- Abbott (Alameda, CA)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... Device Master Record (DMR) are in compliance with regulatory standards and quality management policies and procedures. +...5+ experience in Software Quality Assurance. + Knowledge of medical device standards including FDA QSR, ISO… more
- Stryker (Ann Arbor, MI)
- The **Principal Software Test Engineer - Embedded Systems / Medical Devices ** will be responsible for leading the verification and validation (V&V) of embedded ... software in our Class I, II, & III medical devices . This role is critical to...focus on **embedded systems.** + 5+ years in the ** medical device ** industry or similarly regulated environment.… more
- Edwards Lifesciences (Seattle, WA)
- …pathology and physiology or Business Unit area of expertise + Moderate understanding of medical device regulatory requirements and documents, device ... + Knowledge of cardiovascular physiology and structural heart anatomy + Previous medical device Clinical Research experience in cardiology + Clinical research… more
- Abbott (Lake Forest, IL)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... in software development, cybersecurity, validation, and/or quality systems in a medical device regulated environment. + Associate's Degree + Experience… more
- BD (Becton, Dickinson and Company) (Tempe, AZ)
- …Science, Math/Stat) * At least 10 years' experience leading a QA organization in the Medical Device Industry * At least 5 years' experience leading FDA or ... and expenditures. * Work closely with leaders in Operations, Regulatory Affairs, Medical Affairs and others to...business outcomes. * Solid business acumen and knowledge of medical device and/or life sciences market environment.… more
- Cook Medical (West Lafayette, IN)
- …of medical writing tasks). Qualifications MD or DO with medical device experience preferred; however, nurse practitioners and physician assistants ... 9-to-5 Eastern Standard Time schedule (Monday through Friday). Responsibilities Provide medical review of clinical and certain regulatory documents (including… more
- BD (Becton, Dickinson and Company) (Irvine, CA)
- …Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health (TM) is our ... of healthcare AI market drivers including reimbursement, pending legislation, economics, regulatory requirements and competition. Analyze their impact on the overall… more
- Philips (Cambridge, MA)
- …debt and prioritizing customer-centric non-functional requirements. + Ensure software compliance with medical regulatory standards like FDA, MDR, IEC 62304 and ... and over 8 years in architectural leadership within the medical device industry. This includes demonstrated success... industry. This includes demonstrated success in bringing software-intensive medical devices to market and leading teams… more
- Philips (San Diego, CA)
- **Senior/Staff Digital Electrical Engineer** **- FPGA for Medical Devices (San Diego, CA)** As a member of an international cross-functional team, you work ... Biomedical Engineering, or a related field. Experience applying IEC 60601-1 and related medical device electronics standards is desirable. + You must be able… more
- Community Health Systems (Tucson, AZ)
- …knowledge (manufacturers, models, modalities, capital planning, etc ) + Understanding of regulatory requirements of medical devices (CMS, TJC, CLIA, ... diagnostic equipment, and laboratory instruments. + Troubleshoots, diagnoses, and repairs malfunctioning medical devices and systems in a timely manner to… more