- Abbott (Plymouth, MN)
- …protocols, reports, specifications, and other project related documentation supporting both new product development projects and sustaining activities. + Acts as ... to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
- Celestica (Richardson, TX)
- …manufacturing engineering and project leadership to ensure robust and high quality product development . Enhance designs with feedback from reviews in areas ... C++ programming skills. + In-depth understanding of Linux kernel, device driver, IPC, U-boot. + Familiarity with Linux application...brings global expertise and insight at every stage of product development - from drawing board to… more
- Samsung SDS America (Ridgefield Park, NJ)
- …solution for mobility lifecycle management-through a combination of strategic partner development with cellular carrier reseller partners and direct engagement with ... + Act as a subject matter expert in enterprise mobility, Mobile Device Lifecycle Management (MDLM), Managed Mobility Services (MMS), and IT workflow automation.… more
- Omnicell (Cranberry Township, PA)
- …creation and maintenance of documentation, and ensuring compliance with relevant medical device regulations + Other duties include troubleshooting, mentoring, ... you will be a key contributor to the design, development , and delivery of innovative, safe, and effective products...experience in a leadership role + Strong understanding of medical device design, regulatory processes, system integration,… more
- Medtronic (Indianapolis, IN)
- …Business is one of the most exciting, dynamic and challenging spaces in the medical device industry. More than 463 million patients worldwide suffer from ... to ensure optimal patient experience + Participates in ongoing competency development through an array of medium including in-person and web-based training… more
- Medtronic (Lafayette, CO)
- …consulting, corporate strategy, or a related strategic role. + Prior experience in the medical device industry. + Strong analytical skills with expertise in data ... stakeholders at all organizational levels. + Experience working in a healthcare, medical device , or technology-focused industry (preferred but not required). +… more
- Astrix Technology (Fort Worth, TX)
- …Certificates (MDD /MDR) and associated documentation. **Key Requirements:** + 4+ years in medical device regulatory affairs + Experience with European MDR and ... 70 + Added - 30/05/2025 Apply for Job Exciting development opportunity to work for a global leader dedicated...leader dedicated to helping people see brilliantly. The largest device company in the world - with complementary businesses… more
- Lilly (Concord, NC)
- …who are determined to make life better for people around the world. **Supervisor, Medical Device Assembly and Packaging** At Lilly, we unite caring with ... have responsibility of supporting start-up activities to bring the Device Assembly and Packaging area into service. This will...all employees if there is a perceived unsafe or product impacting situation. + Responsible for maintaining a safe… more
- J&J Family of Companies (Irvine, CA)
- …years, PhD with at least 2 years of relevant experience required. + Previous medical device Clinical Research experience in the area of interventional cardiology ... the clinical study team; + Cooperates with cross-functional teams (Research & Development , Complaint Handling, Quality/Regulatory, Medical Affairs, Medical … more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …Infusion business. **Key Responsibilities:** + Provide technical leadership for multiple complex medical device platforms in the post-market environment + Lead ... of possible BD is one of the largest global medical technology companies in the world. Advancing the world...possible with us. As Sr. Program Manager of Released Product Management, you will manage activities across a complex… more