57 Physics positions at Pfizer in california

Trial Master File Operations, Senior Manager

development and execution of control plans Utilize operational performance data to characterize state of control, improvement opportunities and drive process and system optimization Deliver effective business

Sr Director, Oncology Quality Risk Management Team Lead

development of new risks and evolving existing risks in relevant Quality Risk Management (QRM) tools. Provide feedback to QRM Business Process Owner (BPO) to continuously improve Integrated Quality Management

Site Quality Operations Leader (Diagnostics)

financial resources within the Global Business Unit. Direct a team of colleagues who are responsible for process documentation, training and monitoring of key processes and controls within Business Unit

Associate Research Fellow

, systems pharmacology, pharmacometrics, engineering, mathematics, physics or similar disciplines where modeling and simulation is emphasized. 10+ years of pharmaceutical industry or related experience in

Principal Scientist

pharmaceutical sciences, systems pharmacology, pharmacometrics, engineering, mathematics, physics or similar disciplines where modeling and simulation is emphasized. 2+ years of pharmaceutical industry or related

Manager, Clinician (Non-MD), Early Clinical Development

Sciences group by way of process improvement. Develop expertise navigating Pfizer compliance systems, registries (e.g. GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related

Senior Scientist, Molecular Pharmaceutics, Drug Product Design

cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. POSITION SUMMARY As a Senior Scientist in the Molecular

Asset Quality Lead (Director)

assets or CD&O process area and drive learnings across their tumor type(s). Lead Level 1 quality review/assessment during Due Diligence and/or Integration activities. Oversee program and study-level

Manager, Medical Writing

development process. Collaborates with project teams, subject matter experts, and quality lines to e nsure clear, factual, effective, and appropriately concise presentation of analyses and associated

Director, Global Regulatory Strategy

colleagues. Ensures that all regulatory development process commitments are clearly communicated, monitored and met. Acts as the point of contact for all internal Pfizer communication regarding the status