Senior IT Compliance & Validation Analyst - IT & OT

Novo Nordisk; Petersburg (VA); On-site; USD 120,000 - 170,000; Full time

Benefits offered by this job

Health Insurance

Dental Insurance

Vision Insurance

401K matching

Paid time off

Tuition Assistance

Life & Disability Insurance

Employee Referral Awards

Job summary

Novo Nordisk seeks a seasoned IT Compliance Specialist in Petersburg, VA to lead validation and compliance across site projects. You will ensure solutions meet regulatory standards, coordinate with cross-functional teams, and drive continuous improvement in data integrity, patient safety, and product quality.

Strong English communication and pharma experience are preferred. This role requires collaboration with audit teams, continuous documentation updates, and adherence to Novo Nordisk

Qualifications

• Bachelor’s degree with 7+ years in IT compliance and 5+ years in validation/testing, preferably in pharma.
• Master’s degree with 5+ years in IT compliance and 3+ years in validation/testing; pharma experience preferred.
• Excellent written and verbal English communication.
• Strong customer service and collaboration skills.
• Excellent planning, organizing, decision making and ability to handle complexity.
• Strong computer skills and proficiency in MS Office.

Responsibilities

• Develop and maintain validation/Qualification documentation.
• Conduct risk assessments and mitigation analyses for compliance issues.
• Guide project teams on validation/qualification requirements.
• Monitor/document processes to ensure regulatory compliance.
• Facilitate handover of projects to service operations with stakeholders.
• Maintain system/process documentation per Novo Nordisk standards.

Skills

IT compliance

Validation & Testing

Communication in English

Project coordination

MS Office

Education

Bachelor’s Degree in IT/Engineering/Science

Master’s Degree in IT/Engineering/Science

Job description

Novo Nordisk seeks a seasoned IT Compliance Specialist in Petersburg, VA to lead validation and compliance across site projects. You will ensure solutions meet regulatory standards, coordinate with cross-functional teams, and drive continuous improvement in data integrity, patient safety, and product quality.

Strong English communication and pharma experience are preferred. This role requires collaboration with audit teams, continuous documentation updates, and adherence to Novo Nordisk