Daiichi Sankyo Company,limited jobs

Director, Early Phase Biostatistics Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary Position leads multiple early phase compounds or complex studies contributing to clinical development plan, and responsible for statistical design, analysis and interpretation of results independently with minimal supervision. This position provides strategic inputs to entire drug development plans with minimal supervision and regulatory responses and other documents with minimal supervision. This position interacts with global project teams and global Health Authorities, as well as contract research organization (CRO) programmers and statisticians. Additionally, this position works under minimal supervision to solve complex project problems. This position utilizes innovative trial designs and modeling to optimize the statistical handling in the projects, in collaboration with statistical innovation group, precision medicine biostat group, and real-world data (RWD) group. This position collaborates with cross fu

Manager (m/w/d) MAH QA Compliance Work Model Office Based Role (Daiichi Sankyo Europe) | Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Purpose of the function Ab sofort suchen wir für unseren Standort in Pfaffenhofen oder München eine/n engagierte/n Manager (m/w/d) MAH QA Compliance Manager Angaben zur Tätigkeit: Als Manager (m/w/d) MAH QA Compliance unterstützen Sie die Abteilung umfassend bei allen qualitätssicherungsrelevanten QA-Aktivitäten. Sie fungieren als zentrale Schnittstelle zwischen internen Fachbereichen und externen Partnern, gewährleisten eine vollständige und sorgfältige Vorbereitung für die finale Freigabe und übernehmen bei Bedarf die fachliche Anleitung von Teammitgliedern. Zudem arbeiten Sie eng mit der Abteilungsleitung zusammen und konzentrieren sich dabei besonders auf folgende Kernbereiche: Koordination und Durchführung des Marketing Authorization Holder (MAH) Reviews für Product Quality Reviews (PQRs) gemäß regulatorischen Anforderungen (EU-GMP, ICH Q7/Q10 und des EMA reflection papers on GMP and MAHs) Fristgerechte Kollektion alle

Senior Manager, Biostatistics (Late Stage) (m/w/d) Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. The Position: Position leads complex studies in study design, statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision. This position also guides contract research organization (CRO) programmers and statisticians in preparing analysis files and performing statistical analyses. Additionally, this position interacts with study teams, as well as statisticians and programmers at CROs. This position works under some supervision to solve complex study problems. Roles and Responsibilities: Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, prot

Senior Associate, Global Oncology Medical Affairs, External Scientific Collaboration Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary The Senior Associate, External Scientific Collaboration plays an important role in enabling the effectiveness and therapeutic focus of the External Scientific Collaboration team. This position is responsible for developing/improving tools and resources that facilitate efficient and effective external engagement processes, outputs and reporting. They manage the coordination and end-to-end processes that support medical engagement activities, including submission and tracking of materials through internal compliance and legal review, coordination of congress-related activities, and development and maintenance of key information sources. As a strategic partner within the team, they work with cross-functional leaders to optimize how our systems connect to drive efficiencies and identify mechanisms to accelerate team deliverables. A core responsibility of this role is to ensure compliant and efficient execution of co

Scientist (m/f/d) GMP ADC Manufacturing Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. For our development and production site in Pfaffenhofen an der Ilm we are seeking highly qualified candidates to fill the position: Scientist (m/f/d) GMP Manufacturing ADC The position: The Scientist GMP manufacturing ADC will be a key contributor to the establishment of a new drug substance production unit for Antibody-Drug Conjugates (ADC) at the site in Pfaffenhofen. Your primary role will be to support the establishment of the new production facility as expert from GMP perspective, including the generation of the required GMP documents. Once the facility is up and running, your task will be to contribute to all operations and maintenance in this GMP bioconjugation facility. You task will include to ensure performance of your tasks in compliance with the regulatory requirements and collaborating with other departments to support manufacturing with good quality. Roles and responsibilities: • Contribute to the planning of

Dir Clinical Operations Non-MD Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary Provides operational oversight to study management personnel within assigned program(s). Provides managerial oversight to colleagues that they are directly line managing in their group. They will ensure their direct reports are meeting required study deliverables including but not limited to oversight of CROs and Vendors and (as applicable) properly leading and ensuring delivery of milestones for the studies within assigned program(s). They are accountable to ensure their direct reports are delivering to agreed upon study plans, properly identifying risks/mitigations, escalating as appropriate and utilizing data and metrics to put appropriate strategies and plans in place as well as measuring the status/variance of a study and putting appropriate measures in place to course correct where needed. The Director will be accountable to support SDL and employee personal development, including routine talent management

