Join our dynamic Quality Assurance team as a Senior QA Engineer specializing in Computer System Validation and Data Integrity! This is an exceptional opportunity to lead the validation of cutting-edge GMP computer systems in a fast-paced, innovative CDMO environment. You'll work alongside a collaborative team of quality professionals who are passionate about ensuring patient safety through robust system validation and data integrity practices. As part of our growing organization, you'll have the opportunity to shape validation strategies from the ground up and make a meaningful impact on global pharmaceutical manufacturing. As our Sr. QA Engineer, CSV/DI, you will provide expert oversight of computer system validation activities across all GMP systems including process automation, cloud-based platforms, and laboratory systems. You'll be responsible for developing and approving validation strategies, qualification protocols, and lifecycle documentation while ensuring compliance with FDA, EMA, and other global regulatory requirements. This role requires strong technical expertise, regulatory knowledge, and the ability to present confidently to client auditors and regulatory inspectors. You'll lead the implementation of risk-based validation approaches and ensure comprehensive documentation throughout the entire computer system lifecycle.