- Stryker (Philadelphia, PA)
- …principles that form the ethos of Inari Medical. The Field Clinical Specialist works using independent judgement, partners with local Account Managers to increase ... in increased clinical acumen. **Responsibilities:** + Educate physicians on device handling, implantation and troubleshooting techniques related to Inari products.… more
- Zimmer Biomet (Englewood, CO)
- …strong sense of belonging. **What You Can Expect** The Sr. Regulatory Affairs Specialist serves as the lead regulatory representative on Paragon 28 product and ... practices, and guidelines related to Artificial Intelligence, Software as a Medical Device and Machine Learning (SaMD/ML) + Provide regulatory guidance to product… more
- Robert Half Technology (Portage, MI)
- Description We are looking for a dedicated Staff Specialist in Quality Management Systems to join our team in Portage, Michigan. This long-term contract position ... for healthcare professionals worldwide. Responsibilities: * Create and maintain medical device labeling content that adheres to regulatory and business requirements.… more
- AbbVie (North Chicago, IL)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Specialist Quality Systems is responsible for providing quality assurance support ... products and biologics. Specific areas of support may include the Document Center, Device QA, Labeling, Validation, Training and CAPA. This position will ensure that… more
- Robert Half Technology (Oakland, CA)
- Description About the Role: We are seeking a skilled Endpoint Management Specialist for a one-year temporary assignment to support and evolve our endpoint management ... strategy. This role will be integral in administering mobile device management platforms and ensuring secure, efficient, and user-friendly device configurations… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- **Job Description Summary** As Staff Specialist Regulatory Affairs, you will have a deep understanding of Risk Based frameworks, Agile SDLC, experience with cross ... based multifunction SaMD products to determine compliance with FDA's guidance on device versus non- device functionality. + Prepare, submit, and manage regulatory… more
- Stryker (District Of Columbia, DC)
- The Field Clinical Specialist works using independent judgement, partners with local Account Managers to increase clinical support, education resulting in increased ... clinical acumen.ResponsibilitiesEducate physicians on device handling, implantation and troubleshooting techniques related to Inari products.Develop, lead and/or… more
- Medtronic (MN)
- …of a dynamic team responsible for training and educating our sales and clinical specialist teams in the field of cardiac ablation to treat arrhythmias, one of the ... in a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience -OR- + Associate's Degree PLUS a… more
- Abbott (St. Paul, MN)
- …health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease. The Opportunity ... - We are seeking a Regulatory Operations Specialist I for our St. Paul, MN Structural Heart team to perform specialized level work assignments and/or analyses,… more
- DEKA Research & Development (Manchester, NH)
- …part of creating innovative medical solutions! As our Quality Documentation Control Specialist , you'll play a vital role in maintaining regulatory compliance through ... meticulous document control processes in our medical device R&D environment. You'll work collaboratively with cross-functional teams to ensure documentation accuracy… more