- Medtronic (Boston, MA)
- …+ Maintain up-to-date knowledge of cybersecurity regulations and standards specific to the medical device industry (FDA, HIPAA, IEC 62443, NIST, NIS 2, etc.). ... GRC (Governance, Risk, & Compliance), or external/internal audit, preferably within the medical device or healthcare industry. + Strong understanding of… more
- Medtronic (Boston, MA)
- …multiple teams to execute concurrent, interdependent projects. + Knowledge of medical device R&D, product development, and clinical/regulatory procedures; ... across each milestone. Join our esteemed team as a Principal Project Manager within the Robotic Surgical Technologies (RST)...as a Subject Matter Expert + Comprehensive knowledge of medical device standards and regulations (eg, IEC… more
- Philips (Cambridge, MA)
- …of 8+ years' Regulatory Affairs experience within FDA regulated Medical Device /HealthTech product environments. Experience with Software as Medical ... critical member of the Philips Ultrasound- Regulatory Affairs Organization, the Principal Regulatory Affairs Specialist will lead and provide regulatory oversight… more
- Medtronic (Boston, MA)
- …management files and applying risk management best practices and principals to medical device development + Demonstrated expertise in new product development ... a lasting impact. Medtronic is looking for a Senior Principal Systems Engineer. This role will collaborate across the...of complex, software controlled electromechanical systems; ideally systems of systems +… more
- J&J Family of Companies (Danvers, MA)
- …a related field. + 10+ years of experience in process validation within the medical device industry, with a focus on electro-mechanical systems. + Demonstrated ... States of America **Job Description:** Johnson & Johnson is currently seeking a Principal Validation Engineer to join our Heart Recovery team located in Danvers, MA.… more
- Cardinal Health (Mansfield, MA)
- …Services Center perform laboratory testing to characterize the chemistries of our medical device products and stability testing for pharmaceutical products of ... protocols utilizing specialized instrumentation and analytical techniques to characterize medical devices, materials, and processing aids for chemical properties of… more
- Fresenius Medical Center (Lawrence, MA)
- …staffing and leading a team of software developers to deliver high quality medical device software . Develop and drive a long-term strategic vision for ... development, verification, and standards necessary to meet global medical device regulatory requirements. + Clear understanding of Software Development and… more
- Fresenius Medical Center (Lawrence, MA)
- …Partner for Software as a Medical Device and Non- medical software device engineering teams to ensure compliant products, engineering teams ... Post Market Surveillance activities are performed, and actions derived ** PRINCIPAL DUTIES AND RESPONSIBILITIES** . Works as part of... DUTIES AND RESPONSIBILITIES** . Works as part of software development team on new product development or on… more