- Fujifilm (Bothell, WA)
- …**Essential Job Functions:** + Apply understanding of the fundamentals of medical device reprocessing to establish cleaning and disinfection procedures ... and processes comply with applicable industry guidance, standards, and regulations on medical device reprocessing. + Provide guidance to design teams when… more
- J&J Family of Companies (Raritan, NJ)
- …Stay updated on industry trends, emerging technologies, and regulatory changes impacting the medical device sector. + Provide strategic updates and insights to ... + A minimum of 8 years of experience in a regulated industry ( medical device , biopharmaceutical, or pharmaceutical), with experience in a technical leadership… more
- Teleflex (Coventry, CT)
- …is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades ... is preferred or 3+ years of Quality Assurance experience working in the medical device manufacturing environment (a combination of education and experience will… more
- Cognizant (Melbourne, FL)
- …gather, analyze, and document requirements for software development in a regulated medical device environment. This role demands quick learning, strong ... user stories to ensure clarity and alignment across teams. . Ensure compliance with medical device software regulations (21 CFR Part 820, ISO 13485). . Act as a… more
- Medtronic (Indianapolis, IN)
- …**Nice to Have (Preferred Qualifications):** + Experience at Medtronic or within the medical device industry + Experience in the management of clinical devices. ... drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion...for all ablation procedures at study sites for investigational device studies to guide the physician on the requirements… more
- BD (Becton, Dickinson and Company) (Durham, NC)
- …a positive and professional demeanor, and is willing to learn about BD medical device instrumentation and applications. A successful candidate will work under ... technology and devices. They work to design, develop, and test medical devices while following medical device regulations and quality processes. An EDP will… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …Technical Files, etc.) + Develop and implement global regulatory strategy for MMS Dispensing Medical Device and non- Medical device products and software ... effort to comply with new and existing regulations (eg, FDA Medical Device Regulations, EU-MDR) + Support the monitoring, interpreting, and implementing of… more
- AbbVie (Florham Park, NJ)
- …position is responsible for the operations and strategic design of the US Medical Device & Aesthetics businesses global supply planning organization which ... support very significant revenue streams for Medical Device & Aesthetics businesses. Achieving the revenue goals are critical to AbbVie's top line revenue goals… more
- Oura (San Francisco, CA)
- …digital health products, including wearable devices and related software, including Software as a Medical Device (SaMD), Software in a Medical Device ... and Good Manufacturing Practices (GMPs), as well as post-market compliance, including Medical Device Reporting (MDR), product recalls, corrective actions, and… more
- Oura (New York, NY)
- …are compliant with the applicable standards and regulations governing the development of medical device software at Oura. This role will demand close ... have: + 5+ years of experience working in a regulated environment under a medical device Quality Management System (21 CFR 820 or ISO 13485:2016) as a project… more