医薬品製造の一端を担うことで、病気の治療や生命維持などにおいて社会へ貢献します。ものづくりを通して製造品目が出来上がった時の達成感は格別です。 · 有機化合物/原薬(医薬品の原料)や化成品等を製造している千葉工場製造部・製造チームの一員としてご活躍いただきます。 · ...

The Narita Plant is primarily involved in manufacturing plasma-derived therapies that save lives and provide trusted plasma-derived treatments. The plant has a comprehensive production process involving raw materials (plasma fractions), finished product manufacturing, inspection/ ...

+We are looking for an Operator at our Narita site to join our team. · + · Perform visual inspection of biologics products. · Packaging and labeling of biologics products. · ...

The job requires native level Japanese language command in speaking, business writing and reading. The employee will be responsible for manufacturing plasma-derived medicinal products and managing the production equipment. The Narita Plant is mainly involved in the manufacture of ...

Medical Catalog Specialist supports sales of pharmaceuticals at Amazon's dedicated logistics center for pharmaceuticals while maintaining compliance with Pharmaceutical Affairs Law. · ...

This role supports sales of pharmaceuticals in accordance with the Pharmaceutical Affairs Law at Amazon's dedicated pharmaceutical logistics center. The position contributes to business expansion by expanding product selection support for business teams as well as supporting phar ...

Quipment is a fast-growing company at the forefront of innovation in the medical device sector for global clinical trials. As part of our continued growth at our Technical Center in the Chiba Region, Japan we are seeking a Sales Assistant to join our Sales team in this role you w ...

Medical catalog specialist supports sales of pharmaceuticals by Amazon's pharmacy logistics center while maintaining compliance with the Pharmaceutical Law. · The role involves expanding business through selection expansion, supporting business teams, · and providing pharmacist o ...

We are seeking a Sales Assistant to join our Sales team in Chiba Region, Japan. · Collaborate with the Sales Representatives on creating quotations. · Assist the Sales Representatives in the quotations checking process. · Understand the customer's needs and identify the right pro ...

A leading medical device/pharmaceutical company in the US with a rich welfare system seeks a Medical Affairs Manager based in Tokyo. · Building Clinical evidence · Identify clinical trial needs based on clinical strategy · Negotiate with KOL and cooperate with internal and exte ...

The company is seeking a Quality Assurance Technical Service Specialist to handle the following responsibilities: Product-related collaboration with manufacturing contractors · Technical transfer and maintenance management of products · This role requires experience in CMC-relate ...

We are seeking a Quality Assurance Technical Service Specialist to join our team in Tokyo. The successful candidate will have experience in CMC-related business, including product collaboration, technology transfer, and maintenance management. · ...

We aim to prevent stop and cure diseases ensure everyone has access to healthcare today generations come. · ...

We're looking for a Principal Specialist to join our QARA team in Tokyo. As a General Marketing Supervisor under the PMD Act, you'll ensure compliance with all applicable QMS and GVP requirements. · ...

We are seeking a Quality Assurance/Control Specialist to join our team at Boehringer Ingelheim Corporate. As a key member of our quality assurance team, you will play a crucial role in ensuring high-quality products reach customers safely and effectively. · You will be responsibl ...

Finance & HR Generalist to contribute to the company's growth in Tokyo. · Handle daily and month-end accounting activities and prepare profit & loss statements and Balance Sheet. · Manage treasury, including control of vendor invoice and employee expense, payment execution, and p ...

Telix Pharmaceuticals seeks Quality Manager to oversee manufacturing quality control management at its Japanese facilities. This role ensures compliance with Japanese regulatory requirements (PMDA Ministry of Health Labour Welfare JNMT) The main responsibilities include: GMP(適正製造 ...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access equity all. · ...

The Quality Manager will support the international roll-out of our approved prostate cancer imaging agent and help advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. · ...

+ 10 years' practical experience with CMC-related roles preferred (CMC regulatory affairs, Analytical/Quality testing, or Manufacturing) in Pharma Industry Advanced degree in medical, pharmaceutical or life-science etc Hard skills/ Expertise: Idealy + 10 years' practical experien ...

The main responsibilities of this role include ensuring compliance with GQP Ordinance regulations by creating SOPs for drug products. · ...