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As a Scientist Process Development Engineer at Pfizer, you will focus on process characterization and optimization to support drug development, collaborating closely with engineering and operations teams to implement new manufacturing technologies and contribute to a culture of quality and safety in pharmaceutical production.

The Senior Associate, Drug Product Manufacturing Lead will coordinate and oversee multiple drug product manufacturing campaigns, ensuring compliance, and effective project management. Responsibilities include technical support, process improvement, and collaboration across several cross-functional teams while maintaining quality and safety standards.

Seeking a Principal Scientist with expertise in high content imaging and high throughput flow cytometry to support the small molecule portfolio at Pfizer's Primary Pharmacology Group. Responsibilities include designing disease-relevant assays, cell-based screening, validating therapeutic hypotheses, and utilizing image analysis methods. Ph.D. in Cell-Biology/Biochemistry and 5+ years of industry experience required. Must exhibit scientific excellence, leadership competence, and strong communication skills.

The Late-Stage Clinical Scientist is responsible for overseeing clinical trials in oncology, ensuring data integrity and compliance with regulations. This role involves collaboration with various teams, scientific writing, and analysis of clinical data. The candidate will also mentor others and help optimize clinical development procedures.

The Late-Stage Clinical Scientist is responsible for overseeing clinical trials within the Oncology portfolio, ensuring data integrity and quality while collaborating with clinical teams. Responsibilities include authoring clinical documents, reviewing safety and efficacy data, and leading efforts to enhance clinical procedures.

The Late-Stage Clinical Scientist is responsible for overseeing clinical trials within the Late-Stage Oncology portfolio, ensuring scientific oversight, data integrity, and quality. They work with clinical and operational teams to implement trial protocols, analyze safety data, and contribute to regulatory documents, while also mentoring team members and enhancing clinical procedures.

The Late-Stage Clinical Scientist is responsible for overseeing clinical trials in the Oncology portfolio, ensuring data integrity, quality, and scientific accuracy. This includes authoring important documents, analyzing safety data, collaborating with teams, and leading improvements in clinical development procedures.