MedTech Software Engineer — Regulated Device Production

Cure Talent Ltd; East Midlands; On-site; GBP 50,000 - 70,000; Full time

Job summary

Cure Talent Ltd partners with an innovative medical technology company developing a complex hardware and software-based medical device. We are seeking a Software Engineer to help transition research software into production-quality medical device software.

You will collaborate with hardware, systems and scientific teams, bringing practical experience of regulated software development and helping establish robust processes around requirements, traceability, risk management, verification and

Qualifications

• Degree in Software Engineering, Computer Science or related field.
• 3+ years of commercial software development experience in a product development environment.
• Experience with C++, Object Pascal/Delphi, or Python/C#/C.
• Practical experience in regulated product development, ideally medical devices.
• Experience with requirements, traceability, risk management, testing and V&V.
• IEC 62304 and/or ISO 13485 experience would be advantageous.

Responsibilities

• Design, develop and maintain production-quality software for complex medical technology.
• Help transition existing research software into robust, compliant medical device software.
• Develop software interfacing with hardware, instrumentation and data acquisition systems.
• Contribute to requirements, design controls, traceability, risk management and technical documentation.
• Plan and execute software verification and validation activities, including unit and integration testing.
• Help strengthen and mature software development processes within a regulated environment.

Skills

C++

Object Pascal/Delphi

Python

C#

C

Regulated software development

Requirements tracing

Education

Degree in Software Engineering or Computer Science

Job description

Cure Talent Ltd partners with an innovative medical technology company developing a complex hardware and software-based medical device. We are seeking a Software Engineer to help transition research software into production-quality medical device software.

You will collaborate with hardware, systems and scientific teams, bringing practical experience of regulated software development and helping establish robust processes around requirements, traceability, risk management, verification and