Lead Medical Device Development Engineer

Eurofins; Cambridge; On-site; GBP 70,000 - 110,000; Full time

Benefits offered by this job

Health plan

Pension plan

Life assurance

Employee assistance programme

Perkbox

Free on-site parking

Volunteer days

Job summary

Eurofins is seeking a Device Development Lead to drive cross-functional medical device development projects, overseeing the full lifecycle from concept to industrialisation. The role requires coordinating with internal and external partners to deliver on quality, time and budget targets.

The candidate will contribute to human factors studies, usability programs, and regulatory submissions while maintaining high standards of quality and compliance in a fast-paced environment.

Qualifications

• Degree in Chemical Engineering or related scientific/engineering discipline; pharmaceutical development knowledge desirable.
• Strong understanding of GxP and regulated environments with quality-focused approach.
• Excellent communication and relationship-building skills; able to work with internal and external stakeholders.

Responsibilities

• Lead multidisciplinary medical device development projects with technical leadership and mentorship.
• Manage full device development lifecycle from concept through design control and validation.
• Support human factors/usability studies and contribute to product development programmes.
• Contribute to complaint investigations, design change control and regulatory submissions.
• Support supplier assessments and preparation of technical documentation for compliance.

Skills

Chemical Engineering

GxP/regulatory

Problem solving

Communication

Organization

IT skills

Team collaboration

Education

Degree in Chemical Engineering

Tools

Microsoft Office

Job description

Eurofins is seeking a Device Development Lead to drive cross-functional medical device development projects, overseeing the full lifecycle from concept to industrialisation. The role requires coordinating with internal and external partners to deliver on quality, time and budget targets.

The candidate will contribute to human factors studies, usability programs, and regulatory submissions while maintaining high standards of quality and compliance in a fast-paced environment.