The Cloud and Infrastructure Intern will focus on AWS Cloud Optimization, reviewing and recommending enhancements for cloud infrastructure services while ensuring security. Responsibilities include analyzing resource utilization, transferring manual deployments to Terraform code, and collaborating with teams to migrate legacy applications to the cloud. The role offers exposure to Infrastructure as Code practices and cloud management.

The Sr. Neurology Account Specialist will generate demand by conveying complex clinical information to healthcare professionals (HCPs) and stakeholders. Responsibilities include executing strategic key-account plans, managing business opportunities, engaging with local healthcare systems, and collaborating with multidisciplinary teams while adhering to compliance standards.

The Senior Manager, GxP Systems Quality Assurance at Eisai is responsible for ensuring compliance with global regulations, providing guidance on process improvements, conducting audits, and facilitating training within the IT organization. The role involves collaboration with stakeholders for policy maintenance and monitoring regulations to support quality principles across the organization.

The Manager, LIMS is responsible for managing and supporting the Laboratory Information Management System (LIMS) within the Quality Assurance unit. This includes configuring, maintaining master data, developing reports, training users, and ensuring compliance with regulatory standards. The role involves cross-functional collaboration and support for related quality systems like TrackWise and Veeva, with an emphasis on project management and system upgrades.

The Head of Site Operations will oversee facility administration at Eisai's genetics-guided dementia discovery site, managing operations, budget, maintenance, safety compliance, and fostering site culture while leading community outreach and large projects.

The role involves providing scientific leadership in pharmacometric strategies, modeling neurodegenerative diseases, and integrating various modeling and statistical techniques to support drug development in neuroscience.

The Senior QC Compliance Specialist, Biologics oversees routine release and stability testing of commercial biologics at contract laboratories, ensuring data integrity and regulatory compliance. Responsibilities include monitoring testing, reviewing data, authoring reports, supporting analytical method validation, and collaborating with various teams for quality control.

The Project Manager, Change Management oversees post-market activities for global pharmaceutical products, focusing on change control, strategic planning, regulatory compliance, and project management. This role involves collaboration with cross-functional teams to ensure regulatory assessments are completed, and risk evaluation and mitigation strategies are developed for product lifecycle management.

The Associate Director, QA Biologics will oversee quality assurance for biopharmaceutical products, ensuring compliance with regulations and company standards. Responsibilities include managing product oversight, audit readiness, and continuous improvement, as well as leading a team and driving process management. The role involves significant interaction with regulatory inspections and external partners.

The Associate Director, Global Discovery Solution Architect is responsible for designing data and delivery architectures and systems for research environments. They will lead a technical team, manage the technology roadmap, and collaborate with stakeholders to align solutions with business needs, ensuring best practices in security and innovation.

The Process Associate I will operate and maintain media/buffer/washer/autoclave equipment in a cGMP biopharmaceutical plant. Responsibilities include executing process development, technology transfer studies, data interpretation, and documentation. The role requires ensuring compliance with regulations and providing cross-functional support in a team-oriented environment.

As a QA Specialist at Eisai, you will be responsible for executing and managing internal and external quality processes, conducting investigations for root cause analysis, reviewing documentation, providing training to cross-functional teams, and developing quality procedures to ensure compliance with regulations while supporting data analysis for quality metrics.

The Discovery IT Portfolio Lead at Eisai is responsible for delivering strategic IT projects within the R&D Discovery domain. This role includes project management, governance, and collaboration with various teams to ensure projects align with business objectives and are completed on time and within budget. Additionally, the lead will coach teams on project management best practices and drive adoption of project methodologies.

The Principal Researcher/Associate Scientist will develop bioanalytical methods, conduct in vitro ADME studies, and analyze pharmacokinetic data to support discovery projects in drug development. Responsibilities include maintaining laboratory records, communicating results, and ensuring compliance with standard operating procedures.

The Director of the Western Supply Chain Management Unit at Eisai is responsible for ensuring a continuous supply of quality pharmaceutical products, managing relationships with third-party manufacturers, leading cross-functional teams, and overseeing import/export compliance. This role is integral to the launch of new products and supply planning across various regions while maintaining a focus on patient needs.

The Senior Tax Manager ensures compliance with state tax laws, oversees state income tax accounting, prepares complex tax returns, assists in financial forecasts, manages tax audits, conducts tax research, and maintains internal control environments.

The Associate Director of Global Alzheimer's Project Management is responsible for managing the operational aspects of the lecanemab global launch plan, overseeing project schedules and budgets, facilitating communication among teams, and ensuring alignment and accountability across functions in the Global Alzheimer's Disease office.

The Scientist I position focuses on developing bioanalytical methods using LC-MS/MS, conducting in vitro ADME studies, and collaborating with teams. Responsibilities include method development, data analysis, documentation, technical supervision, and contributing to regulatory filings and external collaborations.