Responsible for Japan Innovation & Science (QA, Technical Regulatory and Product Development) as well as Japan RPI. Primary responsibility for offering wellness solutions with products and health service. · ...

The incumbent regulatory professional is accountable for Japan strategic management of a portfolio of development projects and post-marketed products within Global regulatory CMC & Devices Japan. · ...

Supports identification and collection of competitive technical product information and provides market-specific claims merchandising information demos and practices for current generation benchmark products.

Formulation design for x-linked polymer systems for lithography applications. · ...

Your main responsibilities as a Technical Bid Engineer will be to ensure timely and correct responses to customer enquiries, prepare clarifications and deviations to tenders, and direct technical negotiations together with Sales Manager and customers. · ...

The GCDSE provides clinical and R&D expertise in their region/country. · Accountable for global protocol development · Ensures consistency across trials in terms of site selection approval process · Responsible for country/regional interactions with regulatory authorities · ...

Develop and implement strategic plans to align brand strategy with market execution. · ...

The Local Safety Officer will serve as a clinical and post-marketing medical safety expert in Japan. They will be responsible for all signal management activities in the country and ensure that local product labels and risk management plans are properly aligned with the benefit r ...

The job involves technical leading regulatory compliance management for Beauty products in Japan. The responsibilities include conducting concept/category reviews, label and claims development, international claims support and investigation of products. · ...

The Japan Sr Project Lead serves as the project leader for development pipelines with comprehensive responsibilities including end-to-end development strategy alignment at both local and global levels. · ...

+Clinical Research Specialist · 治験、市販後臨床研究および市販後調査の計画・実施・進捗管理と報告書作成 · ,担当施設における手続き業務、モニタリングならびに監査対応 · ,関連文書の作成および確認 · ,内部・外部関係者との良好な関係構築 · ,, · ...