Principal Regulatory Affairs Specialist - Endoscopy jobs at Boston Scientific in United States, Marlborough
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Company (1)
Job type
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Job title (1)
United States
State
Marlborough
43 jobs found
28.08.2024
BS
Boston Scientific Principal Regulatory Affairs Specialist - Endoscopy United States, Massachusetts, Marlborough
Under minimal supervision, acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, clarification and follow...
Collect customer and cross functional insights as relevant, including customer insights (VOC/MR), Competitive landscape, Reimbursement landscape, Commercial/franchise objectives. Partner with internal teams to develop VAT insights via the Value Analysis...
Encompasses Virtual Reality platforms & customized content development, as well as other Experiential Tech & Programs that empower BSC to deploy Mixed Reality (MR) and VR hardware, along with immersive...
Leading and managing a functional interaction and engagement with the Magellan Project, typically collaborating with team leads / product owners. Aligning on requirements and influencing the Magellan Development Teams to...
Publish & manage content (videos, PDFs, SCORM) on EDUCARE platform; assign eLearning curriculums and manage inquiries from the field and HCP customers. Evaluate curricula for appropriate assignment and timing; monitor...
Rising Senior students currently enrolled in an undergraduate degree program in Business / Sales. Ability to work in the US permanently without any restrictions. Manage a project in our Sales...
Rising seniors working towards a Bachelor’s degree with an Engineering focus. Ability to work in the US permanently without any restrictions. Corporate housing & relocation assistance or a living stipend...
Under minimal supervision, acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, clarification and follow...
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