Head of Regulatory Affairs

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Published:   2020/05/18


Full time


Medical Device


¥ 17,500,000 negotiable


Head of Regulatory Affairs

  • This position will manage all regulatory activities, including new (first to market in Japan) product submissions and reimbursement activities. You will be responsible for regulatory strategy and delivering on global projects.
  • Tasked with delivering speedy PMDA approvals for good pipeline of aesthetic and ophthalmology products
  • Leads 2 teams - PMDA approvals / QMS (2-3 people and 80% of time) and imported product QA inspections (2 people and 20% of time)\
  • Report to Global RA Head overseas
  • Replacement position with a quick review process.
  • Global market leaders
  • Japan HQ Located in Shinagawa area of Tokyo

Please contact us, we would like to speak with you further about this position, the technology, and see your interest.