The Manager, Regulatory Affairs Labeling will support global labeling projects by developing and reviewing labeling content for FDA submissions, tracking affiliate labeling, and ensuring consistency with regulatory standards. Responsibilities also include managing timelines for labeling changes and collaborating with global affiliates on proposed labeling revisions.

Lead and manage quality assurance for Contract Manufacturing Organizations (CMOs) ensuring compliance with FDA regulations and GMP guidelines. Oversee quality management systems, drug product management, process validation, and complaint investigations, while interacting with global teams to support continuous improvement and compliance.

The Manager, External Supplier QA-GMP is responsible for managing quality assurance of contract manufacturing organizations, ensuring compliance with FDA and GMP guidelines, supporting drug product management, participating in cross-functional teams, and overseeing validation and technical transfer activities to mitigate risks.

The Manager, QA Product Release Management is responsible for overseeing quality assurance activities related to the release of commercial and investigational medicinal products. This includes managing quality systems, conducting deviation investigations, handling complaints, and ensuring compliance with regulatory standards. The role involves cross-functional collaboration to support product quality and timely releases.

The Manager of Sales Training and Development focuses on developing training programs for oncology sales representatives. Responsibilities include creating training content, leading workshops, coaching, managing vendor relationships, and collaborating with stakeholders on training initiatives. The role emphasizes continuous learning and the effective delivery of product knowledge to sales teams, with a focus on compliance and the company culture.

This role supports the Global R&D organization by driving precise capacity planning and analysis. Responsibilities include developing advanced algorithms for resource management, establishing reporting metrics, and partnering cross-functionally to optimize resource deployment and productivity through data-driven strategies. Project management skills are essential for leading complex projects and establishing effective communication across teams.

The Executive Administrative Assistant provides advanced support to a functional executive, managing calendars, communications, and sensitive documents. Responsibilities include project management, stakeholder interaction, and upholding confidentiality while performing tasks with minimal supervision.

Provide strategic legal support as the primary legal advisor for the U.S. commercial operations in oncology, manage outside counsel, prepare legal documents, negotiate contracts, and lead cross-functional projects while fostering professional growth within the Legal Affairs Department.

The Exec Admin Assistant supports a functional executive by managing complex calendars, coordinating meetings and travel, creating documents, and acting on behalf of the executive in communications. They handle sensitive information and initiate projects, ensuring adherence to confidentiality and organizational needs.

The Senior Administrative Assistant will provide comprehensive support to the GMP Quality Assurance team, manage executive calendars, communicate between stakeholders, and handle office and project management tasks. Responsibilities include contract processing, payment management, and problem-solving in a fast-paced environment.

The Manager, RACMC oversees regulatory affairs for CMC projects, prepares submission documents, interacts with FDA, and manages development projects with supervision. They ensure understanding of regulatory guidance throughout the development process and support the technical team.

The Non-Regulated Implementation Services Lead oversees the planning and execution of non-regulated systems development, ensuring quality and efficiency aligned with business objectives. Responsibilities include integration testing, managing API-based integrations, collaborating with cross-functional teams, providing technical leadership, and managing vendor relationships.

The Marketing Intern will support the commercial brand team by developing marketing strategies and content, assisting with LCM initiatives, and managing projects related to congress strategy and execution. This role involves collaboration with various internal and external partners to meet business needs.

The intern will assist in communication tasks for Global R&D, including writing, designing visual content, and developing communication strategies while supporting senior employees with various projects and research.

The CMC Management and Operations Intern will design data structures to connect manufacturing data across global sites, contributing to the company's innovation in pharmaceutical therapies.

The Associate Director, Business Relationship Manager will strategically partner with business stakeholders in corporate functions, ensuring alignment between technology solutions and business goals. Responsibilities include managing demand from stakeholders, advocating for their needs, enhancing demand management processes, providing coaching on best practices, and measuring the success of digital initiatives while facilitating collaboration across teams.

The Digital Transformation Lead will oversee the development and implementation of IT systems to support Daiichi Sankyo's business functions, ensuring alignment with business goals and IT strategy. Responsibilities include collaboration with stakeholders, project management, overseeing IT transformations, and evaluating new technologies.

The Director will oversee the configuration and development of SAP SuccessFactors modules such as Performance, Compensation, and Variable Pay. Responsibilities include managing operations, technical support, data governance, and collaborating with stakeholders, while ensuring robust functionality and compliance with business needs.

The Manager, Project Lead - Program Management is responsible for ensuring timely delivery of clinical supplies, supporting project management leads, developing study supply plans, managing vendor relationships, overseeing clinical label development, and ensuring compliance with quality assurance processes.

The Director of Global Operational Excellence will develop and implement a continuous improvement strategy, optimizing processes using Lean and Six Sigma methodologies. Responsibilities include fostering a culture of improvement, leading a team of professionals, and leveraging data analytics to enhance operational performance while ensuring compliance with regulatory standards.