26 Quality Assurance And Engineering jobs in Tokyo.

Tokyo

• Skills: regulatory submissions, MHLW, PMDA, JNDA, post-marketing maintenance, drug registrations, biotechnology, pharmaceuticals, clinical development, Japanese regulatory environment
• Level: senior
• Type: full_time

Tokyo

• Skills: Quality Assurance, GMP, biopharmaceutical, Quality Systems, Regulatory Affairs, project management, risk management, cold chain products, partner oversight, compliance
• Level: senior
• Type: full_time

Tokyo

• Skills: Quality Assurance, Good Manufacturing Practice, Quality Control, Regulatory Affairs, Supply Chain Management, Quality Systems, Risk Management, Cold Chain Products, GMP Compliance, Pharmaceutical Regulations
• Level: senior
• Type: full_time

Tokyo

• Skills: Customer Success, Life Sciences, Quality Cloud, SaaS, Document Management, Consultative Role, Stakeholder Management, Software Implementation, Problem Solving, Product Feedback
• Level: mid
• Type: full_time

Tokyo

• Skills: Pharmacovigilance, Safety information, Risk management, Local Qualified Person, Aggregate Reports, Regulatory compliance, Signal detection, Quality system, Self-inspection, Leadership
• Level: mid
• Type: full_time

Tokyo

• Skills: Quality Management, GVP, Regulatory Affairs, Post-marketing Surveillance, Complaint Handling, SOP Development, Medical Device Safety, MHLW Communication, Documentation Management, Cross-functional Collaboration
• Level: mid
• Type: full_time

Tokyo

• Skills: SAP, Quality Management, GxP, Compliance, Pharma, Life Sciences, Configuration, Business Process Mapping, Training, Cross-functional Teams
• Level: senior
• Type: full_time

Tokyo

• Skills: ICSR management, Pharmacovigilance, Medical Information, Regulatory Affairs, Quality Assurance, Case Processing, SAE/SUSAR Management, MedDRA coding, Data protection, Workflow management
• Level: mid
• Type: full_time

Tokyo

• Skills: Regulatory Affairs, Biopharmaceutical, Clinical Trials, Drug Development, Project Management, Regulatory Consulting, CRO, Clinical Research, Patient Care, Emerging Talent
• Level: senior
• Type: full_time

Tokyo

• Skills: Regulatory Affairs, Oncology, Rare Disease, Regulatory Strategy, Compliance, Filing Plans, Product Development, Stakeholder Engagement, Japan Regulatory, Clinical Projects
• Level: mid
• Type: full_time

Tokyo

• Skills: regulatory submissions, medical device industry, MDSAP, compliance activities, project management, FDA, technical files, document review, change control, team leadership
• Level: mid
• Type: full_time

Tokyo

• Skills: Project Management, Product Safety, UL Standards, Client Communication, Testing and Inspection, Technical Assistance, Compliance, Quality Assurance, Engineering, Research and Development
• Level: senior
• Type: full_time

Tokyo

• Skills: GCP, 監査, 医療機器, 臨床試験, コンプライアンス, 教育・指導, プロセス改善, CAPAレビュー, 品質管理, 国内外法規制
• Level: mid
• Type: full_time

Tokyo

• Skills: ICSR Management, Pharmacovigilance, Quality Assurance, Medical Information, Regulatory Affairs, Line Management, Team Efficiency, Project Management, Client Cooperation, Training
• Level: mid
• Type: full_time

Tokyo

• Skills: medical writing, clinical development, biopharmaceutical, regulatory affairs, project management, data analytics, clinical trials, patient safety, pharmacovigilance, cross-functional collaboration
• Level: entry
• Type: full_time

Tokyo

• Skills: regulatory affairs, CMC, NDA, PCA, regulatory evaluation, change control, submission documents, PMDA, quality assurance, project development
• Level: senior
• Type: full_time

Tokyo

• Skills: Quality Management System, GCP, KPIs, Quality metrics, Regulatory compliance, Process Quality, Corrective action, Risk assessment, Data analysis, Project management
• Level: mid
• Type: full_time

Tokyo

• Skills: regulatory strategy, global licenses, regulatory dossiers, health authority communications, drug regulatory activities, medical devices, regulatory submissions, project management, negotiation, problem solving
• Level: senior
• Type: full_time

Tokyo

• Skills: project management, clinical trials, GCP, ICH, SOPs, risk management, biopharmaceuticals, regulatory compliance, clinical development, clinical research
• Level: mid
• Type: full_time

Tokyo

• Skills: Regulatory Compliance, Auditing, International Regulations, FDA, EMA, ISO Standards, Risk Assessment, Analytical Skills, Communication, Report Writing
• Level: senior
• Type: full_time