[Japan] 文書管理担当者(QMS・GLP・信頼性基準関連資料)

Manage QMS and GLP document processes, including ISO survey coordination, regulatory document storage, and response to regulatory authority inquiries. Oversee the Nara R&D Center archive room for GMP, reliability standards, and Non-GxP documents. Administer the VQD (Vault QualityDocs) system for operational maintenance, CSV activities, and training. Maintain relevant SOPs and lead business improvement initiatives to enhance quality and productivity in assigned tasks. Requires weekly in-office attendance three times or more, with remote work available otherwise. Candidates must possess experience in document management procedures and proficiency in Microsoft Office for structured document creation, data analysis, and presentation design.