Design Engineer -Medical Devices

Euro London Appointments; Twickenham; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading recruitment agency is seeking a Design Engineer to join a growing biomedical devices company in Twickenham. The role involves designing medical devices, managing design documentation, and conducting usability studies. Candidates must have an engineering degree and at least 2 years of experience in the medical devices field. Fluency in English and understanding of ISO-13485 is essential. Competitive salary based on experience.

Qualifications

• Minimum 2 years in an engineering role within medical devices.
• Good understanding of reporting requirements under MDR/ISO-13485.
• Minimum 2 years in an engineering role within medical devices.
• Must be fluent in written and spoken English to C1 level.
• Good understanding of MDR/ISO-13485 reporting requirements.

Responsibilities

• Design support in the product design of new medical device products.
• Managing design documentation in accordance with ISO 13485 and FDA Quality Management System.
• Conduct usability studies and incorporate user feedback into design improvements.
• Lead design control and risk management activities; conduct risk assessments and implement corrective actions.
• Perform usability studies and incorporate user feedback into designs.
• Foster strong relationships with internal and external stakeholders.

Skills

Electronic or Electrical Engineering

Fluent in written and spoken English (C1 level)

Understanding of MDR/ISO-13485

Risk management

Usability studies

Education

Degree in Electronic or Electrical Engineering

Tools

CAD software

Programming

IT networking

Job description

Overview

We have an exciting new role for a Design Engineer to form part of an innovative and growing Biomedical Devices company. You will be joining an experienced team with the vision to grow the business worldwide. You will have the opportunity to bring new technology to new regions.

Responsibilities

• Design support in the product design of new medical device products.
• Managing design documentation in accordance with ISO 13485 and FDA Quality Management System.
• Providing support to manufacturing and post-sales activities as required. Some travel to customer sites.
• Facilitate effective design control and risk management activities both internally and with external partners. Conduct risk assessments and identify potential design flaws. Conduct root cause analysis and implement corrective actions for design issues.
• Conduct usability studies and incorporate user feedback into design improvements.
• Develop and maintain good working relationships with key internal and external stakeholders.

Qualifications

• Degree in Electronic or Electrical Engineering is essential.
• Minimum 2 years in an engineering role within medical devices.
• Must be fluent in written and spoken English to C1 level.
• Good understanding of reporting requirements under MDR/ISO-13485.

Desirable

• Experience with CAD drawings.
• Programming.
• IT networking.

Additional information

• Location: Twickenham, London, United Kingdom.
• Salary: dependent on experience.
• Right to work: It is essential to have full right to work status for the UK on a long-term basis; sponsorship is not available.
• Application notes: CVs will be treated in confidence; only applicants whose profiles match the client requirements will be contacted.

Seniority

• Associate

Employment type

• Full-time

Job function

• Engineering and Design

Industries

• Engineering Services
• Medical Equipment Manufacturing