Biomedical Engineer (BMET)

RBCI•Frederick, MD

9d•Hybrid

About The Position

RBCI is seeking a Biomedical Equipment Technician/Specialist (BMET/S) to support our DoD customer. This role will involve supporting the advanced development and fielding of military medical equipment, as well as participating in programs that oversee lifecycle maintenance and implementation. The position is located at Fort Detrick, MD, with a hybrid work arrangement. Military Veterans are highly encouraged to apply.

Requirements

Bachelor's Degree in related field with 4 years related experience; or a minimum of 7 years related experience in lieu of a degree.
Must be a U.S. Citizen.
Ability to obtain NACI (background investigation) clearance.
Seven (7) years of experience with medical product development, DoD T&E requirements, and regulatory approval processes.
Familiarity and experience with pharmacy equipment including medical cabinets, pill dispensers, medication dispensing systems, unit dose packing system.
Prepare and deliver documents ranging from technical reviews to acquisition documentation.

Nice To Haves

Military Veterans are highly encouraged to apply.

Responsibilities

Support evaluation of Biomedical Equipment (POD)
Analyze medical equipment using maintenance data, usage and life cycle data, and technology standards.
Provide input and written reports, evaluations, and recommendations for fixed facility hospitals on their standard of care.
Ensure that the biomedical equipment is in compliance with applicable regulatory requirements and quality control standards.
Create and evaluate Systems Requirements Documents (SRD's) for purchase criteria within each Request for Offer package (RFO).
Evaluate RFO packages conducting down selections for equipment purchases through the Defense Logistics Agency (DLA).
Assist with design, help develop and provide safety testing, repair, and maintenance of biomedical equipment.
Support PMO operations.
Participate and actively engage on Integrated Product Teams (IPT) and Working Groups (WG) as a Chartered Member and serve as the technical expert by providing expert advice.
Prepare and deliver documents ranging from technical reviews to acquisition documentation.
Conduct market analysis to include available products and industries, gain an understanding of product market survivability and viability as a crucial component for the execution of force-wide fielding.
Review test plans, and results and reports from clinical studies and other testing, to include the review of the final study reports at the end of each phase of a clinical study, and/or lab results from testing facilities.
Assist the PdM's in review of regular Program Objective Memorandum (POM) cycles, spend plans, cost estimating and other cost analysis requirements.
Monitor, track and report on program cost, schedule and performance.