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CMC/QC担当者 （バイオ医薬・再生医療）
| Hiring Company | 非公開 |
| Location | Tokyo - 23 Wards |
| Job Type | Permanent Full-time |
| Salary | 6 million yen ~ 9 million yen |
Job Description
【求人No NJB2361836】
■仕事内容
タンパク医薬品の上市に向けて細胞株からプロセス開発、及び製造を含めた品質管理
タンパク医薬品を委託先（CDMO）と連携して開発・製造を推進
PMDA 対応：承認・一変申請書の作成、照会対応、品質相談など
General Requirements
| Minimum Experience Level | No experience |
| Career Level | Mid Career |
| Minimum English Level | Business Level |
| Minimum Japanese Level | Native |
| Minimum Education Level | Bachelor's Degree |
| Visa Status | Permission to work in Japan required |
Required Skills
■必要条件
・製薬企業・バイオベンチャー・CDMO にて、GMP 下でのタンパク医薬品の細胞株構築、
・プロセス開発、製造などの品質管理業務にかかる業務経験
・英語でのコミュニケーション、文書作成
■歓迎条件
・分子生物学、タンパク質工学や細胞発現などに関する知識
・バイオ医薬品の開発や製造に係る業務経験
・PMDA 相談（品質）の経験
Job Location
- Tokyo - 23 Wards
Work Conditions
| Job Type | Permanent Full-time |
| Salary | 6 million yen ~ 9 million yen |
| Work Hours | 09:00 ～ 17:30 |
| Holidays | 詳細は求人ご紹介時にご案内いたします。 |
| Industry | Pharmaceutical |