Associate Director PV Quality, Americas Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary Participate in the implementation of the quality strategy closely aligned with the business strategy within the CSPV function. Provide strategic and proactive QA Leadership and support development Project Teams and CSPV with adequate quality and compliance guidance in close alignment with the Head of Global PV QA Americas. Including, daily consultation to CSPV unit to harmonize end to end "proactive quality". Advise development teams in quality and compliance decision making to drive sustainable quality and compliance excellence. Provide quality and compliance guidance for process deviations and implementation of corrective and preventive actions, including enhanced involvement on Root Cause Analysis (RCA); monitor their status and timely closure. Support risk management activities, including trend analysis KQIs (e.g. Audits, Inspections, QIs including late ICSR submission of reports, and their CAPAs, etc.) from

Director, Global Oncology Marketing, Omnichannel Strategist Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary The Global Omnichannel Content Strategist is responsible for defining and advancing a cohesive global content governance and modularization framework that enables scalable personalization and reuse across regions. This role establishes global standards, taxonomy principles, and governance models to support alignment, efficiency, and brand consistency, while regional omnichannel teams retain responsibility for content execution, localization, and deployment. This position operates as a strategic architect and cross-functional integrator, partnering with regional and content leads, platform owners, medical, and marketing stakeholders to enable adoption of global frameworks and continuous improvement in content lifecycle processes. Working closely with Global, US and EUCAN content leads and editorial teams, the Strategist will drive alignment and continuous improvement in global content governance, workflows, and p

Mitarbeiter (m/w/d) Wiegezentrale befristet auf 2 Jahre Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Angaben zur Tätigkeit Als Mitarbeiter (m/w/d) in der Wiegenzentrale stellen Sie die ordnungsgemäße Verwiegung und Bereitstellung von Rohstoffen für die Arzneimittelherstellung sicher. Sie führen die Verwiegung von Wirk- und Hilfsstoffen gemäß Herstellvorschriften, Arbeitsanweisungen und GMP-Richtlinien durch. Die Identitätsprüfung sowie die Kontrolle der bereitgestellten Materialien gehören ebenso zu Ihrem Verantwortungsbereich. Sie dokumentieren sämtliche Arbeitsschritte sorgfältig und GMP-konform in den entsprechenden Herstell- und Chargenunterlagen. Darüber hinaus sind Sie für die Reinigung und Pflege der eingesetzten Geräte, Waagen und Arbeitsbereiche verantwortlich. Sie unterstützen bei Bestandskontrollen sowie bei der Materialbereitstellung für die Produktion. Die Einhaltung von Hygiene-, Sicherheits-, Betriebs- und Umweltvorschriften ist für Sie selbstverständlich. Zudem wirken Sie aktiv an der kontinuierlichen Verbe

HCP Engagements Specialist Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary This position is responsible for overseeing the end-to-end contracting documentation and payment process for Healthcare Professionals (HCPs). This role will have sole responsibility of understanding, reviewing, and following all Programs and Grand Committee (PGC) HCP guidelines and regulations including, managing HCP contracting and HCP payment processing. This role will be the primary point of contact for all HCPs' communications and inquiries, including managing HCP interactions. This position requires the ability to apply independent judgment and critical thinking skills to address difficult issues that result in workable solutions. Job Description Responsibilities Exhibit a robust understanding, and critical thinking of compliance requisites and remain informed about policy and process updates. Ensure unwavering adherence to all Standard Operating Procedures (SOPs), internal policies, procedures, and corpora

Manager, Statistical Programming (m/f)d) Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. The Position The purpose of this role is to lead and contribute to statistical programming activities across SDTM, ADaM, and Tables, Listings, and Figures (TLFs), providing both technical oversight and hands-on support for the development, validation, and programmatic review of datasets and outputs. This role ensures the quality, consistency, and timeliness of deliverables supporting oncology regulatory submissions by guiding programming strategies, reviewing key outputs, and driving issue resolution. In addition, this position fosters and maintains institutional knowledge across oncology compounds, while supporting the development, standardization, and continuous improvement of programming processes and best practices for datasets and TLFs to enhance efficiency, quality, and compliance. Roles and Responsibilities Lead and Execute Statistical Programming Develop and validate datasets and Tables, Listings, and Figures (TLFs)

