Are you interested in contributing to Corporate and Investment Banking (CIB) from regulatory perspectives? As a Regulatory Reporting Operations - Associate within Market Operations, you will be responsible for 1.automation and regulatory/business/market initiated changes on Legal Ledgers and Regulatory reports owned
This is what you will do: Associate Director, Regulatory Affairs is responsible for overall pharmaceutical affairs associated with obtaining pharmaceutical product approval. The duties include complying with Japan pharmaceutical affairs act, developing good relations with the regulatory authority, and
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical
■ 職務内容 / Job Description Monitor is responsible to ensure that the trial is conducted and documented properly by carrying out the following activities when relevant and necessary to the trial and the trial site in
To support the growth of a global space startup, the Finance Associate plays a crucial role in devising and executing financial strategies such as fundraising, regulatory compliance and timely disclosures. The role will play a vital role in
Lead regulatory submission process, to contribute expansion of business. Maintain of product registration and related lincenses like MAH or manufacturing site through change control process. Requires basic knowledge of IVD/MD regulation and QMS. Will also cover regulations
At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world’s most complex health
BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Company Description Santen is a specialized life sciences company with a proud 130-year heritage focused exclusively on ophthalmology. As a Japan-originated, global company with our footprint in over 60 countries, we are dedicated to delivering innovative
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical
Be part of a critical member in the RA organization. Lead in RA development/strategy activities to obtain product approval for various unmet medical needs. Client Details * Global leading pharmaceutical business specialising in womens health *
職種 正社員 職務明細 Tokyo-based Langley Esquire is a public affairs consulting firm specializing in government relations, strategic communications, and public policy. We overcome challenges at the nexus of government, industry, and society. With over 30 years
We are seeking a Legal Entity Controller as a team member who will be involved in local regulatory reporting as well as monthly closing processes. As a Legal Entity Controller - Associate within the Legal Entity Control team,
Your days will be filled analyzing data and building models to assist clients from across the sector in best research firm. As a junior analyst in equity research team, you will be working in a dynamic
Blackstone is the world’s largest alternative asset manager. We seek to create positive economic impact and long-term value for our investors, the companies we invest in, and the communities in which we work. We do this
Job Description Summary プロジェクト並びに新製品にかかわる従業員の安全と健康、環境を管理する役割です。HSE戦略および活動を推進し、一貫した持続的な生産性とHSEの継続的な改善を達成する責任をチーム一丸となって担います。専門知識と積極的なサポートを提供することで、HSEの標準化、簡素化、業務への統合を確実にします。またHSEの短期および長期戦略がサイトの目標に合致していることを確認し、その実施を可能にします。 Job Description 主な役割責任 新ビジネスにおけるHSE要件の完全な実施のために、適切なリソースと予算が利用可能であることを確認する。すべてのHSE規制要求事項およびその他外部からの要求事項へのコンプライアンスを実証・検証するためのシステムが整っていることを確認する。 HSEマネジメントシステムマニュアル、GOP、クラスター／サイトSOP、および支援プログラムへの適合性を確保する。ノバルティスのHSE適合性レビューや法令遵守監査、検査、地方自治体からの訪問をサポートする。 HSEリソース、プロセス、手順、プログラムの配備における効率化と標準化を推進し、価値を創造する。 現場での総合的な検査、点検、安全ウォークのプログラムの実施を推進する。プログラムを実施するための適切なアカウンタビリティを確保する。 グローバル／プラットフォーム／クラスター／サイトのHSEチーム、委員会、タスクフォースに参加する。HSE問題およびプログラムに関して、他のクラスター、サイト、機能、および／またはグローバル・エキスパート・チームとのネットワークを構築し、連携する。 必須要件 物事の本質を見極め、論理的な思考で業務を遂行することに長けている事 学歴不問 工場での製造、オペレーション、サプライチェーン環境でHSE経験をお持ちである事（３年以上が好ましい） 日本語が流暢であること。英語での読み書きが可能（翻訳ソフト使用可能）で、将来的な英語力の向上に強い意欲をお持ちの方 HSEの経験をお持ちであれば望ましい（業界問わず） About the role: The role manages the safety, health and environment of employees involved in projects and new
Job Description The Goldman Sachs Group, Inc. is a leading global investment banking, securities and investment management firm that provides a wide range of financial services to a substantial and diversified client base that includes corporations,
Are you looking for an unique opportunity to advance your in depth knowledge of asset management and contribute to a growing international business in a fast paced and innovative environment? This is the right role for
Job Description The position takes a responsibility for medical contents in all clinical development programs in assigned therapeutic areas (such as dementia, movement disorders, neuromuscular, and MS/Immunology etc.) in Japan. The individual functions as a scientific
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical
