Senior Associate Scientist

Requirements

• 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
• 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
• 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
• Relocation assistance may be available based on business needs and/or eligibility.
• Candidates must be authorized to be employed in the U.S. by any employer.
• U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
• Sunshine Act
• Pfizer reports payments and other transfers of value to heal

Benefits

Additional Information

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.

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