Regulatory Jobs in Japan

Job Description業務内容1. グローバル戦略に沿った効率的かつ付加価値の高い新薬等の国内開発薬事戦略の構築2. 規制当局厚生労働省独立行政法人医薬品医療機器 総合機構などとの窓口業務3. 承認申請審査資料機構相談資料照会事項に対する回答等へのレビューアドバイスを通じ当局提出文書の質の向上に資する4. 承認申請審査...

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...

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...

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...

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...

Career CategoryRegulatoryJob DescriptionGroup PurposeTo support the Regulatory Support Excellence function by ensuring high-quality consistent and efficient execution of Japan Regulatory operations enabling reliable delivery across regulatory activities.薬事本部全体の業務実行を支える基盤として品質一...

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...

DescriptionCooperVision Japan (CVJ) is the largest operating business in the APAC region based in Tokyo and is the second largest single country businesses in worldwide. Japan RA Senior Specialist (hereinafter referred as the RA Senior Specialist) shall be responsible for contributing and leading th...

DescriptionCooperVision Japan (CVJ) is the largest operating business in the APAC region based in Tokyo and is the second largest single country businesses in worldwide. Japan RA Senior Specialist (hereinafter referred as the RA Senior Specialist) shall be responsible for contributing and leading th...

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...

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...

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...

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...