Regulatory Activities Jobs in Japan

About the Role:Grade Level (for internal use):09The Team: Customer Experience a core capability within Market Intelligence collaborates closely with the Revenue organization to deliver differentiated customer experience. This group supports our sales teams and business units by overseeing customer s...

JOB DESCRIPTION:Position SummaryThe Regulatory Affairs Senior Specialist is responsible for executing and coordinating global regulatory activities for in vitro Diagnostics (IVD) products for which the company serves as the Legal Manufacturer. The role supports product launches market expansion an...

Career CategoryRegulatoryJob DescriptionHOW MIGHT YOU DEFY IMAGINATIONAmgen is a global leader in biotechnology with a history of more than four decades of pioneering breakthroughs. Our commitment to science has led us to discover and develop innovative therapies that significantly improve patients...

Please submit your application as soon as possible as we reserve the right to close this advertisement at any time.Cochlears mission is to help people hear and be heard. As the global leader in implantable hearing solutions Cochlear is dedicated to helping people with moderate to profound hearing lo...

Why Join UsBe a hero for our rare disease patientsAt Ultragenyx we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to achieve this goal our vision is to lead the future of rare disease medicine. For us this means goi...

ジェンマブは革新的な抗体医薬の開発に注力し患者さんの生活を改善することに力を尽くしています私たちはextranotordinary な未来を共に築くことを使命とし革新的な抗体製品の開発や人々を感動させる抗体医薬品でがんやその他の深刻な病に苦しむ患者さんの生活を根本的に変え治療の未来を切り拓いていますジェンマブは思い...

Career CategoryRegulatoryJob DescriptionGroup PurposeTo prepare scientific and regulatory submission documents that comply with global and local regulatory standardsJob SummaryTo author and gain approval of scientific and regulatory submission documents that comply with global and local regulatory s...

1. Job Objective:Responsible for regulatory activities related to postapproval CMC (Chemistry Manufacturing and Controls) change management for pharmaceutical products contributing to the maintenance of a stable and continuous product supply. 2. Job Roles and Responsibilities:Post approval CMC chang...

Expert Consultant ToxicologyLabcorp is seeking an Expert Consultant Toxicology to join our team in Tokyo or Remote within Japan.Job Responsibilities: Act in Toxicology Expert Consultant Role train mentor and advise junior staff in area of expertise and/or regulatory matters.Provide customer advice...

Job OverviewThis leadership role Director Regulatory Affairs Japan will be a key member of the Japan R&D Development team; Implementation and maintenance of Japan regulatory processes systems and operations in Japan; This role will be responsible for Japan Regulatory strategy for all products. Respo...

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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...

ジェンマブは革新的な抗体医薬の開発に注力し患者さんの生活を改善することに力を尽くしています私たちはextranotordinary な未来を共に築くことを使命とし革新的な抗体製品の開発や人々を感動させる抗体医薬品でがんやその他の深刻な病に苦しむ患者さんの生活を根本的に変え治療の未来を切り拓いていますジェンマブは思い...