- Responsible for leading and coordinating Regulated maintenance activities within Equipment Maintenance Department (EMD), USAMRIID to ensure maintenance documentation for laboratory instrumentation is qualified to comply with regulatory requirements. This person will be responsible for tracking of equipment used in all Regulated (once referred to only as GLP) studies, development and recommendation of maintenance intervals, coordination of due dates, maintenance procedures, as well as management of related maintenance documentation. In addition, this person will be responsible for tracking the submission and completion of work request submitted to EMD for the repair of malfunctioning laboratory equipment necessary to maintain critical workflow in support of Regulated Studies.
- Scheduling Services. Responsible for coordinating routine and unscheduled maintenance services on a variety of complex laboratory instrumentation. This task involves coordination through the equipment user or laboratory supervisor to ensure the availability of equipment and possible decontamination of equipment prior to the service being performed. For services performed by personnel outside of internal maintenance personnel, arrangements must be made with approved qualified personnel to have the service performed.
- Hand Receipt Management. Provide as needed assistance in tracking and management of nonexpendable equipment used in Regulated studies. This includes maintaining accurate hand receipt documentation, interfacing with the equipment custodian or the Study Director and updating hand receipt information in DMLSS.
- Purchase Request Submission. Assist internal customers with technical assistance in researching vendors and sources for medical device/medical device system equipment and service-related purchase request to meet critical timelines and suspense's.
- Document Review. Review and facilitate all Regulated equipment maintenance checklist, all modalities of medical device/medical devices systems, (currently 115 Preventive maintenance and Calibration Service checklist on file) and SOP's requiring EMD actions and/or signatures. Ensure all documentation requirements are maintained and uploaded into DMLSS equipment record. Assist customers and QARCO staff in preparing documentation for validation procedures IAW the SOP.
- Possess the ability to communicate effectively with the COTR, both orally and in writing, and follow directions in detail with minimal supervision.
- The qualified candidate will also be required to review and provide input to all USAMRIID SOPs, Forms, and protocols that involve Regulated equipment or its maintenance.
- The qualified candidate will be required to attend Meetings, focus groups, and workgroups that pertain to Regulated equipment and studies and provide input to ensure valid outcomes as well as reports to management when requested. If updates or changes are required it will be presented to BMET staff for implementation. Bi-weekly at CEB shop meeting.
- The qualified candidate will be required to track validation protocols and change controls that pertain to equipment records and work requests and query maintenance management system to provide reports as needed.
- May need to work additional hours to support taskers or operations orders that may temporarily increase workload.
- Perform other related duties, as assigned or required.
- Experience as a lead, scheduling work, and/or overseeing and mentoring technical work of others
- Experience performing biomedical equipment maintenance, repair, and maintenance cycles on Military Medical Equipment.
- Experience performing complex technical inspections of new, used or reconditioned Army medical equipment.
- Experience with medical equipment overhaul.
- Proven technical writing skills.
- Experience with MS Office Suite
- Defense Medical Logistics Standard Support (DMLSS) Experience
- Excellent time management skills
- Excellent verbal and written communication skills
- Bachelor's Degree or equivalent years of experience.
- Minimum f
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Biomedical Equipment Repair - Fort Detrick, United States - Goldbelt Incorporated
Description
Overview
Goldbelt Frontier is committed to providing support for a range of health technology management operations, projects, and services across the government and commercial industries.
Frontier collaborates with clients and partners with other businesses to ensure that the right solution with the right people is delivered to meet the client's needs.
Many senior project managers and business analysts are subject matter experts in their respective fields. Frontier understands how to support multiple stakeholders to aid in developing and implementing national policies, strategies, and doctrine.Summary:
A Biomedical Equipment Technician (BMET) uses traditional engineering expertise to analyze and solve problems regarding the design, development, and safety testing of biomedical equipment.
They serve as the principal action officer for maintenance related acquisition support, fielding, and sustainment of medical laboratory equipment, contact patient monitoring systems, and digital imaging/radiographic equipment.
May provide leadership and/or supervisory oversight to other BMETs.Responsibilities
Essential Job Functions:
Necessary Skills and Knowledge:
Minimum Qualifications: