Johnson & Johnson is the worlds most comprehensive and broadly-based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in pharmaceutical, and medical devices and
Company Description Block is one company built from many blocks, all united by the same purpose of economic empowerment. The blocks that form our foundational teams — People, Finance, Counsel, Hardware, Information Security, Platform Infrastructure Engineering,
The Role: Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, youll be
About ERM: Sustainabilityis our business. As the largest global pure play sustainability consultancy, ERM partners with the world’s leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today
■ 職務内容 / Job Description Medical Communication Scientist (MCS) is a role name in AZKK and is generally known as medical writer. MCS is responsible for the authoring of clinical-regulatory documents and submission packages that communicate the
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
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
職位記述書 職務名 薬事規制スタッフ 勤務地 東京本社 レポート先 Quality, Safety & Regulatory Manager 担当ディビジョン Consumer Beauty & Luxury /Rimmel, Gucci, Burberry, CK, Tiffany,etc. 雇用形態 正社員 (full time) 業務内容 化粧品製造販売業者コティジャパンの薬事業務の遂行 主要業務 (70%) コティジャパン薬事規制業務 マーケティングおよび R&D と協力し、製品の成分、製品訴求、および製品表示が日本の規制に適合している事の確認 化粧品の申請書類作成・申請業務 化粧品の届出業務 (30%) 安全管理責任者（安責）業務
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your
At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your
You are a team contributor who enjoys working collaboratively Opportunity to innovate and drive pioneering business initiatives Together we can drive sustainable business growth for our clients Do work that matters: We’re undergoing a rapid transformation,
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
Title: Regulatory Affairs Manager Company: IPSEN K.K. Job Description: Ipsen is a dynamic and growing global specialty-driven biopharmaceutical company focused on innovation and specialty care. We aim to make a sustainable difference by significantly improving patients’ health
If you have what it takes to become part of the Vistra family and would like to start a promising career with a global leader, take a look at the exciting employment opportunities that are currently
Minimum qualifications: Bachelor’s degree in Business/Business Law, Human Resources, a related field, or equivalent practical experience. 5 years of experience in labor relations, industrial relations, employee relations, and labor law. Ability to communicate in Japanese and
Title: Medical Advisor / Medical Scientific Liaison FOP Company: IPSEN K.K. Job Description: As part of the Medical Affairs department, the MA/MSL is a hybrid, field-based scientific expert to external and internal stakeholders delivering non-promotional information
Req ID 64147 | Miyoshi, Japan, ZF Japan Co., Ltd. What you can look forward as Plant Quality Control Manager: Develop, implement, and maintain the plants quality management system (QMS) in alignment with corporate quality policies.
Job Description Summary -Provide timely & professional ongoing Mgmt of Data Mgmt/Coding/CDDRA-Database Development/DAP deliverables and of clinical trial data with respect to cost, quality and timelines for all assigned trials within Clinical Data Mgmt. Ensure consistently
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
