Medical Device Development Engineer - 1-Year Hybrid

Novo Nordisk A/S

Hillerød

Hybrid

DKK 570,000 - 838,000

Part time

38 hours ago
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Job summary

Novo Nordisk A/S (Hillerød) invites engineers to join a temporary 12-month role focused on medical device development and lifecycle management. You will work within a multidisciplinary team, supporting design control, risk management and regulatory activities across product lifecycles.

The position seeks a degree in engineering with 1–3 years’ regulated industry experience and strong problem-solving ability. Four days in the office and one day at home are typical.

Qualifications

  • Bachelor's or master's degree in engineering or a related technical discipline.
  • Ideally 1–3 years of relevant experience in medical devices or another regulated engineering environment.
  • Professional proficiency in English; Danish is not required.

Responsibilities

  • Contributing to medical device development and lifecycle management activities in collaboration with internal teams and external suppliers.
  • Supporting design control, risk management, technical documentation and regulatory compliance throughout relevant product lifecycle phases.
  • Investigating complex technical issues, identifying possible solutions and helping the team make well-founded decisions.
  • Collaborating with colleagues across Quality Assurance, Regulatory Affairs, project management and supplier-facing functions.
  • Participating in design reviews, risk assessments and cross-functional coordination, balancing quality, patient safety, timelines and business needs.

Skills

Collaborative mindset
Structured problem-solving
English proficiency
Adaptability

Education

Bachelor's or Master's degree in engineering or related technical discipline

Job description

Novo Nordisk A/S (Hillerød) invites engineers to join a temporary 12-month role focused on medical device development and lifecycle management. You will work within a multidisciplinary team, supporting design control, risk management and regulatory activities across product lifecycles.

The position seeks a degree in engineering with 1–3 years’ regulated industry experience and strong problem-solving ability. Four days in the office and one day at home are typical.

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