仕事概要
職種 | 技術職(販売、設計、開発、生産管理)/生産管理、品質管理、施工管理、EHS、PMS |
---|---|
業種 | 医療/ 医療機器 |
雇用形態 | 未分類 |
ポジションレベル | その他 |
募集人数 | 1名 |
希望入社時期 | - |
必須語学力 |
日本語 (流暢に話せるレベル) 英語 (ビジネスレベル) |
活かせる語学 | - |
勤務時間 | その他 |
福利厚生・休暇 | |
ビザ取得支援 | - |
外国人従業員 | - |
仕事詳細
Company Overview
Medical Devices Company
Job Description
• New drug application for approval
• Gap analyses of dossiers provided by overseas sites in comparison with Japanese regulations
• Communication with HAs (negotiations/consultations/meetings)
• GMP application for approval for new drug application/PCA/periodical GMP compliance application
• New application/Renewal of FMA
• Preparation of QA agreement under GQP ordinance
• Manufacture site audit under GQP ordinance
Requirements
Preferable (not mandatory)
• More than 5 years of experience of CMC/Regulatory CMC and more than 2-3 years of experience of QA for pharmaceuticals
• Experiences with MD submission including STED preparation
• Pharmacist
Organizational Knowledge
• Understand the company systems and processes – QA, QC, Marketing, Sales, Customer service, IT, HR, GA, Finance, Manufacturing, Supply chain, Warehouse, Technical Center
• Understand the global culture and different business manner
面接について
連絡先
CMC RA/QA Manager
RGFタレントソリューションズ株式会社
1000 〜 1200 万円