Jim Murray, M.S.c., Consultant

jmurray@gardner.law
‭+1 (612) 810-9032 mobile

Jim has extensive experience in planning and managing projects large and small from product concept through commercialization. He assists companies with manufacturing operations, supply chain management, product development projects, and quality management systems. Jim has held  Operational leadership roles at Mardil Medical Inc., Peytant Systems Inc., Cardiovascular Systems Inc., St. Jude Medical, superDimension (Covidien) and several other medtech startups. Jim is MDR Auditor Training Certified.

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MEDICAL TECHNOLOGIES

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SUPER-G RACE FINISHES

We focus on practical solutions to your project management, operations, and quality systems needs, so you can focus on meeting your business goals.
– Jim Murray, M.Sc.
Practice areas:
  • Operations strategy and operations management
  • Supply chain planning and management
  • New product development program management
  • Quality Management System (QMS) design and implementation
  • QMS assessments
  • QMS software package selection and implementation
  • ERP system implementation
  • Investor Due Diligence

Jim has held Operational leadership roles at Mardil Medical Inc., Peytant Systems Inc., Cardiovascular Systems Inc.,  St. Jude Medical, superDimension (Covidien) and several other medtech startups.

  • Instructor of Design and Manufacturing of Medical Devices as a faculty member for the University of St. Thomas Graduate School
  • Certified Level 3 NICA Mountain Bike Coach and coach for the Roseville Area High School Mountain Bike Race Team
  • Experienced instructor for the Brainerd International Raceway Performance Driving School
  • Associate of Science, Electronic Technology, St. Paul College (St. Paul, Minnesota)
  • Bachelor of Science, Mechanical Engineering, University of Minnesota, Institute of Technology (Minneapolis, Minnesota)
  • Master of Science, Management of Technology, University of Minnesota, Technology Leadership Institute (Minneapolis, Minnesota)
  • EU MDR Auditor Training (Europe’s Medical Device Regulation 2017/745)

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