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Hiring Company | 外資系大手ライフサイエンス企業 |
Location | Tokyo - 23 Wards |
Job Type | Permanent Full-time |
Salary | 5.5 million yen ~ 8.5 million yen |
【求人No NJB2284784】
・Assisting in maintaining the QMS on site implementing local solutions where required
・Work with Quality Systems such as Document Control
・Work within Global eQMS and eDMS/eTMS systems
・Provide support for internal external (Regulatory/Notified body) and supplier audits
・Provide support for activities such as Supplier Management electronic signature etc.
・Actively participate as a member of the QA team on site in partnership with both the Site Head and Global QA Sr. Director
・Participate in local project implementations and/or be part of larger project teams
・Act as subject matter expert/intermediary in communications between Regulatory/Notified bodies and overseas manufacturing sites
・Work with the Warehouse/3PL team on a daily basis to ensure smooth running of activities (including product release and re labelling)
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 |
■必須要件
・2 years experience in Quality Affairs preferably in a regulated IVD/MD company
・Good spoken and written English ability
・Holder of Pharmaceutical license would be a bonus
■歓迎要件
・Pharmacist license
Job Type | Permanent Full-time |
Salary | 5.5 million yen ~ 8.5 million yen |
Work Hours | 09:00 ~ 17:45 |
Holidays | 【有給休暇】有給休暇は入社後4ヶ月目から付与されます 初年度 10日 4ヶ月目から 【休日】土 日 祝日 夏季休暇 年末年始 … |
Industry | Pharmaceutical |
Company Type | International Company |