaluates needs, plans, facilitates, delegates, and/or performs tasks ensuring project completion within designated timeframes.
Remains current and knowledgeable on trends in lab practices, relevant regulations, and business climate.
Stays abreast of latest technology and trends in diagnostic testing and looks for innovative product and service ideas to serve more patients in new or better ways.
Accountable for equipment, technology, reagent, and software improvements and/or implementations working with internal and external resources to serve more patients in new or better ways.
Accessible to testing personnel at all time testing is performed providing on-site, telephone, or electronic consultation, providing day-to-day supervision of High complexity test performance.
Evaluates, qualifies, and recommends suppliers for equipment, software, and/or reagent purchasing.
Collaborates with other laboratories for supplier leverage.
Performs cost analysis of current tests and procedures.
Partners with the leadership team in areas of technology, compliance, customer service, and process control.
Establishes educational partnerships with local educational institutions to increase Versiti visibility and to enhance recruitment potential.
Attends and presents at relevant local, national, and international meetings.
Serves as technical and clinical education resource and liaison for potential, new, and existing customers.
May provide scientific support to Business Development team.
Performs other duties as required or assigned which are reasonably within the scope of the duties in this job classification.
Understands and performs in accordance with all applicable regulatory and compliance requirements.
Complies with all standard operating policies and procedures.