Associate MSAT Engineer

REGENERON PHARMACEUTICALS, INC.

GLOBAL   Job Title:           MSAT Engineer- Assoc, Int, Sr Prepared on:    24Jun2026   Summary: Provides manufacturing science and technology (MSAT) support for internal and/or external manufacturing operations across multiple modalities. Supports technology transfer, process validation, and ongoing manufacturing support activities to ensure processes are implemented, operated, and maintained in a compliant and reliable manner.   Essential Duties and Responsibilities: ·         Support internal and external technology transfer activities, including participation in facility fit assessments and high-level gap assessments. ·         Generate, review, and support documentation associated with technology transfer, including process descriptions, master plans, reports, and technical documents. ·         Provide technical support to manufacturing operations during start-up, engineering runs, validation, and routine manufacturing. ·         Leverage engineering principles during problem solving and process support. ·         Review manufacturing documentation generated by receiving sites, including batch records, automation recipes, SOPs, and change documentation. ·         Gather, trend, and analyze process data to support process understanding and ongoing process performance monitoring. ·         Participate in investigations and deviation assessments and support identification of root causes and corrective actions. ·         Apply engineering principles to the development and execution of manufacturing support activities. ·         Analyze data using a combination of statistics, engineering principles and other techniques to gain insight into manufacturing support activities. ·         Work effectively in cross-functional teams to support timely execution oSAT deliverables. ·         Ensure activities are performed in accordance with cGMP. ·         May lead others. ·         Perform other duties as assigned. ·         Travel to internal manufacturing sites or external partners as required (<10% to 50%).   Education and Experience: ·         Associate Engineer: Requires BS/BA in an engineering discipline or equivalent combination of education and experience. ·         Engineer: Requires BS/BA in an engineering discipline with 2&#43; years of relevant experience in a pharmaceutical/biologics cGMP manufacturing, MSAT, process development, or analytical environment; or MS with 0–1&#43; years; or equivalent combination of education and experience. ·         Sr Engineer: Requires BS/BA in an engineering discipline with 5&#43; years of relevant experience; or MS with 4&#43; years; or PhD with 0-2 of relevant experience, or equivalent combination of education and experience.     Knowledge, Skills, and Abilities: ·         Knowledge of biopharmaceutical manufacturing processes and technology transfer principles. ·         Ability to apply engineering principles to evaluate process and product behavior and to develop defensible conclusions. ·         Familiarity with cGMP requirements, data integrity principles, and regulated documentation practices. ·         Ability to analyze and interpret manufacturing and analytical data; communicate findings clearly in written and verbal formats. ·         Strong collaboration skills and ability to work effectively in cross-functional and cross-site environments. ·         Ability to manage multiple priorities and deliver high-quality outputs within timelines.     Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for