Scientist- Bioprocessing Upstream

Location Sanford, North Carolina, United States Overview We at Pfizer Global Supply are dedicated to manufacturing and distributing a broad portfolio of pharmaceutical products. This role is part of our Manufacturing Sciences and Technology (MSAT) organization, which supports the reliable, efficient, and compliant manufacture of innovative therapies and vaccines. Responsibilities Develop and qualify upstream models at bench and pilot scale to support commercial biologics manufacturing and technology transfers. Design and execute studies, as lead or team member, to support process optimization and investigation efforts. Analyze scientific data and communicate outcomes to relevant teams and managers. Author technical reports and electronic notebook entries in compliance with company expectations. Actively participate in group discussions by communicating problems and proposing solutions. Manage and execute independent projects alongside team-based project studies. Work under limited supervision, receive instructions on complex problems, and develop scientific activities to support team goals. Minimum Qualifications Bachelor’s degree with at least 2 years of experience; or Master’s degree with 0+ years; or Associate’s degree with 6 years; or high school diploma with 8 years of relevant experience. Deep understanding of upstream bioprocessing or related sub-field (e.g., microbiology, biochemistry, fermenters). Strong oral and written communication skills. Robust analytical abilities and proficiency with basic statistical methods (T-test, ANOVA, regression analysis) and graphing. Proficiency in using personal computers (Word, Excel, PowerPoint, scientific software). Comfortable and interested in using AI tools such as ChatGPT or Microsoft Copilot to improve efficiency. Experience troubleshooting equipment and scientific problems. Preferred Qualifications Proficiency in intermediate or advanced statistical methods including DOE design, PCA analysis, and other multivariate techniques. Experience or knowledge related to digitizing a laboratory environment (networking, databasing, user interface development). Experience or knowledge of GMP practices, including change management. Experience supporting commercial investigations. Experience developing an AI agent or digital workflow (e.g., Power App, Power Automate, Power BI). Experience working with microbial pathogens. Experience with facility design and/or troubleshooting equipment issues. Familiarity with DMAIC principles and processes. Physical/Mental Requirements Lifting, sitting, standing, walking, crouching, bending. Ability to perform complex data analysis and mathematical calculations. Work Schedule Shift and schedule flexibility is required as process timing dictates work. No routine travel is expected. Benefits Annual base salary range: $82,700.00–$137,900.00. Eligible for Pfizer’s Global Performance Plan with a bonus target of 10.0% of base salary. Benefits include a 401(k) plan with Pfizer matching and additional retirement contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health, dental, prescription drug and vision coverage. Relocation assistance may be available based on business needs. Application Details Last Date to Apply: 25 June 2026. Eligibility Candidates must be authorized to work in the United States. U.S. work visa sponsorship is not available for this role. EEO & Employment Eligibility Pfizer is committed to equal opportunity for all employees and applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or expression, national origin, disability, or veteran status. Pfizer is an E-Verify employer and complies with all applicable laws governing nondiscrimination and work authorization. #J-18808-Ljbffr Pfizer, S.A. de C.V