The R&D Regulatory Affairs has responsibility for managing products under development and/or marketed products with new indications. · • Develop regulatory strategy for new drug developments, · • Prepare Japanese Common Technical Documents (J-CTD) for the regulatory submission an ...

The R&D Regulatory Affairs has responsibility for managing products under development and/or marketed products with new indications. · At least 2 years for R&D or Regulatory field in a pharmaceutical company or equivalent. · ...

Regulatory project role with regulatory affairs responsibilities in a pharmaceutical company. Develop regulatory strategy for new drug developments and provide regulatory expertise within project/product teams. · Develop regulatory strategy for new drug developments, · Health Aut ...

The R&D Regulatory Affairs has responsibility for managing products under development and/or marketed products with new indications. · ...

This role involves coordinating CMC regulatory strategy activities for assigned projects in Japan. It requires managing relationships with Global CMC to ensure alignment between Japan-Global CMC strategy. · Lead the development of CMC regulatory strategy for assigned projects ens ...

To provide specialist regulatory knowledge and support for chemicals to ensure the regulatory compliance of these materials for both internal and external customers. Learning the requirement of and supporting the CSCL regulatory business. · Generation and submission of regulatory ...

The Company is seeking a Regulatory Affairs Manager to join its team on a full-time basis. The position is responsible for setting & executing the Japan regulatory strategy, managing product registration and maintenance, local regulatory support for the new product launch and loc ...

The Regulatory Affairs Manager is responsible for overseeing the preparation of regulatory submissions required to market new or modified devices in both domestic and international markets including all relevant maintenance activities. · This position will also oversee the prepar ...

The Regulatory Affairs Manager is responsible for overseeing the preparation of regulatory submissions required to market new or modified devices in both domestic and international markets including all relevant maintenance activities.This position will also oversee the preparati ...

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. · ...

The Operations Regulatory Reporting team is responsible for ensuring Société Générale meets its regulatory obligation for key non-financial regulatory reports. · Post Trade Transaction and Position report production and submission. · Monitoring of Report submission schedule and s ...

Are you a seasoned legal professional passionate about energy transition and infrastructure projects? · Our client is a premier developer and operator of energy storage systems, backed by top-tier global investors and driving Japan's decarbonization efforts. · ...

We're looking for the next wave of passionate and ambitious people ready to make a direct impact as a Associate Director Regulatory Affairs CMC. As a member of our team you will be responsible for preparing and/or overseeing the preparation of technically complex regulatory submi ...

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the glob ...

+ Develops innovative Japan regulatory CMC strategies and risk assessments for development projects. · + Assures that positive and collaborative relationships are developed with CMC teams to achieve the implementation of appropriate regulatory strategies. · Key ResponsibilitiesDe ...

The Director of Global Regulatory Chemistry, · Clinical and Controls (GRA-CMC) will be responsible for developing · a global CMC regulatory strategy leading to successful registration · and life-cycle management of unique and technologically complex products. · . · , · ...

Head of Japan Regulatory Strategy for Oncology and Rare Disease. · ...

As a Regulatory Officer, you will work closely with our global team of experts to prepare clinical trial dossiers for regulatory and authorities, deliver regulatory training to project teams, and communicate with stakeholders on regulatory-related matters. · Prepare clinical tria ...

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. · In an industry where cost-cutting and layoffs are common, PSI ...

This role involves working as a specialist in regulatory affairs. · ...

We're totally transforming our business and building our future on smoke-free products with the power to improve the lives of a billion smokers worldwide. · ...