- Compass Group, North America (Chicago, IL)
- …initiatives across assigned hospital accounts. This role focuses on medical device integration, project execution, and capital equipment coordination to support ... RESPONSIBILITIES + Project Leadership: Plan, coordinate, and oversee medical device integration projects, ensuring timely completion, stakeholder communication, and… more
- Cleveland Clinic (Weston, FL)
- …and without magnet application (pacemaker only). + Perform interrogation of the patient's device with the programmer that is appropriate for their device , ... the pacemaker lead(s) to determine optimal settings for the device . + Determine underlying rhythm and sensing function, if...and provide booklets for patient education. + Note any device and lead alerts that are received from any… more
- Veterans Affairs, Veterans Health Administration (Grand Island, NE)
- …with providers and allied health colleagues regarding treatment. Ability to assess device to ensure structural soundness and compliance with prescription and fit. ... KSAs: Skill in developing a follow up treatment plan for complex pedorthic device types. Ability to process paperwork for pedorthic devices being produced and fitted… more
- Integra LifeSciences (Plainsboro, NJ)
- …US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device Regulations (CMDR), and other ... Food and Drug Administration (FDA) regulations, ISO 9001, ISO 13485:2003, Medical Device Directive (MOD), the Canadian Medical Device Regulations (CMDR), Integra… more
- GE HealthCare (Cleveland, OH)
- …either Medical Devices or Pharmaceuticals, preferably with Software as a Medical Device (SaMD) Demonstrated understanding of Medical Device Quality Management ... in Quality Assurance or Quality Engineering within the Medical Device or Pharmaceutical industry, or in Design Engineering in...in Design Engineering in the Software as a Medical Device field (SaMD). + Demonstrated expertise in Medical … more
- Abbott (Plymouth, MN)
- …In this role, you will also be responsible for performing medical device regulatory reporting in accordance with global regulatory guidelines, ensuring timely and ... You'll Work On** + Independently determining and filing appropriate medical device regulatory reports with various regulatory agencies and worldwide governing… more
- Actalent (Salt Lake City, UT)
- …an experienced Electrical/Electronic Engineer to provide technical expertise and ensure device design concepts adhere to sound engineering principles using the ... across teams to deliver innovative and reliable solutions for device development. Responsibilities: + Apply electrical/electronic engineering principles to develop… more
- Medtronic (Jacksonville, FL)
- …integration and compliance. + Develop and review documentation according to medical device regulatory standards (eg, IEC 62304). + Conduct code reviews, unit ... with C and C++. + Developed and reviewed documentation according to medical device regulatory standards (eg, IEC 62304). + Proven track record of leading software… more
- Stryker (Houston, TX)
- …in increased clinical acumen. Responsibilities: + Educate physicians on device handling, implantation and troubleshooting techniques related to Inari products. ... Collaborate with product development teams to provide feedback on device features and new device development +...provide feedback on device features and new device development + Document procedural case observations for regulatory… more
- Stryker (Redmond, WA)
- …play a critical role in supporting our regulated Class III medical device products by driving excellence in build automation and continuous integration. You'll ... bug tracking tools. + Create efficient deployment processes for medical device software and ensure compliance with industry standards and regulatory requirements.… more