Biotechnology Research Jobs in Japan

Job OverviewThis leadership role Director Regulatory Affairs Japan will be a key member of the Japan R&D Development team; Implementation and maintenance of Japan regulatory processes systems and operations in Japan; This role will be responsible for Japan Regulatory strategy for all products. Respo...

職務内容HIV/AIDS領域においてUNAIDS国連エイズ合同計画の目標の日本国内における達成とHIVと共に生きる人々PLHIVのQOL向上に寄与する活動ViiV Portfolio/Pipelineの価値の最大化とヘルスケアエコシステムの構築のためのためのPolicy shapingおよび社外ステークホルダーとのコミュニケーションマネジメント会社のMission/Pu...

Make your mark for patients患者さんのためにあなたの力を発揮してくださいAbout the roleWe are looking for a Head of Regulatory Affairs who is strategic collaborative and peoplefocused to join our Regulatory Affairs team based in our Nishi-Shinjuku office in Tokyo Japan.You will lead the regulatory str...

Work Flexibility: Hybrid or OnsiteThe Jobs MissionUnder minimum supervision by Manager he/she understands the related laws and regulations and efficiently conducts the duties such approval applications notifications and other related tasks.マネジャーの最小の指導の下薬機法全般に精通し豊富な知識と経験...

Job SummaryAre you passionate about advancing health and wellness through innovative bioscience solutionsIFF is a global leader in flavors fragrances food ingredients and health & biosciences. We deliver sustainable innovations that elevate everyday products.Health & Biosciences (H&B) is dedicated t...

Position PurposeThis role drives strategic pricing decisions that accelerate patient access to Pfizers products and safeguard business value while shaping pro-innovation pricing frameworks with the Ministry of Health Labor and Welfare (MHLW) and industry stakeholders.ResponsibilitiesDevelop and exec...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment appl...

By clicking the Apply button I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takedas Privacy Notice and Terms of Use. I further attest that all information I submit in my employment ap...

ABOUT THE ROLE日本におけるホテルポートフォリオの拡大をリードする開発ディレクターを募集しています本ポジションはAccorの全ブランドを対象にさまざまな契約形態運営受託フランチャイズレジデンスやプロジェクトタイプホテルリゾート長期滞在型ブランドレジデンス複合開発に関する開発案件の獲得交渉契約締結までを担う...

Job DescriptionPOSITION OVERVIEW:The Associate Director of the Regulatory Affairs (RA) is responsible for the management of regulatory affairs activities including pharmacovigilance work at RA department at PDRA division of Animal Health in Japan. The position requires a combination of scientific kn...

We are seeking an experienced and detail-oriented Manager Regulatory Submission Project Management (RSPM) to join our dynamic team. This pivotal role offers the opportunity to lead the planning execution and review of regulatory operations activities ensuring the successful submission of regulatory...

As part of our global expansion we are now looking for in-country regulatory professionals to join our growing global regulatory team. This is an exciting opportunity to demonstrate your knowledge in leading regulatory processes for biological products and regenerative medicines in Japan and to buil...

At Google DeepMind we value diversity of experience knowledge backgrounds and perspectives and harness these qualities to create extraordinary impact. We are committed to equal employment opportunities regardless of sex race religion or belief ethnic or national origin disability age citizenship mar...

Job Descriptionジェネラル&スペシャルティメディスン以下GSMは当社の重点分野の1つでありこれまでに多くの革新的な医薬品の発売や適応症および対象疾患の拡大に取り組んできましたこの度はGSM領域を担当いただくMSLメディカルサイエンスリエゾンチームのマネージャーを募集します私たちの仕事は患者さんの生命を脅かす病気...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Position Summary Senior Manager Regulatory Affairs should be responsible for creating Japanese Package Inserts (JPIs; i.e. Japanese Labeling) of new drugs and manage revisions of JPIs of post approval products and review of educational materials ( with the advice of Director or Associate Director as...

会社紹介ビジョン私たちIQVIAはヒューマンデータサイエンスの先駆的な企業として医療ヘルスケアの前進に取り組む皆様をIQVIAならではの革新的なソリューションによってご支援することで誰もがより健康に自分らしく生きられる社会の実現を目指しています世界最大規模を誇る医療ヘルスケア関連データを基盤に人データサイエン...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Position Purpose: The Regulatory CMC Expert evaluates all CMC regulatory aspects related to the assigned products (including both development products and established products) in Japan.The Regulatory CMC Expert develops and executes CMC strategies for development products/life-cycle management of e...