72 atomic-physics positions at Pfizer in us

Quality and Compliance Lead - Drug Product Supply Global Materials Management

Compliance Lead with a focus on GMP principals across our Global Materials Management group. The successful candidate will ensure the highest level of quality and compliance across all aspects of GMM

Study Operations Manager II

Start Up Project Manager, Site Intelligence Lead, Country Trial Manager, Site Excellence Partners, Site Relationship Partners, Site Care Partners, Contracts Lead, Regulatory Affairs, pCRO and others as

Clinical Study Team Lead - Obesity (Director)

and be accountable for effective study team operations Accountable for issue escalation and resolution Lead study team chartering and team health check process Governance & Decision Points Drive

Senior Associate Scientist, Process Safety

colleagues, complete review and witnessing of all experiments. Summarize and document results in process safety test reports Lead technology development and workflow initiatives to implement new capabilities

Process Safety Laboratory, Principal Scientist

-class process safety capabilities. Responsible for maintaining lab facilities in a neat and orderly manner complying with all local safety practices. In conjunction with the Groton, CT process safety lead

Scientist - Analytical GLP

cutting edge design and process development capabilities to accelerate and bring the best-in-class medicines to patients around the world. What You Will Achieve This is a laboratory-based position within

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, Clinician (Non-MD), Early Clinical Development

sub team(s) to ensure collaboration and seamless connectivity. ROLE RESPONSIBILITIES Responsibility to assist/lead development and execution of simple to moderately complex clinical studies; on more

Clinical Study Team Lead (Director)

. • Responsible for proactive risk management and inspection readiness for their clinical study(ies). Your responsibilities may also include: • Ensures comprehensive operational input to submission plan. • Lead the

Senior Associate Scientist - Purification

cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve The Senior Associate Scientist is responsible