Drug Safety Associate - Tokyo Osaka - Office Hybrid ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility,
MAIN REPONSIBILITIES / DUTIES JOB POSITION PURPOSE The MAS role family comprises a variety of medical scientific specialties, such as BU Medical and field based Medical. Be the Pfizer Japan medical scientific point of contact for
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON)
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Role Summary The clinician contributes towards providing medical and scientific expertise and oversight for Clinical Trials conducted worldwide with a primary focus in Japan and the Asia-Pacific region. The clinician may be required to design a
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企業概要 About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples
JOB SUMMARY The HR Manager directs and works with Human Resources and Operations employees to carry out the daily activities of the Human Resource Office including oversight of recruitment, total compensation, training and development, association/labor relations,
POSITION SUMMARY Applicants should have a valid work visa for Japan or be eligible to work in Japan. Assists in carrying out the daily activities of the Human Resource Office including recruitment, total compensation, and training
Make your mark for patients 患者さんのためにあなたの力を発揮してください 概要 埼玉工場で製造し、日本市場へ出荷する医薬品の品質を保証するポジションです。国内規制、医薬品業界のガイドライン、社内品質基準に基づき、品質システムの構築・維持・改善を担います。部下を持たない専門職(Individual Contributor)としてプロジェクトや品質改善をリードいただくポジションです。 主な業務内容 1. 品質保証(Quality Assurance) ・日本市場へ高品質な製品を安定的かつ継続的に供給する ・埼玉工場における品質システムの構築・維持・改善を推進する ・品質システムが日本の規制当局要件、製薬業界関連ガイドライン、およびUCBの品質方針・品質基準に適合していることを保証する ・担当領域における各種KPI目標の達成に貢献する 2. メンバー支援・育成(Support and Training) ・埼玉工場全体および担当領域における品質保証活動を推進し、高品質な製品の安定供給と品質目標の達成に貢献する ・担当領域のメンバーに対し、GMP教育や品質保証に関する指導・育成を行い、組織全体の品質文化向上を支援する 3. 継続的改善(Continuous Improvement) ・オペレーショナルエクセレンス(OE)活動に参画し、埼玉サイトにおける品質および生産性の向上を推進する 4. HSE(Health, Safety & Environment) ・HSE活動を推進し、自身およびチームメンバーの安全・健康を確保する ・環境負荷の低減に向けた取り組みを実施する ポジションの魅力 ・グローバル企業の品質システムに触れながら、低分子医薬品の品質保証領域で専門性を高められる環境です。 ・埼玉工場では低分子医薬品を取り扱っており、品質システムの運用から改善活動まで幅広く携わることができます。
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, andsolutions are personal.Through our