About Johnson & Johnson At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive,
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Job Description: This is an exciting important managing role of Ferring Pharmaceutical to have the following GQP and QMS activities Roles supervising by GQP quality responsible person (Hinseki) and head, Quality Management as well as leading Ferring
Overview We are currently seeking an Informatics Professional Service (IPS) Specialist who will provide high level consultation support to customers in the area of informatics, including Enterprise systems and chromatography data systems (CDS). Responsibilities Actively be
企業概要 Santenは、眼科医療に特化した130年の歴史を持つ製薬企業です。日本発のグローバル企業として60カ国以上に拠点を持ち、目の健康のために様々な革新的な治療法とデジタルソリューションを提供し、世界中の人々の視覚に関わる社会問題に取り組んでいます。 Digital & Information Technology(D&IT)本部は各リージョンに展開し、一つのチームとしてグローバルに展開するSantenビジネスオペレーションとプロセスの変革推進を技術的側面から力強く支えています。 特にHead of Digital Strategy & InnovationのポジションはSantenのデジタルトランスフォーメーションをグローバルにリードし、デジタルを活用し組織を変革していく上で重要且つエキサイティングな役割です。 求人内容 Position Purpose Under the direction of the Global Head of DIT/Digital & Information Technology, lead Santen’s digital transformation globally by developing plans to
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring
Job Description SummaryAs a CMC development specialist, enhance Japan’s CMC development strategy by offering scientific and technical support to global/local CMC development teams and other departments, while keeping up with the latest technological advancements. [Note] 1:
Job Purpose & Key Responsibilities ViiV JLTメンバーの一人として、コンプライアンス以外も含めて多くの経営課題に対する議論や意思決定へ参加します。 コンプライアンスの観点から「できる／できない」を判断するのが重要ですが、「できない」場合にどうすれば「できる」ようになるのかを考えてビジネスオーナーに助言します。（Enablerとしての役割と責任を求められます。） ViiV Japanではただ一人のコンプライアンス担当なので、全部門からコンプライアンスに関する質問や相談を受けます。そのため、販売情報提供活動ガイドライン、公正競争規約、製薬協コード・オブ・プラクティス、Corporate Policies（Authored by ViiV/Adopted from GSK）等の幅広い理解が必要となります。 製薬協の透明性ガイドラインに基づく情報開示に関して準備業務をリードします。 The key responsibilities will include but are not limited to the following main areas: Ensure effective implementation of a value-based
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
Are you passionate about driving strategy in talent management? Do you thrive in a strategic role, working closely with executive team members and global colleagues? If so, we have an exciting opportunity for you to join
Job Description Summary-This is a universal job description meant to capture some of the primary duties of this role that are common across functions or divisions. It is not intended to represent all of the specific
Regulatory Affairs Manager CH Japan YOUR TASKS AND RESPONSIBILITIES: Determine local regulatory strategies and manage operational tasks to fulfill the local business strategies for the CH portfolio, in coordination with local functions and with close coordination
Are you an experienced Engineering Supporter looking for a new challenge? Do you thrive in a cross-functional environment and enjoy implementing innovative solutions? If so, we have an exciting opportunity for you to join our team
Job Description This role is responsible for Japan regulatory expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsibilities include Japanese registered information dossier
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
Job Description Job Description Menuma DMO Lead – Scope Summary: The Menuma Digital Manufacturing Operations (DMO) Lead is responsible for ensuring all DMO capabilities are effectively implemented, operationalized, and sustained in Menuma (Japan) manufacturing site. This scope currently
Department:Regulatory CMC Japan Report to:Head,Non-clinical & CMC Dev 1. Act as a key person to coordinate CMC and/or regulatory science issues between global and Japan so that appropriate solutions are provided 2. Be responsible for preparation
Job Description 1. Quality Management of third-party manufacturers and suppliers 2. Quality Operations of EM CHC JAPAN Entity 3. Quality Training 4. Quality Technical Support The EM CHC JAPAN Senior Quality Manager (EM CHC JAPAN -
JOB description To keep up and improve the local supply processes in Japan including roles and responsibilities of involved local and global functions as well as the SOP system which should be in line with global
Project Manager/ BioReliance® Contract Testing Services, Life Science Services Location: Tokyo Report to: Manager in Japan Direct report: 0 ABOUT BioReliance® Contract Testing Services BioReliance® Testing Services provides testing and manufacturing services to pharmaceutical and biopharmaceutical companies that
