The QA Specialist at Eisai will execute quality assurance processes, review documentation, conduct investigations, and provide guidance to teams. The role involves supporting process improvements, managing inquiries related to quality areas, and developing quality procedures to meet company guidelines.

The Associate Director is responsible for the operational aspects of the lecanemab global launch plan and project management, liaising between teams and stakeholders. Tasks include managing schedules, budgets, project progress, and preparing status reports while driving effective communication and continuous improvement within the Global Alzheimer’s Disease office.

The Director, Global Infrastructure Office Lead is responsible for overseeing infrastructure programs and projects, managing budgets, resources, and vendor relationships. This role includes monitoring progress, tracking issues, and ensuring compliance with standards. The director will also implement performance measures, optimize costs, and report regularly to senior leadership, while fostering team performance within a fast-paced environment.

The Associate Director of QA Biologics is responsible for overseeing product compliance, managing quality processes and audits, ensuring regulatory adherence, and leading a team. This role involves monitoring metrics, managing external partners, and contributing to continuous improvement in the quality assurance domain within the biopharmaceutical industry.

The Project Manager, Change Management will oversee post-market activities related to global biological pharmaceutical products. Responsibilities include strategic planning, regulatory compliance, risk evaluation, project management, and cross-functional collaboration to optimize product portfolios and ensure regulatory adherence.

The Senior QC Compliance Specialist, Biologics is responsible for overseeing routine release and stability testing of commercial biologics. Key duties include monitoring compliance and data integrity, technical review of laboratory data, authoring quality documentation, and collaborating with various teams to ensure testing accuracy and timely completion.

The Associate Director will lead pharmacometric strategies to advance clinical research in Neuroscience. Responsibilities include developing complex pharmacometric models, representing Pharmacometrics in decision-making, and integrating diverse data approaches. Strong leadership and collaboration across projects are essential.

The Associate Director leads Global R&D Discovery IT operations, ensuring excellent user experience and compliance in IT services. Responsibilities include overseeing a global services portfolio, managing budgets, service delivery lifecycle, and leading a team of technical staff for support and improvement initiatives.

The Principal Researcher/Associate Scientist will develop bioanalytical methods for analyzing small molecules, conduct in vitro ADME studies, manage workflow logistics, communicate research results, and maintain laboratory documentation. Responsibilities include analyzing pharmacokinetic data and monitoring studies at CRO partners, as well as collaborating with internal and external teams.

The Discovery IT Portfolio Lead is responsible for managing the IT project portfolio in Discovery R&D, ensuring projects are delivered on time and budget. This role involves strategic planning, stakeholder communication, and oversight of project governance, risks, and budgets, while collaborating with multidisciplinary teams and external vendors to achieve project goals.

The Process Associate I will handle operations of cell culture-based production equipment in a cGMP biopharmaceutical plant. Responsibilities include executing process development, documenting studies, troubleshooting equipment issues, and ensuring compliance with regulatory standards, while working cross-functionally with other departments.