About this role
薬事エキスパート at Medline. Location: Tokyo, Tokyo, Japan. Role: Prepare submissions, Coordinate with authorities, Support QMS conformity Requirements: Experience in regulatory submissions for medical devices, handling end-to-end filings, and English communication with overseas manufacturers. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Word, Excel, PowerPoint, Outlook Commitment: Full Time Workplace: Hybrid Languages: English, Japanese