3 of 3 Permanent Regulatory Compliance Jobs in Oxfordshire

Medical Device Embedded Software Engineer

Hiring Organisation
Talent STEM Ltd
Location
Littlemore, Oxfordshire, United Kingdom
Employment Type
Permanent
Salary
GBP Annual
devices. Working closely with hardware, systems and quality teams, you will contribute across the full development lifecycle from requirements through to testing, validation and regulatory compliance. You will also help improve development processes, support system integration and contribute to the continuous improvement of engineering standards aligned with medical device … regulations and quality systems. Key Responsibilities - Design, develop and maintain embedded software for medical devices - Support requirements definition and software architecture in line with regulatory standards - Implement and verify firmware for embedded platforms used in medical systems - Support hardware bring-up, integration and debugging activities - Develop test and support

Medical Device Embedded Software Engineer

Hiring Organisation
Talent STEM Ltd
Location
Hybrid, Littlemore, Oxfordshire, United Kingdom
Employment Type
Permanent
devices. Working closely with hardware, systems and quality teams, you will contribute across the full development lifecycle from requirements through to testing, validation and regulatory compliance. You will also help improve development processes, support system integration and contribute to the continuous improvement of engineering standards aligned with medical device … regulations and quality systems. Key Responsibilities - Design, develop and maintain embedded software for medical devices - Support requirements definition and software architecture in line with regulatory standards - Implement and verify firmware for embedded platforms used in medical systems - Support hardware bring-up, integration and debugging activities - Develop test and support

Medical Device Embedded Software Engineer

Hiring Organisation
Talent STEM Ltd
Location
Florence Park, Oxford, Oxfordshire, England, United Kingdom
Employment Type
Full-Time
Salary
Salary negotiable
devices. Working closely with hardware, systems and quality teams, you will contribute across the full development lifecycle from requirements through to testing, validation and regulatory compliance. You will also help improve development processes, support system integration and contribute to the continuous improvement of engineering standards aligned with medical device … regulations and quality systems. Key Responsibilities - Design, develop and maintain embedded software for medical devices - Support requirements definition and software architecture in line with regulatory standards - Implement and verify firmware for embedded platforms used in medical systems - Support hardware bring-up, integration and debugging activities - Develop test and support