Sr Regulatory Affairs Specialist - Cardiac Diagnostics Cdx jobs at Boston Scientific in United States, Arden Hills
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United States
State
Arden Hills
72 jobs found
26.06.2024
BS
Boston Scientific Sr Regulatory Affairs Specialist - Cardiac Diagnostics CDx United States, Minnesota, Arden Hills
Supports the development of domestic and international strategies for regulatory approval of Class I, II and III medical devices. Coordinates, compiles, and submits U.S. and EU regulatory filings for new...
Demonstrating analytical expertise by utilizing large datasets to draw conclusions about product-related assessments, with a focus on meticulous collection, organization, and analysis of substantial information, ensuring detail and accuracy. Analyzing...
Manages the full project lifecycle, including initiating, planning, executing, controlling, and closing processes, while building team ownership and commitment. Estimates project effort and resources using standard estimating techniques and collaborates...
Manages the full project lifecycle, including initiating, planning, executing, controlling, and closing processes, while building team ownership and commitment. Estimates project effort and resources using standard estimating techniques and collaborates...
Leadership – Develop and execute strategies to create high-performing functional teams. Establish team goals to support overall business objectives. Lead functional managers through mentoring, talent development/retention, and performance management. Product...
Identify and proactively propose strategic approaches to key business challenges and opportunities. Lead cross-functional teams to launch product enhancements and other key marketing initiatives; clearly scope strategies and implementation plans,...
Perform as the Regulatory Affairs Lead team member on initiatives to transform how we address the unique needs of capital equipment life cycle within the quality system (from part creation,...
Supports the development of domestic and international strategies for regulatory approval of Class I, II and III medical devices. Coordinates, compiles, and submits U.S. and EU regulatory filings for new...
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