Aviation Safety Jobs in Tokyo

The PV Associate Japanese speaker should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.). This is an opportunity for new graduates located in Japan to start and develop More...

The PV Associate Japanese speaker should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.). This is an opportunity for new graduates located in Japan to start and develop More...

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join More...

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join More...

Industry: Major Japanese medical device manufacturer Responsibilities: Design and verification of medical devices Molded product design crepe Mechanism design fiber Creation of design documents Design by 3DCAD(Solidworks) Experiments and report writing Creation of various forms More...

Industry: Japanese Leading company of medical device manufacturer Responsibilities: Design and verification of medical devices Creation of design documents Design by electrical CAD(CR8000) Experiments and report writing Creation of various forms Experience with electrical CA Re More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

As People Relations Manager you have complete responsibility and accountability for the People Relations areas for the countries in scope. E.g. implementation of global deliveries and processes policies and guidelines securing that local laws practices and needs are captured and cater More...

As People Relations Manager you have complete responsibility and accountability for the People Relations areas for the countries in scope. E.g. implementation of global deliveries and processes policies and guidelines securing that local laws practices and needs are captured and cater More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

You will lead regulatory affairs services related to the global clinical trials in Japan. Join our team of regulatory experts and contribute to groundbreaking clinical research.Based in Tokyo. Hybrid The scope of responsibilities will include:Develop submission strategies review More...

On this journey were all collaborating to create the best omni customer offer for our customers and as a Construction Project Manager you will be a key player in making this happen. This role is part of the Construction & Facilities (C&F) department supporting all Brands More...

As a Regulatory Officer 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 regulatoryrelated matters. Join PSI and help drive innovation a More...

The Japan Graduate Development Programme (GDP) is a competency framework which supports development needs highlights experience gaps enhances knowledge and gains firsthand experience for graduates. The GDP will run for approximately 24 months starting in April 2026 Graduate Devel More...

As a Regulatory Officer 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 regulatoryrelated matters. Join PSI and help drive innovation a More...

The Japan Graduate Development Programme (GDP) is a competency framework which supports development needs highlights experience gaps enhances knowledge and gains firsthand experience for graduates. The GDP will run for approximately 24 months starting in April 2026 Graduate Devel More...

As a Regulatory Officer 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 regulatoryrelated matters. Join PSI and help drive innovation a More...

As a Regulatory Officer 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 regulatoryrelated matters. Join PSI and help drive innovation a More...