- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist, Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... from concept through launch and post-market surveillance. Key Responsibilities and Activities: The Associate Principal Scientist, Device System - Device Risk… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** GRA Device Lead ( Associate Director ) - Digital Health **Location:** Cambridge, MA/ Morristown, NJ **About the Job** GRA Device Lead ( ... submissions/ device aspects of medicinal product submissions + Liaises with device , clinical , manufacturing, commercial, and other internal business partners… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Principal Scientist, Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management ... concept through launch and post-market surveillance. **Key Responsibilities and Activities:** The Associate Principal Scientist, Device System - Device Risk… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …individual to join the **Patient Safety Strategic Operations** team as an ** Associate Director , Patient Safety Medical Device Safety** responsible ... strategies and ensure operational excellence through successful business partner collaboration. The Associate Director , PS Medical Device Safety will be… more
- Abbott (Princeton, NJ)
- …Abbott is seeking a passionate and driven professional to join our team as ** Associate Director , Market Access and Payer Relations** , supporting the East Coast ... working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more effective, and… more
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . **Position Summary** Reporting to the Director , Inspection Readiness, the Associate Director will ... and collaborate extensively with teams and leaders across the BMS network. The Associate Director will support BMS' GMP/GDP Inspection Readiness strategy by… more
- GRAIL (Trenton, NJ)
- …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... position supports the US Regulatory team in preparing Investigational Device Exemptions (IDEs), IDE supplements, pre-submissions, Premarket Approvals (PMAs), annual… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... + Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial, and public domain information resources to identify relevant… more
- Bristol Myers Squibb (Princeton, NJ)
- …+ Experience working directly with or for pharmaceutical, biotech, or medical device companies. + Prior consulting or architecture leadership experience in Life ... unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency,… more
- Fujifilm (Trenton, NJ)
- **Position Overview** The Associate Clinical Specialist independently provides customer support of Fujifilm's ES equipment in the Endoscopy department and/or ... catalog for assigned customers. It serves as the primary clinical resource for the Company and its sales team...required. This position reports directly to the Zone Sales Director or Regional Manager. **Company Overview** At FUJIFILM Healthcare… more
