- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and or post go-live support cases in compliance with the company's quality procedures. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a… more
- Sanofi Group (Cambridge, MA)
- …or PhD in LifeScience; Law or Computer Sciences + **Pharmaceutical, biotech, medical device industry experience required** + Demonstrated experience in working ... to generate deeper insights to our Research, Marketing, commercial and medical activities. + Actively monitor North American privacy regulations/enforcements, and… more
- ConvaTec (Lexington, MA)
- …management work this team are subject matter experts in studying how ConvaTec's medical devices interact with the body. Excellent mentoring skille, team work ... technical presentations & reports. + Collaborate with project management, regulatory , clinical, etc. teams to stay aligned on key...where the PhD research topic focused on biomaterials as medical devices . **Team:** No direct reports, but… more
- IQVIA (Boston, MA)
- …for clinical development plans in compliance with applicable regulatory , medical , and ethics guidelines. + Ensure high- quality , data-driven deliverables that ... leaders, and identifying new business opportunities. + Provide due diligence scientific, medical , regulatory , and drug development expertise and activities for… more
- Medtronic (Boston, MA)
- …technical information to both technical and non-technical audience. * Experience in medical device or regulated industry software development is preferred. * ... * Collaborating effectively with cross-functional teams, including hardware, systems, quality , regulatory , and other product development teams; Communicating… more
- Tufts Medicine (Boston, MA)
- …selected institutional guidelines, protocols and policies. + Ensuring compliance with quality and regulatory standards. + Participating in weekly Heart ... focus of providing comprehensive pharmacy services to patients admitted to Tufts Medical Center with Advanced Heart Failure, including patients before, during, and… more
- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more
- Medtronic (Newton, MA)
- …+ Background in electrophysiology, cardiac ablation, or adjacent fields within the medical device industry. + Demonstrated experience leading highly technical ... assurance of software systems, applications, and tools, ensuring compliance with regulatory and quality standards. + Drive continuous improvement in technical… more
- Baystate Health (Springfield, MA)
- …system. **9** ) Assures ongoing compliance with JC, MQSA and ACR regulatory and DPH/CMS requirements. Participates in departmental quality assurance activities. ... exams (as required). Responds to emergency situations (contrast reactions and medical emergencies) according to departmental, clinic and hospital policy. Makes sound… more
- J&J Family of Companies (Woburn, MA)
- …**Qualifications/Requirements:** + 8 + years of related Semiconductor, MEMs manufacturing experience; Medical device experience preferred. + 5 + years of ... management in related technology + Experience managing compliance associated with quality , regulatory , and safety policies + Experience transitioning product… more