IT Compliance Partner

Cari; Taastrup; On-site; DKK 743,000 - 1,092,000; Full time

Job summary

Novo Nordisk is seeking an IT Compliance Partner for Global Manufacturing & Supply IT - Supply Chain in Taastrup, Denmark. You will act as the key compliance expert and trusted advisor, strengthening governance, risk management and compliance across a global environment to keep critical IT systems inspection-ready.

You will work with stakeholders across production, logistics, device manufacturing and global supply chain processes, ensuring regulatory expectations are met while balancing business

Qualifications

• Strong knowledge of GxP, cGMP, GAMP, 21 CFR Part 11, ISO and COBIT standards.
• Experience in advisory or consulting roles influencing stakeholders without direct authority.
• Excellent communication skills with technical and senior leaders.

Responsibilities

• Act as the primary IT compliance partner for Supply Chain IT.
• Drive compliance improvement initiatives and risk reporting.
• Support audits and inspections; coordinate remediation plans.

Skills

IT compliance

GxP & 21 CFR Part 11

Regulated IT environments

Stakeholder management

Communication

Education

MSc or BSc in CS/Engineering/Business Administration

Job description

IT Compliance Partner

Job Title: IT Compliance Partner

Department: Global Manufacturing & Supply IT - Supply Chain

Location: Taastrup, Denmark

Your impact begins here

As IT Compliance Partner, you will act as the key compliance expert and trusted advisor for Supply Chain IT. You will strengthen governance, risk management and compliance practices across a complex and global environment, making sure the critical IT systems supporting Novo Nordisk's pharmaceutical production remain inspection-ready. Your work helps keep the systems behind production, logistics, device manufacturing and global supply chain processes compliant, so our products can keep reaching the people who need them.

What you’ll bring

To succeed in this position, we imagine that you bring a strong combination of technical expertise, compliance knowledge and stakeholder management capabilities, including:

• An MSc or BSc degree in Computer Science, Engineering, Business Administration or a related field.
• Several years of experience working with IT compliance, validation, quality, governance or regulated IT environments within the pharmaceutical industry.
• Strong knowledge of GxP, cGMP, GAMP, 21 CFR Part 11, ISO and COBIT standards, and validation requirements for business-critical IT systems.
• Experience in advisory or consulting roles where influencing stakeholders and driving change without direct authority has been essential.
• Excellent communication skills and the ability to engage confidently with both technical specialists and senior leaders.

As a person, you are analytical, quality-minded and structured. You are comfortable challenging the status quo, driving new ways of thinking and balancing compliance requirements with business needs. You bring energy, curiosity and the confidence to lead discussions, facilitate alignment and create momentum across diverse stakeholder groups.

What you’ll do

This role combines strategic thinking, tactical planning and operational execution, making it ideal for someone who enjoys working across organisational levels while influencing without direct authority. You will:

• Act as the primary IT compliance partner across Supply Chain IT, providing guidance on governance, risk management, validation and regulatory requirements.
• Drive compliance improvement initiatives, risk reporting activities and standardised ways of working in collaboration with stakeholders and relevant networks across the organisation.
• Support audits and inspections, coordinate remediation plans and ensure findings are effectively addressed.
• Advise projects on IT governance and compliance requirements.
• Build and lead a strong compliance network within Supply Chain, influencing stakeholders and ensuring continuous alignment with evolving regulatory expectations.

Success in this role means quickly establishing credibility, building relationships across a broad stakeholder landscape, assessing the current compliance landscape and proactively driving improvements that enable business success while maintaining high-quality standards.

Who you’ll work with

You will join Global Manufacturing & Supply (GMS) IT within the Supply Chain organization, a global area responsible for the IT and automation systems that support Novo Nordisk's manufacturing and supply chain operations. The department oversees critical systems that enable production, logistics, device manufacturing and global supply chain processes.

The team is relatively small and highly specialised, made up of experts responsible for key domains across architecture, governance and compliance. While you will be the primary compliance lead within the team, you will collaborate closely with a wider network of compliance professionals, risk coordinators, validation experts, architects, project managers and business stakeholders across Novo Nordisk and the wider Global Manufacturing & Supply network.

Your manager will be Luise Dam, Sr. Director. (Confirm reporting line.)

What you can expect here

You will work in an international, collaborative environment built on knowledge sharing, where specialists have significant ownership and influence on strategic decisions. You will be trusted to make your voice heard, bring your expertise to the table and help set the direction for how compliance is done across Supply Chain IT.

At Novo Nordisk, you’ll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development and benefits tailored to your life and career stage.

Salary

For this role, the Annual Base Salary ranges from DKK 742,600 to DKK 1,091,600, corresponding to the level of the position. The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge and relevant experience.

Incentives and Benefits

The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.

Learn more about our Reward Philosophy here.

For further information about the position, Luise Dam, Sr. Director, at lukrnovonordisk.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes - we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.