CareerCross uses cookies to enhance your experience on our websites. If you continue to view our sites without changing your browser settings, then it is assumed that we have your consent to collect and utilise your cookies. If you do not want to give us your consent, then please change the cookie settings on your browser. Please refer to our privacy policy for more information.
CareerCross uses cookies to enhance your experience on our websites. If you continue to view our sites without changing your browser settings, then it is assumed that we have your consent to collect and utilise your cookies. If you do not want to give us your consent, then please change the cookie settings on your browser. Please refer to our privacy policy for more information.
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】
■バイオシミラー製品の他、再生医療製品等にも携わることができます。
■仕事内容
タンパク医薬品または再生医療等製品の上市に向けた開発、品質管理
タンパク医薬品または再生医療等製品を委託先（CDMO）と開発・製造の推進
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または再生医療等製品のプロセス開発、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
分子生物学に関する知識、タンパク質や細胞を実務経験
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 |
