Compliance and Regulations Jobs in Japan

DescriptionChange the world. Love your job.The Field Applications Engineer Processor (FAEP) is responsible for partnering with Sales and providing Processor related technical expertise throughout the sales cycle. The FAEP proactively identifies current products and/or creative solutions to solve exi...

JOB DESCRIPTION:MAIN PURPOSE OF THE ROLEIndividual contributor representing the most common entry point for this career stream.Works under direct supervision.MAIN RESPONSIBILITIES Identifies and validates molecular targets that play a key role in a particular disease process. Studies origin relati...

DescriptionChange the world. Love your job.The Field Application Engineer Processor (FAEP) is responsible for growth of Processor products revenue as a part of the sales team by partnering with Sales and Analog FAE. The FAEP proactively promotes TIs competitive devices and solutions by providing cre...

職務内容 / Job DescriptionClinical Scientist (CS) is a clinical project lead with strong experience in multidisciplinary aspects of drug development and is accountable/responsible for generating clinical development strategy designing clinical development options and delivering successful clinical...

職務内容 / Job DescriptionClinical Site Lead (CSL) is a field-based role within Site Management & Monitoring (SMM) at AstraZeneca K.K. dedicated to supporting clinical trials within Japan. The CSL will be assigned to dedicated disease area and proactively drive site performance enhance site engagem...

Job DescriptionAs the independent second line assurance function for R&D our mission in Quality Assurance is to achieve enduring excellence in auditing quality management quality risk assessment and enhance the R&D quality mindset for the benefit of our patients.The job holder is responsible for one...

職務内容 / Job DescriptionAssociate Director Clinical Quality Management (ADCQM) leads the planning and implementation of all quality activities adapting to changes in the environment through relevant Clinical Quality Management System. ADCQM is individual contributor and skill expert which meets o...

職務内容Description: The PS Epidemiologist (PSEPI) serves as a study lead for Post Authorization Regulatory Commitment Studies (PARCS) including post-marketing database study and use-result survey accelerating the generation of valuable real-world evidence. Leveraging extensive clinical research exp...

Role DescriptionThe Personal Assistant to the Head of R&D Japan is responsible for performing a wide range of high impact executive administrative and project-oriented activities in direct support of the Head of R&D Japan and the R&D Japan leadership team. The role involves initiating and managing e...

職務内容 職務内容 / Job Description呼吸器領域の医療施設医師薬剤師に対する医薬品の情報提供活動および適正使用の推進 応募資格(経験資格等) / Qualification (Experience & Skill etc.)Typical AccountabilitiesEducation Qualifications Skills and Experiencee必須 / Mandatory

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About the roleWe are looking for a Head of Regulatory Affairs who is strategic collaborative and peoplefocused to join our Regulatory Affairs team based in our Nishi-Shinjuku office in Tokyo Japan.You will lead the regulatory str...

Are you passionate about streamlining processes and creating impactful procedural documents Join our Global Development team as an Operations Manager Process & Procedures where youll drive the development and management of our controlled procedural document portfolio. This role offers the opportunit...

Are you passionate about streamlining processes and creating impactful procedural documents Join our Global Development team as an Operations Manager Process & Procedures where youll drive the development and management of our controlled procedural document portfolio. This role offers the opportunit...

Job SummaryAre you passionate about advancing health and wellness through innovative bioscience solutionsIFF is a global leader in flavors fragrances food ingredients and health & biosciences. We deliver sustainable innovations that elevate everyday products.Health & Biosciences (H&B) is dedicated t...

Work Flexibility: Hybrid or OnsiteThe Jobs MissionUnder minimum supervision by Manager he/she understands the related laws and regulations and efficiently conducts the duties such approval applications notifications and other related tasks.マネジャーの最小の指導の下薬機法全般に精通し豊富な知識と経験...

Career CategoryQualityJob DescriptionThe Senior Manager of Quality Assurance at Amgen leads the QA department and plays a crucial role in establishing implementing and maintaining the Quality Management System. They ensure the organizations compliance with regulatory standards and drive continuous i...

Position PurposeThis role drives strategic pricing decisions that accelerate patient access to Pfizers products and safeguard business value while shaping pro-innovation pricing frameworks with the Ministry of Health Labor and Welfare (MHLW) and industry stakeholders.ResponsibilitiesDevelop and exec...

Job Description業務内容1. グローバル戦略に沿った効率的かつ付加価値の高い新薬等の国内開発薬事戦略の構築2. 規制当局厚生労働省独立行政法人医薬品医療機器 総合機構などとの窓口業務3. 承認申請審査資料機構相談資料照会事項に対する回答等へのレビューアドバイスを通じ当局提出文書の質の向上に資する4. 承認申請審査...

ROLE SUMMARYThe Sr. Manager/Staff Engineer AI Infrastructure & MLOps Engineering is a senior technical leader responsible for architecting building and scaling Pfizers AI infrastructure and developer platforms. This role leverages extensive experience in cloud engineering DevOps and MLOps to deliver...

職務概要臨床試験のデザイン分析解釈を関連する薬事規制要件標準業務手順書SOPおよびベストプラクティスに従って業務を行う臨床開発チームの中で特に臨床開発リーダー臨床薬理担当者統計担当者で効果的に協働し科学に基づいた統計の専門知識を生かし医薬品開発に貢献する職務内容試験デザイン統計解析計画統計解析結果の解...