- Amgen (Cambridge, MA)
- …Qualifications:** + 6-8 years of progressive experience as an engineer or scientist in relevant fields ( medical device development, manufacturing, ... various global manufacturing sites. This role requires a deep understanding of medical device design, manufacturing processes, and regulatory requirements. Key… more
- Capgemini (Burlington, MA)
- …verification strategies, manage a team of engineers, and ensure compliance with medical device regulations. **Your Role** . Lead Verification Strategy: Develop ... systems. . Compliance & Standards: Ensure all verification activities align with relevant medical device regulations such as ISO 13485, IEC 62304, and FDA… more