Experienced in ensuring that computerized systems meet regulatory compliance and quality standards within the life sciences, pharmaceutical, and healthcare industries. Proficient in developing and executing validation protocols, conducting risk assessments, and preparing comprehensive documentation to support system validation. Skilled in collaborating with cross-functional teams to ensure system integrity and regulatory compliance, including 21 CFR Part 11 and GxP guidelines. Strong analytical and problem-solving abilities with a focus on maintaining high standards of quality and safety.