Sr Analyst Engagement Monitoring Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary This position is primarily responsible for monitoring / auditing HCP (Health Care Provider) activities for all engagements pertaining to their travel and/or attendance at meetings, speaker programs, and conventions as well as single engagements in support of DSI (commercial and development organizations). This role is also responsible for monitoring and auditing all non-HCP meetings and activities according to DSI policies. The role will have primary responsibility within Corporate Programs & Events for ensuring DSI's compliance with all CIA related policies, state and federal regulations regarding payments to HCPs and reporting of such for the listed activities. Job Description Responsibilities HCP Engagement folders - Establish and manage the monthly HCP Engagement Folder audit process, to ensure information is documented and reported timely. Folder Audit includes: Review HCP Engagements that are considered cl

Bioprocess Specialst (m/w/d) DSP Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Die Position: Ab sofort suchen wir für unseren Standort in Pfaffenhofen eine/n engagierte/n Bioprocess Specialst (m/w/d) DSP Angaben zur Tätigkeit: Zum aktuellen Zeitpunkt befindet sich das Projekt und die damit verbundenen Tätigkeiten in der Etablierungsphase: Etablierungsphase Sie sind verantwortlich für die Etablierung ausgewählter DSP-Prozessschritte mit Single Use Materialien, angefangen bei der unterstützenden Geräteinbetriebnahme und -qualifizierung (DQ/IQ/OQ) Planung und Umsetzung von Leistungsqualifizierungsaktivitäten (PQ, PPQ) Erstellung und Überprüfung von Risikoanalysen, Qualifizierungs- und weiteren GMP-Dokumenten Etablierung von GMP-gerechten Herstellanweisungen (Master Batch Records) Erstellen und Überarbeiten sowie Überprüfen von Rezepten/Methoden Ihr Zuständigkeitsbereich umfasst des Weiteren Tätigkeiten im Bereich Operational Readiness (u.a. Materialmanagement; Probenhandling; Environmental, Health and Sa

Associate Director, Biostatistics (Late Stage) Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary Position leads complex studies in study design, statistical analysis and interpretation of results with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to Health Authorities globally with some supervision. This position also guides contract research organization (CRO) programmers and statisticians in preparing analysis files and performing statistical analyses. Additionally, this position interacts with study teams, as well as statisticians and programmers at CROs. This position works under some supervision to solve complex study problems. Responsibilities Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol developm

Mitarbeiter (Pharmakant/PTA/CTA/MTA) (m/w/d) für die Arzneimittelherstellung befristet auf 2 Jahre Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Angaben zur Tätigkeit: Als Mitarbeiter (m/w/d) (Pharmakant/PTA/CTA/MTA) für die Arzneimittelherstellung sorgen Sie eigenständig für die Bedienung, Rüstung und Reinigung unserer Maschinen zur Herstellung von Tabletten, Filmtabletten, etc. nach Vorgabe von Herstellvorschriften Wir vertrauen Ihnen die Durchführung von Wartungs-, Kalibrierungs- und Reinigungstätigkeiten im Herstellbereich an, die Sie nach Vorgabe von Standardarbeitsanweisungen an Produktions- und Betriebsanlagen durchführen Laufende Kontrollen der Prozess- und Qualitätsparameter sowie die Durchführung und Dokumentation von In-Prozess-Kontrollen gehören ebenso zu Ihrem Aufgabenpacket Ihr Tätigkeit umfasst auch die Beachtung von Hygiene-, Sicherheits-, Betriebs- und Umweltvorschriften sowie das Arbeiten und Dokumentieren nach Vorgabe von GMP „Gute Herstellungspraxis für Arzneimittel und Wirkstoffe“ Wir freuen uns ebenso über Ihre Mitwirkung bei der verfahrenstech

Team Lead GMP/GDP QA Affiliate Management - 70001684 Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. The Position: The Team Lead GMP/GDP QA Affiliate Management will be responsible for managing a team ("country cluster") of local Quality Managers/Responsible Persons and Quality Experts located in DSE/DSE EU Affiliates. Roles and Responsibilities: Lead a multinational team of approx. 5-7 Senior Quality Managers, Quality Experts, and externals in EU Affiliates Plan, coordinate, and manage operational QA support through Quality Experts; prioritize resources according to local needs Supervise and enforce implementation of regional/global QA processes and systems in the DSE EU Affiliate country cluster Assure standardized execution of Quality processes in the country cluster Serve as the first point of contact for all quality-related topics and issues addressed by local Quality Managers/Responsible Persons and facilitate problem-solving and decision-making Provide profound expert knowledge to local Quality Managers and give gui

