Animal Health, Regulatory Affairs - Chiyoda
16時間前

Job summary
The Associate Director of Regulatory Affairs is responsible for managing regulatory affairs activities including pharmacovigilance work at Animal Health in Japan.
- Motivate and encourage RA Team performance.
- Develop project plans for timely product registrations
求人説明
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
すべての上級職にアクセスして、理想の仕事を手に入れましょう。
似たような仕事
当社は革新的な医療技術を通じて医療現場の課題解決に貢献するグローバルメドテック企業です。 · 本ポジションでは医療機器のISO13485に基づく品質マネジメントシステム(QMS)の運用および改善を担当いただきます。QMS文書を作成・改訂し続続的なプロセス改善を行うことができます。また手順書を作り規制対応を行い、および輸送管理安全管理(Vigilance)まで幅広い領域で仕事をすることができます。 · ...
+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. · +Support PDRA director to optimize/maximize PDRA's activities ...
Ethicon Wound Closure & Healing and Biosurgery is seeking a dynamic and experienced Senior Manager or Associate Director to join our Regulatory Affairs team in Japan. · ...
The Associate Director, Regulatory Affairs CMC will primarily be responsible for managing regulatory CMC submissions and strategy for Incyte development and marketed products.Ensures compliance to global regulatory guidance documents, regulations and laws as well as internal poli ...
· 商用運航開始(EIS)に向けた事業基盤構築、運航関連法規の適合性確保、およびカスタマーサポート体制の確立を統括する。 · ...
We are seeking a Director of Immunology Medical Affairs to lead our medical affairs strategy for immunology therapeutic areas. This role will involve collaborating with internal and external stakeholders to develop and implement overall medical affairs strategies for product life ...
The Manager/Specialist of Medical Affairs will conduct medical affairs activities for Janssen Hematology brands primarily focused on proper usage and value maximization. · Develop overall strategy for Hematology portfolio to address medical and scientific issues. · Collaborate wi ...
This is an exciting opportunity for an Experienced Labeling Specialist to join our team at Johnson & Johnson. As part of the Regulatory Affairs Group, you will work closely with global teams to develop Japanese package inserts (PI) and collaborate with partners in Japan. · Develo ...
The Manager/Specialist of Medical Affairs, Hematology will be responsible for conducting Medical Affairs (MA) activities for the Janssen Hematology brands primarily focused on proper usage and value maximization. · The Manager/Specialist will be an expert in medical strategy deve ...
The Labeling Specialist will develop Japanese package inserts based on Japanese target labels and run Japan Labeling committee process to develop labeling positions for marketed product issues. · Develop J-PI from Japanese Target Label · Run Japan Labeling committee process to de ...
Kenvue is currently recruiting for a Manager Medical and Safety Sciences. · This role involves leading research projects to ensure compliance with safety standards, · managing laboratory teams to deliver high-quality scientific data, · and driving project timelines. · Maintain an ...
The Associate Director, Capability & Digital Excellence (CDE) leads a specialized team within the Medical Operations Excellence (MOE) department of Medical Affairs (MAF).This role is accountable for two strategic areas—Capability Development and Digital Transformation. · ...
We are in search of our newest team member for the Market Access & External Affairs division to become a part of our Public Affairs, Industry Policy group. In this role, you will collaborate with a wide range of stakeholders across the healthcare industrial sector to help shape a ...
The Associate Director,Capability & Digital Excellence(CDE) leads a specialized team within the Medical Operations Excellence (MOE) department of Medical Affairs (MAF). This role is accountable for two strategic areas—Capability Development and Digital Transformation, · Lead the ...
The Labeling Specialist develops Japanese package inserts based on Japanese target labels and collaborates with Global Labeling for creation/revision of labeling positions. · Under supervision:Develops J-PI based on JTL. · Runs Japan Labeling Committee process. · ...
The IEGP lead serves as a key partner to MAF-TA to support developing cross-functional IEGP and to manage study progress such as study milestones and budgets by ensuring the governance and process. · ...
A Lead Local Trial Manager or Senior Local Trial Manager is responsible for local management of a clinical trial in a country or countries. · ...
The Manager will lead insight analytic function within Medical Affairs (MAF), delivering timely accurate actionable insights inform strategic decision making. · The role responsible designing operationalizing AI-driven solutions/automation produce measurable business outcomes. ...
A Lead Local Trial Manager is considered as a senior trial management role with at least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience. · ...
At Johnson & Johnson we believe health is everything Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented treated and cured Through our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across th ...