Scientist III

ARUP Laboratories Career•Salt Lake City, UT

21h•Onsite

About The Position

This position is a mid-level staff scientific position and functions with a proportionally reduced amount of formal direction and commensurate autonomy. Works under the oversight of the Medical Directorship and reports directly to the R&D Manager. ARUP Laboratories is a national clinical and anatomic pathology reference laboratory and an enterprise of the University of Utah and its Department of Pathology. Based in Salt Lake City, Utah. ARUP proudly hires top talent to create a work environment of diversity, professional growth and continuous development. Our workforce is committed to the important service we אנחנו provide to over one million patients each month. We always strive for excellence and have a strong desire to have involvement with the advances in medicine and the role laboratory services plays within each patient’s life. We never forget that there is a patient behind every specimen we receive. We are looking for individuals who want to contribute to ARUP's culture of accountability, integrity, service, and excellence. Consider joining our dynamic team.

Requirements

Mid-level staff scientific position.
Functions with a proportionally reduced amount of formal direction and commensurate autonomy.
Works under the oversight of the Medical Directorship.
Reports directly to the R&D Manager.
Stooping: Bending body downward and forward by bending spine at the waist.
Reaching: Extending hand(s) and arm(s) in any direction.
Mobility: The person in this position needs to occasionally move between work sites and inside the office to access file cabinets, office machinery, etc.
PPE: Biohazard laboratory environment that requires use of personal protective equipment in accordance with CDC and OSHA regulations and company policies.
To conduct self in compliance with all ARUP Policies and Procedures.
Sedentary Work: Exerting up to 10 pounds of force occasionally and/or negligible amount of force frequently or constantly to lift, carry, push, pull or otherwise move objects.
Fine Motor Control: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling.
Vision: Having close, far, and peripheral visual acuity to perform a variety of tasks such as make general observations of depth and distance.

Nice To Haves

Experience with mass spectrometry based bioanalytical assays is strongly preferred, including biological sample preparation and GC/LC separations.

Responsibilities

Researches, organizes and implements new assays and methodologies as well as improves current testing.
Writes technical procedures for transition into the clinical lab.
Oversees, designs, and executes all aspects of development and validation/verification of new assays or assay improvements for the technical section.
Performs literature reviews to access breadth of field(s) to inform new assay development and assay improvement.
Maintains knowledge of field and awareness of new and emerging technologies and their potential applications to the reference setting.
Writes comprehensive analytical protocols, development plans, and validation/verification plans.
Ensures protocols are in compliance with department, company, and appropriate regulatory body’s regulations.
Critically evaluates and interprets experimental data.
Works within corporate guidelines to record, archive, and report all data.
Compiles data and reports into Validation/Verification packets per ARUP R&D policies.
Appropriately prioritizes projects and tasks and demonstrates effective skill in time management.
Communicates regularly with Medical Directors, R&D Manager, and Technical Operations to relay project progress, experimental results, and data analysis.
Works with Technical Operations management and staff to implement new assays or assay improvements including but not limited to training technical staff in assay execution following validation and monitoring assay performance following “Go Live”.
Provides laboratory support for validation of new equipment, processes, and methods.
Works with Technical Operations management and staff to effectively troubleshoot issues with new and existing assays.
Works effectively with all ARUP departments to ensure all facets of Validation/Verification process are addressed and assays are successfully launched.
Presents data and results in regular lab meetings, ARUP seminars, and professional meetings and conferences when required.
Consolidates data, results, and conclusions and prepares manuscripts for publication in peer reviewed journals when required.
Other duties as assigned.