Software Test Engineer - Medical Devices
Posted on Jul 22, 2026 by CV-Library
Manchester, Greater Manchester, United Kingdom
IT
Immediate Start
£400 - £425 Daily
Contract/Project
Role: Embedded Software Test Engineer - Medical Devices (V&V)
Contract length: 6 months (initially)
Location: Manchester - 3 days per week onsite
Rate: Up to £425 per day, Outside IR35
We're recruiting a Software Test Engineer (V&V) for our client, an innovative medical device company based in Manchester currently progressing a market-ready device through FDA 510(k) approval. Following a recent scope increase in testing and documentation requirements, they need an experienced V&V engineer to take full ownership of test activity as the sole test resource on site.
This is a hands-on, standalone role. You'll be working directly with the device hardware, so onsite presence three days a week is essential. This cannot be done remotely.
Key Responsibilities
Develop verification and validation test specifications from the device's design history file, requirements and specifications
Break high-level design/ test requirements down into detailed sub-tests, test protocols and expected outcomes
Execute and record verification/validation testing in line with relevant standards and processes
Feed results back to the development team and support resolution of any non-conformances
Design software test plans in compliance with IEC 62304 and FDA documentation standards
Instrument and execute unit, module, integration and regression tests based on software design specifications
Work closely with Quality and Regulatory colleagues to ensure testing supports the technical fileSkills & Experience required:
Strong experience of V&V activities within an embedded software environment
Embedded software development background using C/C++, sufficient to understand and define module-level tests
Experience converting requirements into structured test cases and procedures
Experience working with medical devices running embedded software
Working knowledge of IEC 62304 and ISO 13485
Good understanding of the full software engineering lifecycle
Able to work independently and self-manage a standalone testing functionDesirable
Knowledge of IEC 60601 and/or ISO 14971Contract Details
6 month initial contract, with potential to extend
3 days per week onsite in Manchester
Up to £425 per day, Outside IR35How to Apply
If you have embedded software V&V experience within a regulated medical device environment and IEC 62304 / ISO 13485 knowledge, apply now or contact Chris Oddy to discuss further
Contract length: 6 months (initially)
Location: Manchester - 3 days per week onsite
Rate: Up to £425 per day, Outside IR35
We're recruiting a Software Test Engineer (V&V) for our client, an innovative medical device company based in Manchester currently progressing a market-ready device through FDA 510(k) approval. Following a recent scope increase in testing and documentation requirements, they need an experienced V&V engineer to take full ownership of test activity as the sole test resource on site.
This is a hands-on, standalone role. You'll be working directly with the device hardware, so onsite presence three days a week is essential. This cannot be done remotely.
Key Responsibilities
Develop verification and validation test specifications from the device's design history file, requirements and specifications
Break high-level design/ test requirements down into detailed sub-tests, test protocols and expected outcomes
Execute and record verification/validation testing in line with relevant standards and processes
Feed results back to the development team and support resolution of any non-conformances
Design software test plans in compliance with IEC 62304 and FDA documentation standards
Instrument and execute unit, module, integration and regression tests based on software design specifications
Work closely with Quality and Regulatory colleagues to ensure testing supports the technical fileSkills & Experience required:
Strong experience of V&V activities within an embedded software environment
Embedded software development background using C/C++, sufficient to understand and define module-level tests
Experience converting requirements into structured test cases and procedures
Experience working with medical devices running embedded software
Working knowledge of IEC 62304 and ISO 13485
Good understanding of the full software engineering lifecycle
Able to work independently and self-manage a standalone testing functionDesirable
Knowledge of IEC 60601 and/or ISO 14971Contract Details
6 month initial contract, with potential to extend
3 days per week onsite in Manchester
Up to £425 per day, Outside IR35How to Apply
If you have embedded software V&V experience within a regulated medical device environment and IEC 62304 / ISO 13485 knowledge, apply now or contact Chris Oddy to discuss further
Reference: 225399522
https://jobs.careeraddict.com/post/113590811
Software Test Engineer - Medical Devices
Posted on Jul 22, 2026 by CV-Library
Manchester, Greater Manchester, United Kingdom
IT
Immediate Start
£400 - £425 Daily
Contract/Project
Role: Embedded Software Test Engineer - Medical Devices (V&V)
Contract length: 6 months (initially)
Location: Manchester - 3 days per week onsite
Rate: Up to £425 per day, Outside IR35
We're recruiting a Software Test Engineer (V&V) for our client, an innovative medical device company based in Manchester currently progressing a market-ready device through FDA 510(k) approval. Following a recent scope increase in testing and documentation requirements, they need an experienced V&V engineer to take full ownership of test activity as the sole test resource on site.
