Senior Senior Director Medical Affairs jobs at Boston Scientific in United States, Massachusetts, Marlborough
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Company (1)
Job type (1)
Job categories
Job title (1)
United States
Massachusetts
Marlborough
8 jobs found
16.05.2024
BS
Boston Scientific Sr Regulatory Affairs Specialist - Endoscopy United States, Massachusetts, Marlborough
Act as company representative under minimal supervision, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, and submission review....
Serve as the primary business partner in forecasting, reporting and consulting for Global HR, Legal, and other smaller administrative functions (i.e. Community Engagement, Close the Gap). Perform all aspects of...
Assist with the planning and preparation of periodic SEC reporting documents including Forms 10-Q and 10-K and support the earnings release and proxy process and other ad-hoc filings throughout the...
Strategic Leadership: Develop and execute strategies aimed at the widespread adoption and integration of Generative AI, Intelligent Automation, and Process Optimization principles throughout the organization. Engagement and Education: Lead initiatives...
Leading IT sourcing specialists in category strategy development, strategic sourcing, and major contracts negotiations. Establishing cross-functional sourcing teams to evaluate and onboard suppliers to support project timelines, manage cost and...
Work closely with and observe clinicians and hospital staff in their environment to understand their needs and pain points. Develop user profiles and use flow analysis of clinical staff in...
Acts as a Business Analyst in managing SuccessFactors modules and delivery of HR Technology projects; includes primary ownership of module configuration, system validation, and user acceptance testing (UAT) sign off....
Act as company representative under minimal supervision, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, and submission review....
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