Principal Validation Engineer

Use Your Power for Purpose The Principal Validation Engineer under Andover Site Technical Services (STS) is the principal owner of the Pfizer (PGS) Andover site validation program and master plan. The incumbent is responsible for delivering overall site validation program effectiveness and compliance in partnership with validation program owners across Andover site functions and the Pfizer network What You Will Achieve In this role, you will: • Establish and maintain overall Andover site validation philosophy and master plan in partnership with local validation program owners, technical subject matter experts, and relevant Pfizer global/network/site quality system principals applicable to biologics drug substance/drug substance intermediate production, testing, storage, and transport • Operate PMO for Validation Program Lifecycle Projects • Establish and maintain site governances necessary to interpret validation philosophies and polices, implement and improve uniform validation practices and approaches, as well as to measure and maintain site validation program health • Maintain STS departmental infrastructure, and provide planning support for third party services utilized in validation and other technical services; oversee third party service provider service level and quality of service • Program owner and expert for select technical/validation disciplines • STS capital project portfolio and expense planning • Lead site validation planning and management of validation activities for large capital or complex asset lifecycle projects Here Is What You Need (Minimum Requirements) • BA/BS degree in Science or Engineering with 6+ years of experience or MBA/MS with 5+ years of experience or PhD/JD with 1+ year of experience or MD/DVM with any years of relevant experience • Experience in pharmaceutical, biopharmaceutical or biotechnology industry • Experience or broad knowledge in biopharmaceutical development, manufacturing, and lifecycle management • Experience in project management and leading complex projects • Effective written and verbal communication skills • Strong interpersonal skills and the ability to work collaboratively in a team environment across various business functions Bonus Points If You Have (Preferred Requirements) • Experience developing philosophies/approaches for or managing validation programs applicable to the manufacture of biopharmaceutical drug substance, drug product, or medical device • Active participation in industrial/professional organization focused on advancing biopharmaceutical development, manufacturing, regulatory practices • Demonstrated ability to lead or build teams for complex technical projects involving risk management • Demonstrated leadership in a matrix organization     Physical / Mental requirements • Ability to perform mathematical calculations, scientific computation, complex data analysis, verbal communication, written communication Non-Standard work schedule, travel or environment requirements • Occasional domestic and international travels • Occasional off-hour support to address time-sensitive production and business-related issues Other job details • Last day to apply: July 17th, 2026 • Work Location Assignment: Hybrid     The annual base salary for this position ranges from $124,400.00 to $207,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfi