IT Solution Manager - GMP Production Systems

Novo Nordisk; Denmark; On-site; DKK 500,000 - 734,000; Full time

Job summary

Novo Nordisk in Denmark is seeking an IT Solution Manager for IT Operations 1 in CMC DP Pilots TS&IT at Måløv. You will help drive IT solutions enabling drug product development, collaborating with scientists, technicians, vendors and IT stakeholders to design, implement and maintain compliant systems.

You will contribute to operation, validation, documentation, cybersecurity, risk assessments and continuous improvement to keep production IT solutions reliable and in good standing with GMP

Qualifications

• Relevant technical education or equivalent experience.
• Several years in IT support, IT system management, or related roles.
• Experience with IT infrastructure, servers, networks, and databases.
• Experience with testing, validation, and technical documentation.
• Experience with manufacturing IT solutions, MES or process control is an advantage.
• GMP, data integrity, change control and risk assessments knowledge.

Responsibilities

• Maintain and operate IT Solutions and automation platforms.
• Support quality management system activities and data integrity.
• Support implementation, qualification and validation activities per GMP.
• Prepare and maintain technical documents and design specs.
• Drive cybersecurity, standardization and regulatory compliance.
• Lifecycle management: patching, backups, monitoring, risk assessments.
• Troubleshoot and drive continuous improvements for stable operations.

Skills

System administration

Troubleshooting IT issues

Server management

Documentation & QA

Data integrity & GMP

Communication skills (EN/DA)

Education

Technical education or equivalent experience

Tools

MES systems

Process control systems

Regulatory compliance tools

Job description

Novo Nordisk in Denmark is seeking an IT Solution Manager for IT Operations 1 in CMC DP Pilots TS&IT at Måløv. You will help drive IT solutions enabling drug product development, collaborating with scientists, technicians, vendors and IT stakeholders to design, implement and maintain compliant systems.

You will contribute to operation, validation, documentation, cybersecurity, risk assessments and continuous improvement to keep production IT solutions reliable and in good standing with GMP