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事業実施状況の確認をお願いするお仕事です。全国の事業者の確認をおねがいするので、宿泊を伴う出張もあります。平日のみ週5日9:00~17:30(休憩60分)小休憩10分あり(有給)、残業は月15h程度(1分単位で給与計算) · ...

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The CMC RA Manager will lead and manage CMC regulatory activities, develop and implement CMC registration strategies, and support the development of the CMCRA team. The ideal candidate will have +10 years of practical experience with CMC-related roles, experience drafting and com ...

Lead and manage CMC regulatory activities including relevant cross-functional communication, providing guidance across the product lifecycle, and ensuring timely regulatory compliance with official guidelines. Develop and implement CMC registration strategies related to CTNs, NDA ...

The Quality Administrator will be responsible for performing various administrative tasks, including creating and managing files, handling complaints, and conducting investigations. They will also be responsible for creating and distributing daily reports, as well as managing and ...

We are seeking a RegulatoryAffairs Specialist to join our team at JohnsonandJohnson.The successful candidate will be responsible for maintainingand managing regulatory approvals for pharmaceutical products including surgical suturesand adhesives. · ...

+This role involves maintaining regulatory approvals for general surgery products including sutures and tissue adhesives. · +Promptly managing regulatory compliance activities across various regions. · Establishing strong relationships with key stakeholders within local authoriti ...

+ · The company seeks an experienced professional for its regulatory affairs team responsible for maintaining management of Japan general surgery field products including sutures tissue adhesives etc. ...

The HR Generalist will be responsible for maintaining employee data, creating employment contracts, and managing employee benefits. The role will also involve coordinating new hire onboarding, managing employee offboarding, and providing support for business letters and other HR- ...

We are seeking a highly skilled and experienced R&D Oncology Clinical Science Clinical Research Sr. Scientist to join our team. The successful candidate will be responsible for developing and implementing clinical research strategies, collaborating with cross-functional teams, an ...

Contribute to the development of innovative new drugs for cancer treatment through collaboration with various departments. Develop and implement clinical trial plans, and work closely with internal and external stakeholders to achieve project goals. · Develop and implement clinic ...

We are seeking a Financial Controller for our Tokyo office. This role offers the opportunity to lead finance operations in Japan, reporting directly to the Asia Corporate Controller. ...

We are seeking a Senior Clinical Scientist to join our Oncology Clinical Science team. The successful candidate will be responsible for developing and executing clinical trials, working closely with cross-functional teams, and collaborating with external experts. The ideal candid ...

We are seeking a Senior Clinical Scientist to join our Oncology Clinical Science team. The successful candidate will be responsible for leading clinical trials and developing strategies for the development of new oncology drugs. The role requires strong communication and collabor ...

We are looking for a skilled Senior Accountant for a well-known real estate company. This role involves managing financial tasks for a major commercial trust in Asia. You should have strong analytical skills and a good understanding of IFRS and JGAAP standards. This position prov ...

Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. · ...

The job involves regulatory affairs and quality assurance work for biopharmaceuticals including applications, document creation, and coordination. · Responsibilities include pharmaceutical applications, authority interactions, CTD and FD document creation, new product introductio ...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. · p苦情担当スペシャリスト · tough punishment specialist · safety management department member performing following duties: kakujou shori: customer complai ...

Principal Safety Evaluation is responsible for ensuring the safety of products and patients throughout the product lifecycle. This includes conducting cross-functional activities to support the development of GSK Japan's projects, designing and implementing safety plans for clini ...

Our client seeks a Conference & Events Manager in central Tokyo for seamless meeting/event execution. · ...