- AbbVie (Irvine, CA)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Senior Manager is responsible for leading the sustainment, improvement, ... role serves as Deputy Person Responsible for Regulatory Compliance for assigned Device Legal Manufacturer under EU MDR 2017/745, providing compliance subject matter… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Role Overview** The Sr . Director, Clinical Development is an experienced clinical trialist who will be responsible ... development of clinical strategies and plans for assigned programs and work with program teams to ensure integration of clinical strategies and plans into program… more
- Medtronic (Boulder, CO)
- …we not only get the opportunity to manage indirect categories for the largest medical device company in the world, but we also get to experience the immense sense of ... proactively tackle challenges, and bring forward meaningful solutions. As the Sr Strategic Sourcing Specialist-MRO & Operations Category Management, you will: +… more
- Duquesne Light Company (Pittsburgh, PA)
- …better collaboration, innovation and outcomes. We want you to join our team! The Sr End User Analyst IV primary responsibility is to provide technical assistance to ... specialist will take part in the company's critical infostructure end user hardware program . The technical specialist will be asked to take the lead on large-scale… more
- Olympus Corporation of the Americas (Westborough, MA)
- …more about Life at Olympus (https://www.olympusamerica.com/careers) . **Job Description** The Sr Principal R&D Engineer is responsible for contributing to the ... long-term impact. He or she must fully understand medical device design control requirements and be able to effectively...coverage effective on start date + 24/7 Employee Assistance Program + Free live and on-demand Wellbeing Programs +… more
- Medtronic (Los Angeles, CA)
- …breaking down barriers to innovation in a more connected, compassionate world. The Senior Regulatory Affairs Specialist role will both lead and support the review of ... and 4+ years of regulatory affairs experience, preferably with medical device submissions, registrations or advertising and promotional review. OR Advanced Degree… more
- Medtronic (Staten Island, NY)
- …online and field-based training + Performs checks/interrogations of all CRM medical device systems post sign-off + Supports implants of all CRM products post ... Lab setting, or sales or service in a cardiac device company -OR- + Associate's Degree PLUS a minimum...with disabilities. This employer participates in the federal E-Verify program to confirm the identity and employment authorization of… more
- Abbott (Temecula, CA)
- …people in more than 160 countries. **About Abbott** For years, Abbott's medical device businesses have offered technologies that are faster, more effective, and less ... products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier.… more
- Olympus Corporation of the Americas (Washington, DC)
- …US healthcare policy landscape, the ability to communicate complex information with senior government stakeholders, and a high degree of innovation and leadership to ... Monitor and analyze proposed legislation and regulation affecting the medical device sector, including product approval, reimbursement, trade, and compliance. +… more
- Medtronic (Poughkeepsie, NY)
- …a career in sales that changes lives. **A Day in the Life** The Senior Robotic Stapling Specialist is a key technical and strategic expert responsible for driving ... opportunities by working closely with robotic surgery teams. **Market Development Program Execution:** + Initiate and execute district-wide programs, including: +… more