Key skills
AIRisk ManagementCommunicationProblem SolvingCollaboration
About this role
Use Your Power for Purpose
At Pfizer, our purpose is to deliver breakthroughs that change patients’ lives. Your work will leverage cutting-edge design and process development capabilities to accelerate and deliver best-in-class medicines to patients globally. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, your contributions will be vital in helping Pfizer achieve new milestones and make a global impact on patient health.
What You Will Achieve
Conduct qualitative and quantitative analyses of various compounds and biologics to determine their properties during chemical syntheses, fermentation, or drug product development
Utilize scientific judgment to adapt standard methods and techniques, drawing on prior experience and consulting with colleagues
Apply technical skills and knowledge proactively in projects, making decisions to resolve moderately complex problems, and receive instructions on complex problems with periodic review
Establish analytical procedures, interpret technical data, and develop scientific activities/projects to support team goals
Communicate progress, plans, requirements, and risks to senior analysts, managers, stakeholders in partner groups, and higher management through written reports and presentations
Actively participate and report progress in cross-functional project teams to meet customer expectations, project milestones, and Good Manufacturing Practices (cGMP) standards
Prepare and review technical documents, including validation protocols, analytical test procedures, investigation reports, and change controls, and support the development, qualification, validation, and transfer of cell-based and immunoassays for clinical development
Here Is What You Need (Minimum Requirements)
BA/BS with at least 6 years of experience or MBA/MS with at least 4 years of experience
Experience with interdisciplinary drug development teams
Industrial experience in developing analytical strategies and methods to support product and process development
Proficiency in assessing the quality and characteristics of biotherapeutics
Experience in a regulated environment such as Good Laboratory Practices (part of GxP)
Demonstrated technical expertise in functional verification of design
Working knowledge of applicable industry test standards, relevant regulatory guidance, Design Controls, and the Product Development Process
Bonus Points If You Have (Preferred Requirements)
Exceptional interpersonal skills and a proven track record of teamwork
Experience with advanced analytical techniques and instrumentation
Effective verbal and written communication skills
Ability to interact effectively with peers and leaders as part of a multi-disciplinary team
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
Laboratory Presence
Frequent work in analytical, microbiological, and bioassay laboratories is required. This includes handling
chemicals and cytotoxic/highly potent compounds (OEB-5 classification) with appropriate engineering
controls and PPE.
Mobility and Dexterity
Occasional light lifting and extended periods of sitting or standing are expected. The role may involve
bending, reaching, and working with lab instrumentation and data systems.
Cognitive Demands
High attention to detail, complex data analysis, and interpretation of analytical results are essential. The
role requires intellectual agility to troubleshoot methods and adapt to evolving regulatory and scientific
standards.
Communication and Collaboration
Strong interpersonal and communication skills are necessary to work effectively across cross-functional
teams and external partners.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Standard day shift, Monday through Friday. Occasional off-shift hours may be required to support urgent
Other Job Details:
Work Location Assignment: On Premise
Last day to apply: April 21
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 health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
Research and Development