IT Compliance Professional

Novo Nordisk

. Help ensure IT and automation systems supporting manufacturing are compliant, reliable and ready for future needs .

Posted 10/4/2026full-timeBagsværd • DenmarkMid-LevelSenior💰 DKK 651,000 - DKK 956,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in IT validation and compliance within GxP-regulated environments, with a strong focus on regulatory compliance requirements, quality assurance methods, and risk-based validation strategies. Capable of leading projects, mentoring teams, and effectively communicating across diverse stakeholders.

Highest-signal resume keywords

IT ValidationRegulatory ComplianceGxP ExperienceQuality Assurance MethodsProject Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Validation PlansTest StrategiesGAMP 5Computerised Systems ValidationInfrastructure ValidationAI ValidationMachine Learning Validation

Soft Skills

CommunicationOwnershipCollaborationMentoringStakeholder Management

Tools & Technologies

SOPsCompliance GuidanceTraining Requirements

Industry Keywords

CGMPGxPQuality ManagementRisk-Based ValidationCross-Site Compliance

About the role

Key responsibilities & impact

Help ensure IT and automation systems supporting manufacturing are compliant, reliable and ready for future needs
Shape risk-based validation strategies for GxP computerised systems, infrastructure, AI and machine learning technologies
Advise on validation plans, reports, test strategies and other deliverables
Support reviews when required
Represent the department during audits and inspections
Coordinate effective handling of compliance gaps and findings
Drive implementation of new quality and regulatory requirements
Provide ad hoc compliance guidance to projects and operations
Maintain and simplify local processes, including SOPs, guides, training requirements and supporting instructions
Lead local projects and process improvements
Ensure operational management is considered in IT projects
Work with local stakeholders, IT functions, quality, manufacturing sites and external suppliers
Contribute to cross-site compliance and validation networks and interact with global strategic partners
Coach and mentor others

Requirements

What you’ll need

Bachelor’s or master’s degree in computer science, engineering, life sciences or a related field
3–5 years of experience with IT validation and compliance in a GxP-regulated environment
Hands-on experience validating computerised systems and infrastructure
Strong knowledge of regulatory compliance requirements, quality assurance methods and GAMP 5
Ability to communicate with colleagues and management, take ownership, and plan and deliver work independently
Ability to create results across functions, cultures and virtual international teams
Ability to navigate differing stakeholder interests with sound business understanding
Fluency in English
Experience within cGMP is useful but not essential
Experience validating AI or machine learning technologies is useful but not essential

Benefits

Comp & perks

Continuous learning
Career development
Benefits tailored to your life and career stage
Short-term and/or long-term incentives may be included
Other employee benefits based on position level, location, functional area and relevant market benchmarks
Opportunity to work independently and make your voice heard
On-the-job growth through new technologies, cross-site networks and colleagues across functions
Coaching and mentoring opportunities