Scott Doig
Principal Regulatory Strategy Consultant at Namsa
Based in San Francisco, United States
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Seniority
Director
Department
General Business & Management
Location
San Francisco
Industry
Business Consulting and Services
Company size
1.6K
Contact information
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s•••••••@namsa.com
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Background
About Scott Doig
Dual Citizenship: USA & Canada Highly-experienced leader in development and commercialization of complex, implantable medical devices (devices and drug-device combination products). Managed many cross-functional programs that generated several billion dollars worth of revenue at margins > 80% over my 24 year MDT career (delivery systems, aortic stent grafts, peripheral stents, coronary DES, & coronary DCB). Experienced technical, program, and personnel manager specializing in the development of implantable medical devices. Proven track record developing complex products from conceptualization phase through commercialization in multiple markets including Europe, Asia, Canada, USA, & Japan. Twenty-seven years of medical device development experience including 15 years of combination product development ("drug product") and commercialization experience managing cross-functional teams (drug-eluting stents and drug-coated balloons). Proven track record managing and developing technical professionals of all experience levels and from multiple functions. Responsibilities at Medtronic have also included Advanced Manufacturing Engineering (Process Development and Transfer to Manufacturing Site), Packaging Engineering & Labeling Development, Pilot Manufacturing, and Test Lab Management. Specialties Include: Product Development from Phase 0 through Commercialization in Europe, US, & Japan Medical Device Development Combination Products (Device with Local Drug Delivery) Mechanical Engineering Design Program Management Personnel Management Talent Development Stakeholder Management in a Matrixed Organizational Structure Managing Teams through Regulatory Filings Financial Analysis of Product Development Opportunities Design Verification, Design Validation, Process Development, DOE, Statistical Data Analysis IDE, PMA experience including drug-device combination products MBA, MS Engineering, BS Engineering
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