今回は、企業規模の拡大に伴い、医薬品製造管理者(薬剤師)を募集します。 · 《主な業務内容》 · 注:すべてを担うということではございません。スキル等によって担当業務は変わります。 · ...

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 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 ...

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

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/ ...

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 ...

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 ...

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

Perform GXP activities according to GQP/GMP Ministerial Ordinance and GDP guideline. · SUPVISE DOCUMENT CONTROL DEFINED IN GQP ORDINANCE · ...

We are a company engaged in the manufacturing sales import and export of pharmaceuticals and quasi drugs. Guided by our philosophy of enhancing peoples health and contributing to a richer society we focus on the introduction and development of innovative new drugs particularly an ...

+Job summary · The GXP Quality Assurance Specialist will oversee all aspects of quality assurance in accordance with regulatory requirements. · +ResponsibilitiesSUPervise document control defined in GQP Ordinance (SOP Quality Standard Codes) · ...

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. · ...

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 ...

This position involves overseeing GQP activities in accordance with GQP Ordinance and GDP guidelines. · Supervise document control defined in GQP Ordinance (SOPs) · Release products to the market ensuring proper manufacturing control and quality control · Achieve proper manufactu ...

+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. · ...

Are you ready to accelerate your potential and make a real difference within life sciences, · diagnostics and biotechnology? · ...

+ 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 ...

This position plays a pivotal role at one of the world's leading biopharmaceutical contract manufacturing business organizations contributing directly to shaping the future of biotechnology and biopharmaceutical industry as Director of Business Development & Key Account Managemen ...

This role plays a pivotal part at one of the world's leading biopharmaceutical contract manufacturing business organizations contributing directly to shaping future biotechnology. · Execute contract manufacturing business strategy with focus on mammalian & microbial technologies ...

We are engaged in the research, development and provision of medical technologies in Japan. In particular, we focus on the development of innovative therapies and provide advanced technologies related to cancer treatment. · 医療機器の設計検討、試作・検証、製品化に向けた開発業務全般 · 技術課題の抽出および、改良または新たな解決策の検 ...