グローバル整形外科メーカーにて、RA Specialist/Sr Specialistを採用します。 · ...

グローバル整形外科メーカーにて、RA Specialist/Sr Specialistを採用します。業務拡大による増員募集で、今後 5年では様々な新プロダクトのリリースを控えております。大手整形外科プロダクトメーカーと肩を並べる成長企業で、チャレンジングなRA業務でキャリアアップしませんか? · ...

ヘルスケア業界のリーディングカンパニーであるビー・ブラウンエースクラップは、薬事担当としてのスキルと経験を尊重し、新たな目標に向かって飛躍することを共に応援します。私たちと一緒に次のステップを踏み出し、ヘルスケアの明るい未来を形作りませんか? · ...

Gilead is seeking a Therapeutic Specialist- RA to promote the commercial sales strategy for Jyseleca in Japan. The ideal candidate will have experience in immunology and be able to work effectively in a team environment. · Promote Jyseleca to healthcare professionals for RA patie ...

+QIAGENは、「生活の向上を可能にする」というシンプルで力強いビジョンを原動力としています。私たちは科学とヘルスケアをより良く変革することに専念しています。起業家としてのルーツから現在のグローバルなプレゼンスに至るまで、私たちは前向きな変化をもたらす力へと成長してきました。 · +Develops and prepares Japan Regulatory Strategy for QIAGEN product portfolio in partnership with RA Manager · Provides critical support f ...

We're creating a healthier world for all people. · Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for th ...

At Gilead we're creating a healthier world for all people For more than 35 years we've tackled diseases such as HIV viral hepatitis COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe We ...

+Job title: · Sr Sr Specialist RA · +Ensures rapid approvals for respective product lines by planning all registrations. · Interacts with regulatory agency personnel to expedite approval of pending registration.Provides management team with regular updates on product registration ...

The Regulatory Affairs Specialist supports global regulatory compliance for in vitro diagnostic (IVD) products ensuring timely market access and adherence to international standards. · This role encompasses product registration launch change management and other regulatory activi ...

+p>The Regulatory Affairs Specialist supports global regulatory compliance for diagnostic products where the company acts as the Legal Manufacturer ensuring timely market access and adherence to international standards. · +/p+Prepare submit and track regulatory applications · Ev ...

The Regulatory Affairs Senior Specialist shall contribute and lead the Regulatory Affairs for the CooperVision Japan business. · ...

The PV Senior Specialist collaborates with colleagues to ensure compliance with local laws and regulations. They are responsible for all PV activities and may serve as the PV contact with local stakeholders. · Serves as the back-up PV Responsible person/QPPV as required per local ...

Join us, and together, we'll transform our industry, making a lasting difference for brighter lives and a better world. You light the way. · Joint accountability with the BP for the integrity, consistency and completeness of the P&L and Balance sheet of the allocated ORUs at tota ...

As a Finance Controller, you will be responsible for the Far East region, including Japan and Korea. You will work intensively with a broad set of colleagues from different levels, expertise, and geographic location. You will be part of the accounting organization in Growth Marke ...

The Regulatory CMC Expert evaluates all CMC regulatory aspects related to the assigned products (including both development products and established products) in Japan. · The Regulatory CMC Expert develops and executes CMC strategies for development products/life-cycle management ...

As a Finance Controller in the Growth Markets organization at Signify in Tokyo Japan you will be responsible for the Far East region including Japan and Korea. · ...

This position offers a unique opportunity for growth with an international cosmetics manufacturer expanding into Japan. · The role involves managing compliance systems for pharmaceuticals , quasi-drugs ,and cosmetics . · ...

+ 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 Regulatory CMC Expert evaluates all CMC regulatory aspects related to the assigned products (including both development products and established products) in Japan. · Evaluates the available technical and scientific CMC information for compliance with regulatory requirements, ...

You will be mainly responsible for Far East region which includes Japan, Korea. Joint accountability with the BP for the integrity, consistency and completeness of the P&L and Balance sheet of the allocated ORUs at total and at MRU level. · You will be mainly responsible for Far ...

We are looking for an experienced Interim Financial Controller to support our Finance team during a critical period: the FY2025 year-end closing, the preparation of the IFRS Annual Report, · a ndthe first external audit with our new auditor KPMG.A strong finance professional with ...