- Oracle (Des Moines, IA)
- …Regulation) + ISO 14971 (risk management) + ISO 13485 + IEC 62304 + SaMD ( Software as a Medical Device) documentation + Experience preparing documentation ... artifacts** , including Design History Files (DHF), Technical Files, Software Architecture documentation , Traceability Matrices, and Verification Plans.… more
- Glendive Medical Center (Glendive, MT)
- …and leadership skills. + Strong customer service orientation. + Proficient with electronic medical record documentation or related software . + Must ... in patient care, etc. + Ability to lift 75 pounds at times. Glendive Medical Center (GMC) conforms to all the laws, statutes, and regulations concerning equal… more
- Oracle (Augusta, ME)
- …you will be a key contributor to the development of and governing the software architecture and compliance framework for regulated medical devices. This role ... support the adoption of compliant SDLC processes and tooling. Deep understanding of medical device software regulations and standards along with a proven… more
- Hologic (Newark, DE)
- Senior Software Engineer, Medical Device Newark, DE, United States Located in Newark, DE, **Hologic** 's Innovation Center is continuing to offer job ... complex issues. + Ability to work with & contribute to appropriate technical documentation (ex: software requirement specifications, software design … more
- Abbott (Burlington, MA)
- … product software (Cloud Patient Care Networks, mobile applications and embedded software ), non- medical software , and non-product software + Support ... their lives. We are seeking an experienced Staff Engineer, Software Design Quality to ensure our medical ... software development plans, and other system and software documentation . + Participate in meetings to… more
- Globus Medical, Inc. (Audubon, PA)
- …integration/unit tests and documentation . + Demonstrate a passion for medical devices and product development, software craftsmanship, and test-driven ... At Globus Medical , we move with a sense of urgency...as possible. **Position Summary:** As a Group Manager of Software , you will be responsible for planning, managing and… more
- US Tech Solutions (San Bruno, CA)
- …Quality System Regulations, ISO 13485, and integration of best practices from the medical device industry. ** Documentation and Support:** 1. Support the creation ... frameworks, and support CAPA, complaints, audits, and overall QMS functions. **Experience:** ** Medical Device Software Experience:** 1. Proven experience in … more
- Globus Medical, Inc. (Audubon, PA)
- …strategies, and documentation + Stays current with advancements in medical robotics, software engineering, and regulatory standards through continuous ... or newer) with strong Qt/QML development skills + Experience building reusable software tools, libraries, and components for medical or robotic applications… more
- ICS (Waltham, MA)
- Senior Project Manager - Medical Device Software Waltham, MA Apply Now Senior Project Manager, Medical Device Software Role SummaryWe are seeking a ... seasoned Senior Project Manager with extensive experience in the medical device / regulated software development sector. In this critical role, you will be… more
- Globus Medical, Inc. (Audubon, PA)
- …and systematic product development. **Essential Functions:** + Design, build, and test software for connected medical devices, ensuring adherence to industry ... team of electrical, mechanical, and software engineers to integrate system software into market-ready medical device products + Evaluate real-world system… more