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Location:
Oxford
Salary:
Hidden
Recruiter:
TEC Partners
Job Hours:
Full-time
TEC Partners is pleased to have partnered with a pioneering medical device company who is set to pave the way for AI-based automated analysis software to overcome a global crisis affecting millions of lives.
Quality and Regulatory Specialist
As the Quality and Regulatory Specialist, you will play a pivotal role in my client's mission to deliver groundbreaking solutions in global diagnostics.
Your key responsibilities will include document control and the ability to implement robust document control processes while working closely with the Head of Quality and Regulatory Affairs establish the QMS aligned with ISO requirements, driving continuous improvement and operation excellence.
The successful candidate will also compile technical files with comprehensive documentation to support regulatory submission and product certification while conducting risk management activities in accordance with ISO , identifying potential hazards, assessing risks and implementing effective mitigation strategies.
Quality and Regulatory Specialist Key Responsibilities:
Quality and Regulatory Specialist Requirements:
This is an exciting opportunity to be part of a dynamic and innovative company dedicated to making a meaningful impact on the lives of millions affected by diabetes.
If you are driven by excellence, passionate about regulatory compliance, and eager to contribute to the future of healthcare, the Head of Quality and Regulatory Affairs is driven to help you develop your career with a clear pathway set to develop up to a managerial level.
If you're interested, please apply with an up to date CV as this role will not be available for long.
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