Oncology Clinical Educator - AR/MS/AL Work Model Remote Field (Daiichi Sankyo US) | Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary The Oncology Clinical Educator role provides disease state, REMS, and product safety education and training to key healthcare providers within Oncology clinics, and health care providers (HCPs) in both the hospital and clinic/office setting. The individual will work within a specified region to enhance disease, REMS, and product safety knowledge, coordinate and provide staff training, and enhance proper administration. The Oncology Clinical Educator (OCE) role is a position that is field based and is comprised of nurses working under the general direction of the Regional Director of Clinical Nurse Managers. The OCE is responsible for educating HCPs/clinics with infusion and related education for prescribed DSI products. The OCE serves as the disease state and product safety expert for their assigned territories. The OCE serves as a resource to clinical leaders by identifying disease state, REMS, and product safe

Associate Director GOMA Oncology Scientific Engagement Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary The Associate Director, GMA Oncology, Scientific Engagement is responsible for the execution of activities in support of Global Medical Affairs Scientific Engagement strategies and plan for the Solid Tumor or Hematology therapeutic area (TA), under the guidance of the Director, GMA Oncology Scientific Engagement Responsibilities Execution of Global Key External Experts (KEE) engagement strategy and operational plan. Management and updating of KEE mapping and engagement plans, and related systems used for global coordination of medical activities. Support coordination of Global scientific engagements (KEE, patient advocacy, professional society, and other HCP stakeholders) at major congresses, in collaboration with GMAT leads, regional and country medical leads, and other relevant internal cross-functional stakeholders. This includes alignment with Global Marketing, R&D, and Cancer Enterprise stakeholders. Suppor

Clinical Study Manager, Clinical Operations Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary The Clinical Study Manager is responsible for the delivery and execution of global clinical studies under the direction of a Study Delivery Lead. This role is primarily focused on tactical study delivery and reports to a Director or higher-level position. The position requires excellent written and verbal communication, project management skills, and attention to detail. The Clinical Study Manager will have routine interaction with key internal and external stakeholders to communicate project status, resolve issues, and troubleshoot routine inquiries. This position may require the Clinical Study Manager to take on a dual role of both operational strategy and study execution. Job Description Responsibilities Clinical Operations Study Management(Global) has primary accountability for operational execution and delivery of assigned clinical trials, including study level time, cost and quality deliverables. In a CRO

Senior Director, Clinical Safety Scientist Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary The Senior Director, Clinical Safety Science is a key leadership role responsible for shaping and advancing global safety strategy across the product lifecycle-from early development through post-marketing. This position oversees a team of Safety Scientists who partner with Safety Physicians and cross-functional stakeholders to ensure proactive safety surveillance, benefit-risk assessment, and risk mitigation planning for a group of assets. The Senior Director plays a pivotal role in influencing safety governance, driving innovation in safety science, and ensuring regulatory and compliance excellence. In addition to operational oversight, this role contributes to the development of global safety processes, talent capability building, and strategic alignment across the broader Clinical Safety and Pharmacovigilance (CSPV) function and the enterprise. Job Description Responsibilities Strategic Safety Leadership: Pr

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ウンドマネジメント事業部_営業職（神奈川県） JPN - Tokyo posted: Posted 25 Days Ago

Laboratory Technician / Laborant Lab Biologics LC/CE/GC (m/w/d) Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society. Die Position: Der / die Stelleninhaber/in ist verantwortlich für die ordnungsgemäße Durchführung analytischer Prüfungen und deren GMP-konforme Dokumentation. Angaben zur Tätigkeit: Durchführung von Freigabe- und Stabilitätsanalytik an biopharmazeutischen Arzneimitteln mittels modernster instrumenteller Analytik (HPLC, CE, zukünftig GC) in der kommerziellen Qualitätskontrolle. Analyse und Interpretation analytischer Daten unter Einsatz spezialisierter Software (z. B. Empower®) zur Sicherstellung präziser Ergebnisse. Lückenlose und sorgfältige Dokumentation aller Tätigkeiten in einem streng regulierten, qualitätsorientierten Laborumfeld (GMP). Durchführung von Wartungs- und Qualifizierungsarbeiten an hochmodernen Analysegeräten. Aktive Mitarbeit bei der Erstellung, Pflege und Optimierung von Prüfanweisungen sowie Laborprozessen. Etablierung, Validierung und Optimierung analytischer Methoden nach regulatorischen Vorgaben bei d

Senior Sales Engineer, Japan 13103, JPN, 1060032 | Tokyo, Japan