- Nissha Medical Technologies (Colorado Springs, CO)
- …analysis and Gauge R&R studies (preferred) + Experience working in a medical device manufacturing environment (preferred) + Experience authoring and executing ... and security rules set forth by the company and regulatory agencies **REQUIREMENTS:** + Bachelor's Degree in Engineering +... medical device process validation activities (preferred) +… more
- Integra LifeSciences (Plainsboro, NJ)
- … Medical Device Directive, the Canadian Medical Device Regulations (CMDR), and other applicable regulatory agencies. **Primary responsibilities are:** ... and guidelines: US Food and Drug Administration (FDA) regulations, ISO 9001, ISO 13485:2003, Medical Device Directive (MOD), the Canadian Medical Device … more
- Integra LifeSciences (Plainsboro, NJ)
- …13485, the Medical Device Directive, the Canadian Medical Device Regulations (CMDR), and other applicable regulatory agencies. The QA Engineer II ... and guidelines: US Food and Drug Administration (FDA) regulations, ISO 9001, ISO 13485, Medical Device Directive (MOD), the Canadian Medical Device … more
- Abbott (Beaverton, OR)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... applications + Must have excellent oral and written communication skills. **Preferred** + Medical Device experience strongly preferred. + Experience in an agile… more
- Abbott (Pleasanton, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... experienced **_Staff Engineer, Software Design Quality_** to ensure our medical devices are developed in accordance with...ISO 13485, ISO 14971, Software Standards (eg, 62304), EU Medical Device Regulations and MDSAP + Experience… more
- Abbott (St. Paul, MN)
- …II, Electrical** you will be responsible for designing electromechanical medical devices in Abbott's Electrophysiology medical device division. In this ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Globus Medical, Inc. (Audubon, PA)
- …+ Minimum five years of mechanical design engineering experience, preferably in the medical device field + Bachelor's degree in Mechanical Engineering or similar ... At Globus Medical , we move with a sense of urgency...full compliance with Globus quality system and other applicable regulatory bodies + Design and develop instruments and implants… more
- Globus Medical, Inc. (Audubon, PA)
- …combined with at least 2-3 years of healthcare compliance experience with a medical device or pharmaceutical company. + Compliance and Ethics Professional ... At Globus Medical , we move with a sense of urgency...with internal stakeholders to obtain HCP spend data for regulatory reporting requirements. + International HCP Travel Requests +… more
- GE HealthCare (Waukesha, WI)
- …clinical research, or business development. + Proven experience with Software as a Medical Device (SaMD) development, including regulatory standards (eg, ... delivery of clinically best-in-class algorithms and AI technologies as medical devices algorithm solutions for GE HealthCare... medical technology development, product development in the medical device industry. + Minimum of 5… more
- BioFire Diagnostics, LLC. (Hazelwood, MO)
- …Engineering team develops new equipment, procedures, and test software for IVD medical device products that deliver rapid, high-impact, actionable results in ... + Device Connectivity: Develop software that interfaces with external devices , ensuring robust communication and data handling. + Software Release & Deployment:… more