Senior IT Compliance Analyst - IT & OT - GMP

Role: IT Compliance Subject Matter Expert supporting pharmaceutical manufacturing at Novo Nordisk's Virginia site, focusing on validation, process improvement, and regulatory compliance for IT systems in Chemical API development. Responsibilities: develop validation documentation, conduct risk assessments, guide project teams on validation and qualification, ensure regulatory adherence, facilitate project transitions to service operations, participate in audits and inspections, and mentor team members. Requirements: Bachelor's Degree in IT/Science/Engineering with 7+ years in IT compliance and 5+ years in validation, preferably within pharma; excellent communication, problem-solving, and collaboration skills; proficiency in Microsoft Office. Preferred: Master’s degree, CISA or Lean Six Sigma certification, experience supporting audits, GxP environments, change management, and IT incident/problem/change processes. HighValue: pharma manufacturing, GxP compliance, validation & testing of IT solutions, regulatory audits, Chemical API development, up to 10% travel, onsite role in Virginia.