Compliance and Regulatory Officer
Biotechnology Chemical Clinical Life Sciences Pharmaceuticals
An exciting opportunity has become available for a technical compliance and regulatory officer, with a leading medical devices organisation.
In the role you will be responsible for preparing medical device manufacturing documentation, and validation reports. Ideally you will be experienced with technical specification documentation which supports medical device manufacturing process and design transfer, and have a comprehensive understanding of design controls, risk management processes and QMS.
An understanding of the principles of design for manufacture, MDD and MDR, and knowledge of document management systems would be highly desirable.
This is an exciting role where you will be liaising with internal and external colleagues globally.
If you have a background regulatory and QA compliance relating to medical device manufacture then you would be well suited to the requirements of this role.