Equipment Owner – Black Utility Systems

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

Benefits offered by this job

Incentives

Benefits

Total rewards

Job summary

Novo Nordisk in Kalundborg seeks an Equipment Responsible to own Black utility systems and ensure compliant, qualified operations across the plant. You will bridge multiple disciplines, from project handover to steady-state operation, focusing on reliability and lifecycle integrity.

The role emphasizes cross-functional collaboration, documentation discipline, and proactive problem-solving within a highly regulated pharmaceutical setting.

Qualifications

• Experience in GMP-regulated environments with strong compliance, documentation and quality mindset.
• Experience with qualification, validation, commissioning, or project execution is an advantage.
• Demonstrated ability to manage stakeholders across functions and cultures.
• Structured problem-solving and lifecycle ownership of utility systems.
• Experience in regulated manufacturing environments and complex facilities.

Responsibilities

• Take technical ownership of Black utility systems and ensure compliance, qualification and lifecycle integrity.
• Support commissioning, qualification, verification, equipment handover and startup activities.
• Maintain technical documentation, specifications and lifecycle plans; ensure inspection/audit readiness.
• Drive technical troubleshooting and SPS activities to improve reliability and performance.
• Support GMP-related activities including deviations, change management, investigations and audits.

Skills

Ownership mindset

GMP experience

Stakeholder management

Effective communication

Regulatory compliance

Education

Marine Engineer

Mechanical Engineer

Process Engineer

Automation Engineer

Job description

Novo Nordisk in Kalundborg seeks an Equipment Responsible to own Black utility systems and ensure compliant, qualified operations across the plant. You will bridge multiple disciplines, from project handover to steady-state operation, focusing on reliability and lifecycle integrity.

The role emphasizes cross-functional collaboration, documentation discipline, and proactive problem-solving within a highly regulated pharmaceutical setting.