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As a Manager of End Point Engineering at Pfizer, you will develop enterprise level solutions for managed print and Windows PCs, manage devices with Intune and other tools, and ensure compliance and security of endpoint devices. You will collaborate with engineers and cross-functional teams, maintain budgets, manage escalated issues, and lead projects to drive continuous improvement in endpoint engineering.

The Director, Vaccine Immunologist will oversee the development of vaccine-induced immune response assays, manage multiple immunoassay development projects, and serve as a subject matter expert. Responsibilities include collaboration within vaccine research, leading a team of scientists, and ensuring compliance with relevant guidelines while presenting findings to senior leadership.

The Associate Director, Clinician, Medical Monitor for Vaccines provides medical oversight for clinical trials by ensuring patient safety, conducting safety reviews, contributing to protocol development, and collaborating with study teams for data quality and integrity. Additional responsibilities include training study teams and remains accountable for compliance with regulatory requirements.

The Director of AIDA R&D AI & Data Solutions Engineering will lead and manage a data solutions engineering team, focusing on the maturity and delivery of innovative data solutions. Responsibilities include project management, designing scalable solutions, ensuring compliance, and collaborating with business stakeholders to define project goals and deliverables.

The Director, AIDA R&D Program Planning and Execution at Pfizer will lead portfolio management and finance practices while optimizing resources across the R&D AIDA portfolio. This role involves serving as a liaison for portfolio transparency, defining operational metrics, and managing organizational oversight in a collaborative and strategic manner.

The Associate Director, Clinician, Medical Monitor is responsible for providing medical and scientific expertise for clinical trials, ensuring safety throughout the study, contributing to protocol design, and supporting the study team. Key responsibilities include safety monitoring, protocol development input, and communication with study sites regarding safety information.

The Associate Manager II provides design control support for biopharmaceutical projects, ensuring compliance with regulatory standards. Responsibilities include authoring design control documents, managing risks, and collaborating with cross-functional teams across global sites. The role integrates knowledge of biologics and device development within the product lifecycle, while supporting audits and investigations.