Medical Device Development Engineer (12-month, Hybrid)

Novo Nordisk; Hillerød; On-site; DKK 570,000 - 838,000; Full time

Job summary

Novo Nordisk in Hillerød is seeking an Advanced Product Development Engineer to help develop and maintain medical devices that support people living with serious chronic diseases. Working in an international team, you will combine technical investigation, structured problem-solving and cross-functional collaboration to move device projects forward.

Your contributions will strengthen product quality, support regulatory compliance and help scale devices for the people who depend on them.

Qualifications

• A bachelor's or master's degree in engineering or related technical discipline.
• 1–3 years of relevant experience in medical devices or regulated engineering.
• Collaborative and flexible mindset with stakeholder navigation.
• Structured problem-solving approach for complex issues.
• Professional proficiency in English; Danish not required.

Responsibilities

• Contribute to medical device development and lifecycle management with internal teams and external suppliers.
• Support design control, risk management, technical documentation and regulatory compliance throughout product lifecycle phases.
• Investigate complex technical issues, identify solutions and support decisions.
• Collaborate with Quality Assurance, Regulatory Affairs, project management and supplier-facing functions.
• Participate in design reviews, risk assessments and cross-functional coordination balancing quality, patient safety, timelines and business needs.

Skills

Engineering degree

1–3 years regulatory/medical device

Collaborative mindset

Structured problem-solving

English proficiency

Education

Bachelor's or Master's in engineering

Job description

Novo Nordisk in Hillerød is seeking an Advanced Product Development Engineer to help develop and maintain medical devices that support people living with serious chronic diseases. Working in an international team, you will combine technical investigation, structured problem-solving and cross-functional collaboration to move device projects forward.

Your contributions will strengthen product quality, support regulatory compliance and help scale devices for the people who depend on them.