Senior MedTech Engineer & PM Lead (Onsite NL)

Medtronic; Geleen; On-site; EUR 87,000 - 131,000; Full time

Benefits offered by this job

Medtronic Incentive Plan (MIP)

Flexible benefits

Job summary

Medtronic Articulating Technologies in Geleen, Netherlands, seeks a Principal Engineer to lead complex medical-device development projects from concept through commercialization, blending deep engineering expertise with program management.

You will mentor engineers, coordinate across Quality, Regulatory, Manufacturing, Clinical and Commercial teams, and ensure safe, regulatory-compliant product delivery in a fast-paced, cross-disciplinary setting.

Qualifications

• Master’s degree in Mechanical Engineering, Biomedical Engineering, Industrial Engineering or similar.
• >7 years proven experience managing complex projects or programs in research and product development in the medical device industry.
• Experience with product and process development aligned with ISO 13485 requirements.
• Strong analytical and problem-solving skills with attention to detail.
• Fluent in Dutch and English.

Responsibilities

• Act as senior technical authority for medical device development across projects.
• Develop and review system architectures, requirements, design concepts and documentation.
• Provide mentorship and day-to-day direction to engineers.
• Lead cross-functional projects with plans, schedules, budgets, and milestones.
• Represent Engineering in cross-functional and executive meetings.
• Collaborate with Quality, Regulatory, Manufacturing, and Commercial teams to translate needs into robust technical solutions.

Skills

Leadership

Program management

Analytical thinking

Dutch & English

Education

Master’s degree in Mechanical/Biomedical/Industrial Engineering

Job description

Medtronic Articulating Technologies in Geleen, Netherlands, seeks a Principal Engineer to lead complex medical-device development projects from concept through commercialization, blending deep engineering expertise with program management.

You will mentor engineers, coordinate across Quality, Regulatory, Manufacturing, Clinical and Commercial teams, and ensure safe, regulatory-compliant product delivery in a fast-paced, cross-disciplinary setting.