Sr MSAT Engineer

Senior MSAT Engineer Kelly® Science & Clinical is seeking a Senior MSAT Engineer for a 12-month contract position at a cutting-edge client in Houston, TX. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Pay: $60/hour Schedule: Mon-Fri Day Shift Onsite Overview Our client is an industry-leading company at the forefront of cell therapy manufacturing and CMC-GMP operations. This is a unique opportunity to join a cutting-edge organization where you will play a critical role in supporting quality records and PLI inspection readiness within a fast-paced, highly regulated biopharmaceutical environment. In this role, you will be responsible for owning and driving deviations, investigations, and CAPAs from initiation through closure, while partnering cross-functionally with Manufacturing, QA, and other technical teams. You will apply structured problem-solving methodologies, draft inspection-ready technical documentation, and support broader MSAT activities including process troubleshooting, change controls, and continuous improvement initiatives. Responsibilities: Own and drive deviations, investigations, and CAPAs from initiation through closure Support execution of PLI-enabling CAPAs and other inspection-readiness quality records Lead root cause analysis, technical impact assessments, and development of corrective actions Draft clear, technically sound, inspection-ready investigation and CAPA documentation Partner with Manufacturing, QA, and other technical functions to drive timely closure of quality records Apply structured problem-solving and risk-assessment methodologies Support broader MSAT activities as needed, including process troubleshooting, process assessments, change controls, manufacturing support, and continuous improvement Qualifications: Bachelor’s degree in engineering, Life Sciences, or a related technical field 7+ years of relevant biopharmaceutical manufacturing, MSAT, or Process Engineering experience Direct cell therapy manufacturing experience required Strong experience owning deviations, investigations, and CAPAs in a cGMP environment Excellent GMP technical writing and documentation skills Strong root cause analysis and cross-functional problem-solving capability Ability to work independently and manage multiple time-sensitive priorities Preferred: Autologous cell therapy experience Late-stage, pivotal, or commercial manufacturing/MSAT experience PLI / inspection-readiness experience Veeva or other electronic Quality Management System (eQMS) experience Houston-area based #J-18808-Ljbffr Kelly Services