- Philips (New Kensington, PA)
- …changes, and field safety corrections, with a primary focus on Software as a Medical Device (SaMD) for our Sleep & Respiratory Care products in the US, EU, and Rest ... minimum of 7+ years' experience in Regulatory Affairs/Strategy within FDA regulated Medical Device environments. + You have proven expertise in Software as a Medical… more
- Medtronic (Lafayette, CO)
- …Strong understanding of user experience principles, which arecustomerfacing andadditionallymedical device centered. + Experience with design tools like Figma,Miroor ... experience + Understandingof stage gate processes for projects within the medical device project lifecycle + Documenting design as part of a design history… more
- Philips (Plymouth, MN)
- …in ISO 14971, Risk Management for medical devices and IEC 62304 Medical Device Software. + Serving as SME for Software Design Assurance and collaborate with ... years of experience in Software Quality and/or Software Development in medical device industry with hands on experience with SW Design verification and/or… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …a law firm and/or in-house legal department of a pharmaceutical or device company. + Some experience leading teams and developing/implementing budgets preferred. + ... Broad experience advising commercial and medical functions, including marketing, sales , access and medical. Experience with both pharmaceutical and device … more
- Medtronic (Minneapolis, MN)
- …first-hand how fulfilling and impactful it is to work in the medical device industry. With our expanding portfolio of innovative products and services, Medtronic is ... within a small group to complete a challenging, real-world medical device engineering project + Develop your technical skills through engineering talks,trainingand… more
- Medtronic (Los Angeles, CA)
- …transforms lives Ensure complete and accurate maintenance and reporting of Medical Device Reports (MDRs), Adverse Drug Experience (ADE) data or adverse reaction data ... to meet goals and objectives. Understand current and upcoming Medical Device Reporting (MDRs) and EU Vigilance Reporting requirements by regulatory bodies… more
- Medtronic (Boxborough, MA)
- …test results and recommend quality improvements. Responsible for medical device product verification, developing test protocols, planning, and tracking project ... and cataloging of software defects. Navigate the complexities of various medical device regulations and requirements to include FDA 21 CFR Part 11, ISO… more
- Philips (Plymouth, MN)
- …You have a minimum of 10+ years' experience in FDA regulated medical device environments (drug- device combination products preferred), with a focus on Operations ... coaching, training, etc. + You have strong understanding of Medical Device regulations/standards including ISO 13485/14971, 21CFR (803, 806, 820, etc.), MDD/… more
- Stryker (Columbia, TN)
- …Provides clinical surgical support by managing all relevant equipment. . Anticipates related device needs of the OR staff and surgeon during surgical procedures. . ... routing prior to each procedure. . Adjust camera, monitor, and device settings intraoperatively. . Provide immediate troubleshooting of endoscopy and integration… more
- Adecco US, Inc. (Union City, CA)
- …of the complaint. 6. Perform routine testing of medical devices to replicate reported device complaints and assist in determining the root cause. 7. Review device ... call. 12. Follow up with customers, contracted field service, sales , and marketing personnel regarding part orders and technical...6. Inspection and technical repair experience in the **medical device field is highly desired.** 7. Some travel may… more
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