3 of 3 Regulatory Compliance Jobs in Oxfordshire

Senior Trust Assurance Specialist

Hiring Organisation
DigiCert
Location
Oxford, Oxfordshire, UK
Employment Type
Full-time
Senior Trust Assurance Specialist to join the Trust Office team at DigiCert. The successful candidate will have at least 5 years of experience in compliance, risk management, and leading internal and external audits, with a strong background in ISO 27001, ETSI, and other relevant cybersecurity standards. This role requires … individual with a strong knowledge of regulatory frameworks, exceptional analytical and organizational skills and the ability to effectively communicate and collaborate with internal and external stakeholders. The role will report to DigiCert's Head of Compliance and will be part of the Trust Office team What you will ...

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 ...