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About the Role

Pfizer's digital and 'data first' strategy aims to accelerate the development of impactful technology solutions for research, development, and medical functions. By fostering collaboration and information sharing through business technology, we strive to help employees discover the best healthcare solutions for our patients. As part of a team of innovators, you will play a crucial role in maintaining our systems and ensuring the security of our information. We seek dedicated colleagues like you to enhance the quality of patient care through fresh ideas and cutting-edge information technology solutions. Your expertise in informatics will be instrumental in advancing R&D by developing, supporting, and validating computer systems. You will generate high-quality assay data within a regulated cGLP (current Good Laboratory Practice) laboratory environment to bolster Pfizer’s research initiatives and streamline processes. Leveraging your technical and documentation prowess, you will ensure regulatory compliance for the Research Department’s software solutions. As an associate, your dedication to the job will drive the completion of project tasks and objectives. Your domain knowledge and commitment will foster a collaborative atmosphere among your colleagues. It is your diligence and focus that will empower Pfizer to reach new milestones and provide aid to patients worldwide.

Responsibilities

Translate business needs from laboratory and operations teams into practical info system solutions.
Partner with functional assay leads, operations leads, laboratory SMEs, and informatics partners to define requirements, support solution design, coordinate user testing, and manage project activities across the solution development lifecycle (SDLC).
Ensure info systems supporting regulated laboratory processes are fit for purpose, properly tested, and supported by appropriate documentation for validated environments.
Elicit, document, and maintain business and end-user requirements for new solutions and enhancements to existing solutions.
Support solution design discussions by ensuring proposed system functionality aligns with laboratory workflows, operational needs, compliance expectations, and end-user requirements.
Project manage assigned system initiatives through the solution development lifecycle, including requirements gathering, design review, testing, validation readiness, deployment support, and post-implementation follow-up.
Develop, review, and execute user acceptance testing activities to confirm system functionality meets approved business and end-user requirements.
Guide end users through testing activities, support test execution, document results, capture defects, and coordinate issue resolution with the technical teams.
Generate, review, and maintain documentation supporting validated systems, including requirements, test scripts, SOPs, change controls, and related project deliverables.
Facilitate regular project meetings with business stakeholders and technical partners to review priorities, status, risks, decisions, and action items.
Collaborate with quality, validation, laboratory, and technical teams to ensure system deliverables are aligned with regulated system expectations.
Maintain strict compliance with departmental, site, and corporate training, quality, and safety requirements.

Requirements

MS/MA in a science-related discipline such as computer science / mathematics or biological science with 1+ years of hands-on industry experience, OR BS/BA with 3+ years of hands-on industry experience.
Understanding of solution development lifecycle activities in a regulated or quality-driven environment.
Strong written and verbal communication skills.
Strong organizational skills with ability to manage multiple priorities, timelines, and stakeholders.
Proficient in Microsoft Office 365 applications.
Experience supporting validated systems in a pharmaceutical, biotech, laboratory, or regulated environment.
Familiarity with laboratory informatics systems such as LabWare LIMS and statistical analysis applications such as SAS.
Experience creating documentation such as requirements, test scripts, traceability matrices, SOPs, or user guides.
Experience working with cross-functional teams across business, quality, and technical organizations.
Working knowledge of SQL and basic understanding of computer programming language.
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.
Occasional evening and weekend work to meet critical deliverables.
Permanent work authorization in the United States.
Candidates must be authorized to be employed in the U.S. by any employer.

Skills

Informatics
Computer Science
Mathematics
Biological Science
Solution Development Lifecycle (SDLC)
Microsoft Office 365
LabWare LIMS
SAS
SQL
Computer Programming
AI tools
ChatGPT
Microsoft Copilot

Location

Hybrid

Work Type

Hybrid
Full-time

Experience Level

Senior Associate
1+ years of hands-on industry experience (with MS/MA)
3+ years of hands-on industry experience (with BS/BA)

Education Level

MS/MA in a science-related discipline
BS/BA

Salary/Compensations

$82,700.00 - $137,900.00
Bonus target of 10.0% of the base salary

Benefits

401(k) plan with Pfizer Matching Contributions
Additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage

About the Company

Pfizer's digital and 'data first' strategy aims to accelerate the development of impactful technology solutions for research, development, and medical functions.
Information & Business Tech

Equal Opportunity

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.