Development Engineer

ZipRecruiter; Cambridge; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading medical technology business is seeking a Lead Development Engineer for a 6-month temporary contract in Cambridge. The role involves producing high-quality CAD designs, conducting development analyses, and ensuring compliance with regulatory standards. Applicants should have a degree in Mechanical Engineering or Product Design and strong CAD skills, with medical device experience being highly desirable.

Qualifications

• Minimum 2:1 degree qualification in Mechanical Engineering or Product Design.
• Proficient in creating detailed 3D CAD models and drawings.
• Experience in medical device design and development is highly desirable.
• Skills in testing, validation, and regulatory documentation.
• Ability to work effectively across teams and with external partners.

Responsibilities

• Produce high-quality CAD designs for device parts and test equipment.
• Plan and conduct development analyses and empirical tests.
• Perform data analysis, interpretation, and reporting.
• Write and review specifications, validation documents, and risk management files.
• Apply regulatory standards such as ISO 13485 and ISO 14971.
• Support internal teams and external partners with technical expertise.
• Drive improvements to processes, documentation, and compliance.

Skills

Strong CAD experience

Problem-solving skills

Analytical skills

Communication skills

Collaborative approach

Education

Degree in Mechanical Engineering or Product Design

Job description

Overview

We are working with a leading medical technology business in their search for a Lead Development Engineer to join their Device Development team in Cambridge. This is a 6-month temporary contract, with a strong likelihood of extension, offering the chance to contribute to the development of innovative, patient-focused medical devices.

Responsibilities

• Producing high-quality CAD designs for device parts and test equipment
• Planning and conducting development analyses and empirical tests
• Performing data analysis, interpretation, and reporting for manufacturing and technical areas
• Writing and reviewing specifications, validation documents, and risk management files
• Applying regulatory standards such as ISO 13485, ISO 14971, and 21 CFR 820.30
• Supporting internal teams and external partners with technical expertise
• Driving improvements to processes, documentation, and compliance within the development function

About you

• Degree qualified in Mechanical Engineering or Product Design (2:1 minimum)
• Strong CAD experience – proficient in creating detailed 3D models and drawings
• Proven experience in medical device design and development is highly desirable
• Skilled in testing, validation, and regulatory documentation
• Excellent problem-solving and analytical skills
• Collaborative approach with strong communication skills
• Able to work effectively across internal teams and external partners

This is an excellent opportunity for a skilled engineer to contribute to life-changing medical technologies within a highly respected business. Apply today for immediate consideration!