We're hiring for Seed Regulatory Specialist - Japan. Obtain the import approval of genetically modified crops through risk assessment required by Japanese government. · Lead preparation and submission of registration dossiers and obtain regulatory approval for the import of genet ...

Regulatory strategy specialist/manager to lead Japanese regulatory strategy and target labeling in J-CDT, share information with Global Regulatory Team (GRT), and prepare CTD for Japan. · ...

Supports the continuity and growth of the business in Asia Pacific by ensuring compliance with regional regulations and advising on regulatory strategy. · Execute transactional processes to ensure day-to-day regulatory compliance. · Provide Product Stewardship & Regulatory (PS&R) ...

The Sr. Business Analyst is an intermediate level position responsible for the overall administrative activities of a business. · Directly supports business managers and generally supports an entire department for the purpose of smooth administrative operation as well as regulato ...

We are developing world-changing technologies that create a more inclusive, trustworthy and sustainable digital society. By designing, engineering and building the world's most complete portfolio of smart devices and infrastructure, we are also leading an Intelligent Transformati ...

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, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in ...

Kenvue is currently recruiting for a Global Regulatory Compliance Auditor. The role involves executing the corporate's Regulatory Compliance audit program, managing audit planning, and identifying potential compliance risks. · ...

Lead Local Trial Manager is a senior trial management role with at least 4 years of clinical trial management experience or more than 6 years of clinical monitoring experience. This role is responsible for local management of a clinical trial (or Medical Affairs data generation a ...

To conduct change control of approved products appropriately as CMC-regulatory affairs (CMC-RA). · ...

To conduct change control of approved products appropriately as CMC-regulatory affairs (CMC-RA). Prepare application dossiers for CMC part and to communicate with HA appropriately to contribute in obtaining regulatory approval. · ...

We are seeking a highly experienced Cluster Lead to oversee functional testing and validation across Legal, Compliance, Client Onboarding, and Treasury Operations domains. · Lead end-to-end functional testing & validation across Legal, Compliance, Client Onboarding, and Treasury ...

Join our dynamic team as a CMC Expert, where you will play a pivotal role in shaping regulatory strategies and ensuring high-quality submissions to authorities like PMDA/MHLW. Leverage your expertise to collaborate with global teams, sharing valuable insights from drug developmen ...

The Associate Director of the Regulatory Affairs (RA) is responsible for the overall management of regulatory affairs activities including pharmacovigilance work at RA department at PDRA division Animal Health in Japan. · Ensure that the RA team develops and successfully executes ...

Embark on a rewarding journey as a Statistical Programmer at Novo Nordisk, where your expertise will drive the success of our clinical trials and ensure compliance with PMDA requirements. · Handle assigned tasks in clinical trial and cross-trial activities, ensuring programming a ...

The Project Lead is a strategic professional who stays abreast of developments within own field and contributes to directional strategy by considering their application in own job and the business. Recognized technical authority for an area within the business. Requires basic com ...

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, where treatments are smarter and less invasive, and solutions are personal. · 担当製品の薬事戦略立案から、薬事申請(承認申 ...

The Functional SME – Front Office provides domain expertise across trade capture, execution, risk monitoring, P&L, position management, and trade validation. The role acts as a bridge between Trading Desks, Risk, Back Office, and IT teams for system implementations, process redes ...

We seek an experienced securities processing Product Owner to work within an Agile framework for this modern real-time event driven securities back-office platform. · Executes product vision as defined by the Securities Processing Group & Product Management team · Work closely wi ...

Johnson & Johnson is recruiting for a Medical Director, Clinical Science Oncology position in Tokyo, Japan. The role involves overseeing clinical studies in Japan and contributing to the global clinical development strategy. The ideal candidate will have a strong background in on ...

The Securities & Derivative Analyst 1 is an entry level position responsible for processing orders and transactions originating from trading desks and branch offices in coordination with the Operations - Transaction Services team. · Perform trade verifications to ensure accuracy ...

The Senior Vice President, Head of Equity Middle Office for Japan, is a senior leadership position responsible for strategically managing and overseeing all aspects of the Equity Middle Office functions within Citi's Japan operations. · Lead and manage a team of Equity Middle Off ...