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Kaoru Horiba profile image

Kaoru Horiba

Director of Reguratory Affais, Quality Assurance, Clinical Affairs and Technical support at MicroPort
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Location
Yokohama, Kanagawa, Japan, JP
Skills
  • Clinical Trials
  • Medical Compliance
  • Regulatory Affairs
  • Reimbursement Of Medical Device
  • Cross Functional Team Leadership
  • Show all
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Bio

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Experience

  • MicroPort
    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • Director of Reguratory Affais, Quality Assurance, Clinical Affairs and Technical support
      • Sep 2020 - Present

    • Director of Regulatory Affairs, Quality Management and Technical Support
      • Mar 2019 - Present

  • Cochlear
    • Director RA, QA and reimbursement
      • Feb 2016 - Feb 2019

  • Hollister Incorporated
    • Livetyville and Tokyo
    • Director Regulatory Affairs and Legal/Compliance
      • Jun 2013 - Jan 2016
      • Livetyville and Tokyo

  • Zimmer Biomet
    • Tokyo
    • Associate Director Regulatory Affairs
      • Apr 2012 - Jun 2013
      • Tokyo

  • Johnson & Johnson OCD
    • Tokyo
    • Senior Manager Regulatory Affairs
      • Sep 2007 - Apr 2012
      • Tokyo

  • Brainlab
    • Tokyo
    • Manager QM and RA
      • Sep 2004 - Sep 2007
      • Tokyo

  • Medtronic
    • Kawasaki
    • Supervisor Clinical Affairs and RA functional support
      • Apr 2002 - Jun 2004
      • Kawasaki

  • Covidien (Medtronic Minimally Invasive Therapies Group)
    • Tokyo
    • Associate Manager RA, QA and Pre-clinical development
      • Jan 2000 - Apr 2002
      • Tokyo

  • OTSUKA PHARMACEUTICAL COMPANY LIMITED
    • Nagoya and Takasaki
    • Specialist Clinical Affairs
      • Jun 1988 - Mar 1991
      • Nagoya and Takasaki

Education

  • Bond University
    Master of Business Administration - MBA, Business Administration and Management, General
  • Meijo University
    Bachelor of Pharmacy - BPharm, Pharmacy

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Industry Focus. “Medical Equipment Manufacturing”

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