This is a hands-on, standalone role. You'll be working directly with the device hardware, so onsite presence three days a week is essential. This cannot be done remotely.
Key Responsibilities
Develop verification and validation test specifications from the device's design history file, requirements and specifications
Break high-level design/ test requirements down into detailed sub-tests, test protocols and expected outcomes
Execute and record verification/validation testing in line with relevant standards and processes
Feed results back to the development team and support resolution of any non-conformances
Design software test plans in compliance with IEC 62304 and FDA documentation standards
Instrument and execute unit, module, integration and regression tests based on software design specifications
Work closely with Quality and Regulatory colleagues to ensure testing supports the technical fileSkills & Experience required:
Strong experience of V&V activities within an embedded software environment
Embedded software development background using C/C++, sufficient to understand and define module-level tests
Experience converting requirements into structured test cases and procedures
Experience working with medical devices running embedded software
Working knowledge of IEC 62304 and ISO 13485
Good understanding of the full software engineering lifecycle
Able to work independently and self-manage a standalone testing functionDesirable
Knowledge of IEC 60601 and/or ISO 14971Contract Details
6 month initial contract, with potential to extend
3 days per week onsite in Manchester
Up to £425 per day, Outside IR35How to Apply
If you have embedded software V&V experience within a regulated medical device environment and IEC 62304 / ISO 13485 knowledge, apply now or contact Chris Oddy to discuss further
Contract length: 6 months (initially)
Location: Manchester - 3 days per week onsite
Rate: Up to £425 per day, Outside IR35
We're recruiting a Software Test Engineer (V&V) for our client, an innovative medical device company based in Manchester currently progressing a market-ready device through FDA 510(k) approval. Following a recent scope increase in testing and documentation requirements, they need an experienced V&V engineer to take full ownership of test activity as the sole test resource on site.
This is a hands-on, standalone role. You'll be working directly with the device hardware, so onsite presence three days a week is essential. This cannot be done remotely.
Key Responsibilities
Develop verification and validation test specifications from the device's design history file, requirements and specifications
Break high-level design/ test requirements down into detailed sub-tests, test protocols and expected outcomes
Execute and record verification/validation testing in line with relevant standards and processes
Feed results back to the development team and support resolution of any non-conformances
Design software test plans in compliance with IEC 62304 and FDA documentation standards
Instrument and execute unit, module, integration and regression tests based on software design specifications
Work closely with Quality and Regulatory colleagues to ensure testing supports the technical fileSkills & Experience required:
Strong experience of V&V activities within an embedded software environment
Embedded software development background using C/C++, sufficient to understand and define module-level tests
Experience converting requirements into structured test cases and procedures
Experience working with medical devices running embedded software
Working knowledge of IEC 62304 and ISO 13485
Good understanding of the full software engineering lifecycle
Able to work independently and self-manage a standalone testing functionDesirable
Knowledge of IEC 60601 and/or ISO 14971Contract Details
6 month initial contract, with potential to extend
3 days per week onsite in Manchester
Up to £425 per day, Outside IR35How to Apply
If you have embedded software V&V experience within a regulated medical device environment and IEC 62304 / ISO 13485 knowledge, apply now or contact Chris Oddy to discuss further
Reference: 225399522
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