- Amazon (Seattle, WA)
- …in a variety of areas, few examples would be: hardware design and development ; building the systems that validate hardware quality in manufacturing; monitoring and ... smoothly and minimize or eliminate customer impact due to device related issues for a transparent AWS customer experience....a member of the UC organization, you'll support the development and management of Compute, Database, Storage, Internet of… more
- Medtronic (Minneapolis, MN)
- …calculations and applies appropriate accounting principles to outputs. Understand global medical device market drivers related to technology advancements, market ... MN, operates with limited supervision as the primary contact for Corporate Development leading critical aspects of mergers and acquisitions, joint ventures, minority… more
- Nissha Medical Technologies (Colorado Springs, CO)
- …+ Works with engineers to develop assembly and alignment methods for complex medical device assemblies and sub-assemblies. + Contributes technical expertise in ... the development and implementation of new processes. + Organizes, coordinates,...attendance is required. **REQUIREMENTS:** + Prior experience in a medical device manufacturing environment + Experience in… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... required. + Software implementation experience required. + Experience in medical device manufacturing and knowledge of GxP...knowledge of GxP compliance and FDA process validations, including development and execution of protocols is a plus. +… more
- Fresenius Medical Center (Lawrence, MA)
- …remotely. **PURPOSE AND SCOPE** Act as a Quality Business Partner for Software as a Medical Device and Non- medical software device engineering teams to ... DUTIES AND RESPONSIBILITIES** . Works as part of software development team on new product development or on design changes to ensure product quality and… more
- Cook Medical (Bloomington, IN)
- …clinical, and regulatory affairs.- Provide leadership in the understanding of medical device regulations and best practices.- Manage conflict resolution ... Qualifications - Engineer degree and 5-8 years of experience- Demonstrates knowledge of medical device regulation (ISO 13485, 21CFR) and risk management (ISO… more
- Cook Medical (Ellettsville, IN)
- …clinical, and regulatory affairs.* Provide leadership in the understanding of medical device regulations and best practices* Manage conflict resolution ... Qualifications * Bachelors degree in a scientific discipline* Demonstrates knowledge of medical device regulation (ISO 13485, 21CFR) and risk management (ISO… more
- ZOLL Medical Corporation (Deerfield, WI)
- …to understand the appropriate legal and regulatory requirements in the areas of medical device operations and to establish robust processes and controls to ... discipline required + Experience in an FDA regulated Class III electrical medical device manufacturing environment required and + Experienced in process… more
- Cook Medical (West Lafayette, IN)
- …with and apply global emerging PFAS regulations + Involvement with AdvaMed, Medical Device Manufacturers Association, or equivalent advocacy groups or standards ... surfaces for polymer technologies preferred + Previous involvement with AdvaMed, Medical Device Manufacturers Association, or equivalent advocacy groups or… more
- GE HealthCare (Florence, SC)
- …Implement qualification and validation processes achieving compliance with ISO and other medical device standards; Data analysis to identify trends and insights ... in the manufacturing and design of superconducting magnets, cryostat devices, or similar medical devices. Work experience to include: 3D designs in CREO or CAD to… more