- Fujifilm (Boston, MA)
- …or processes. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... must have expert level knowledge in all areas of medical informatics, IT infrastructure design and deployment, medical...with MI Project Management (PM) team to deliver high quality Synapse product solutions. + Act as primary technical… more
- Fujifilm (Boston, MA)
- …as assigned. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more
- ConvaTec (Lexington, MA)
- …experience in research and development + Experience developing medical devices under quality systems compliant with ISO 13485 and FDA requirements + Strong ... a research emphasis on biointerfaces and regenerative engineering + Experience in medical device developing and testing **Travel Requirements** Position requires… more
- Fujifilm (Boston, MA)
- …and procedures. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... Knowledge Base articles. + Maintains an expert working knowledge of current medical imaging products and related technologies. + Engineers must have the ability… more
- Tufts Medicine (Boston, MA)
- **Tufts Medical Center** is looking for an **Academic Neonatologist** to join its team at an Assistant or Associate Professor rank. We are seeking an enthusiastic ... Neonatal Network, including the Level IIIb NICU at Tufts Medical Center and five affiliated Level 2 Special Care...nationally recognized with major awards funded by NIH and FDA for genome sequencing, real world data, and novel… more
- Takeda Pharmaceuticals (Boston, MA)
- …knowledge of FDA and ICH regulations and industry standards and quality control principles. + Extensive experience in acquisition, integration, and management of ... + The Director, Third Party Data Acquisition is responsible for timely and high- quality delivery of systems and documentation for non-EDC data in support of Clinical… more
- Actalent (Marlborough, MA)
- …with ASTM/ISTA package testing requirements. + Knowledge of the medical device industry, FDA regulations, quality systems, and sterilization. + ... Skills + Experience working in a technical laboratory or quality role. + Two-year technical degree preferred (AA, AS,...for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and… more
- Capgemini (Waltham, MA)
- …environment, we'd love to hear from you. **Your role** + Design and develop standalone medical device applications using modern C (C 17 or newer) on Linux OS ... Join Capgemini as an Algorithm Software Engineer and help shape the future of medical innovation. In this onsite role based in Boston, MA, you'll contribute to the… more
- Sanofi Group (Cambridge, MA)
- …**About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record of **relevant ... and company activities. + Assists in ensuring product support relationships with FDA are established and maintained. + Provides input into the global organization… more
- Grifols Shared Services North America, Inc (Worcester, MA)
- …submissions. + May supervise staff + May have responsibility for maintaining a compliant medical device quality system for R&D and informing project teams ... strategies for projects and issues affecting development of new products or medical devices or new indications for existing products + Provides regulatory expertise… more