Senior Associate Scientist
PfizerAbout the role
Use Your Power for Purpose
At Pfizer, our purpose is to deliver breakthroughs that change patients’ lives. As a Senior Associate Scientist, you will be at the forefront of this mission, working within our Research & Development division. Your role will be pivotal in translating advanced science and technologies into therapies and vaccines that matter most. By leveraging cutting-edge design and process development capabilities, you will help accelerate the delivery of best-in-class medicines to patients globally, ultimately improving their lives.
What You Will Achieve
In this role, you will:
Conduct qualitative and quantitative analyses of various compounds and biologics to determine their properties during chemical syntheses, fermentation, or drug product development
Perform analytical method lifecycle activities such as development, validation, and transfer activities for both small molecules and complex formulations
Maintain written records of all experimental work in compliance with GLP/GMP and departmental SOPs
Assist in the maintenance and renewal of laboratory instruments, systems, or apparatus, and improve safe and effective working practices
Attend project team and brainstorming meetings to present data and apply technical skills to assignments
Work under moderate supervision with regular review and identify activities to support work group/project team goals
Contribute to the achievement of immediate work group goals and collaborate with other team members
Prioritize work to meet project deadlines and ensure participation and contribution as a team member
Continuously improve safe and effective working practices in the laboratory environment
Responsible for performing and troubleshooting analytical assays, while applying these methods across a board range of early and late-stage products in a cGMP environment.
Qualifications
Must Have
BA/BS with 3 to 5 years of experience performing biotherapeutics testing in a GMP environment.
Master's Degree with 4 to 6 years of experience performing biotherapeutics testing in a GMP environment.
Strong documentation skills and attention to detail
Experience with method validation
Ability to extract relevant information from scientific literature
Proficiency in recording observations, facts, data, and conclusions during experimental work or cGMP investigations
Solid understanding of fundamental analytical chemistry, including functional group recognition and compound characterization
Experience using spectroscopic and chromatographic techniques
Experience in GMP laboratory operations and logistics
Effective interaction with peers and leaders as part of a multi-disciplinary team
Strong verbal and written communication skills
Nice to Have
Understanding of various scientific software or software used in pharmaceutical or production environments
Good Laboratory Practices (part of GxP) and Good Manufacturing Practices (also cGMP) knowledge
Problem-solving skills and the ability to make decisions based on limited options
Initiative and proactive approach to tasks and projects
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
PHYSICAL/MENTAL REQUIREMENTS
Position requires occasional light lifting and periods of standing, sitting, or walking.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Position requires occasional off shift (evenings).
Work Location Assignment: On Premise
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