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The role involves overseeing clinical data review to ensure data integrity and quality in late-stage oncology trials, supporting clinical operations and collaboration with medical teams. The position requires analyzing safety and efficacy data, understanding regulations, and improving clinical procedures for successful trial execution.

The Antibody Drug Conjugate (ADC) Molecule Analytical Product Specialist will manage the transfer and validation of assays for antibody products, ensure compliance with ICH guidelines, and oversee analytical characterization for ADCs throughout development stages. The role involves collaboration with internal and external teams and supporting quality tasks necessary for drug efficacy and safety.

As a QC Planner, you will analyze chemical, biological, and microbiological products, ensuring compliance with quality standards. You will perform testing, maintain cGMP laboratories, develop training plans, and support audits, contributing to efficient operations in the pharmaceutical industry.

As a QC Scientist, you will support Pfizer's quality programs by analyzing chemical, biological, or microbiological products. Responsibilities include environmental testing, analytical testing, training junior colleagues, and participating in regulatory documentation. You will ensure compliance with quality standards and Good Manufacturing Practices while influencing team projects with your scientific expertise.

The Director of Clinical Research will coordinate and lead the development of first-in-man and proof-of-concept studies for novel therapies in Immunology and Inflammation. Responsibilities include designing clinical trials, collaborating with various teams for implementation, ensuring safety across studies, preparing critical documents, and fostering collaboration within the clinical research environment.

The Lead Platform Engineer at Pfizer will lead teams to deliver and implement scalable platform solutions. Responsibilities include platform design, infrastructure management, and guiding engineering efforts to meet program objectives. Collaboration with cross-functional teams is critical, along with providing consulting and risk identification.

As a Sterile Manufacturing Operator, you will support engineering teams by preparing documentation, conducting analyses, and performing manual packaging operations. Responsibilities include inspecting products, maintaining a clean work environment, and assisting in training. You will prioritize workflows effectively and collaborate with maintenance on equipment issues while adhering to SOPs and safety regulations.