Promote and maintain global standards, policies, and procedures for Computer System Validation (CSV), IT Governance, and Data Integrity. * Establish and maintain risk-based validation frameworks in accordance with GAMP 5, FDA 21 CFR Part 11, EU Annex 11, Data Integrity guidance, and company standards. * Support health authority inspections, internal audits, supplier audits, and regulatory inquiries involving computerized systems and data integrity. * Provide expert guidance regarding GxP regulations, Data Integrity expectations, and quality risk management. * Bachelor's degree in a scientific, engineering, information technology, computer science, pharmacy, or related discipline required. * Minimum 12 years of experience within the pharmaceutical, biotechnology, medical device, or oth
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