Senior Medical Device Verification Engineer

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

Job summary

Novo Nordisk A/S in Denmark seeks an Advanced Test Engineer to plan, execute and document design verification for medical devices and primary packaging. You will work with project teams to ensure products meet requirements and regulatory expectations through robust testing, delivering reliable, patient-focused devices.

You will join Device Verification Development in Hillerød, collaborating across Development, Manufacturing, Quality Assurance and Regulatory Affairs.

Qualifications

• Degree in Biomedical, Mechanical or Pharmaceutical Engineering, or another relevant scientific or technical discipline.
• Experience planning, coordinating and reporting testing or verification activities within product development projects.
• Strong analytical skills, with the ability to interpret complex data and communicate findings clearly.
• Excellent written and verbal communication skills in English.
• The ability to collaborate across functions and build strong stakeholder relationships.

Responsibilities

• Lead design verification testing and shelf-life studies across development projects.
• Develop, review and execute test protocols, analyse results and communicate conclusions to stakeholders.
• Define and support verification strategies that ensure product requirements are verified throughout the development lifecycle.
• Drive continuous improvements in test methods, processes, tools and ways of working.
• Collaborate with specialists and project teams across product development, quality, manufacturing and regulatory functions.

Skills

Design verification planning

Data analysis

Communication

Collaboration

English proficiency

Education

Biomedical/Mechanical/Pharmaceutical Engineering degree

Job description

Novo Nordisk A/S in Denmark seeks an Advanced Test Engineer to plan, execute and document design verification for medical devices and primary packaging. You will work with project teams to ensure products meet requirements and regulatory expectations through robust testing, delivering reliable, patient-focused devices.

You will join Device Verification Development in Hillerød, collaborating across Development, Manufacturing, Quality Assurance and Regulatory Affairs.