£25,000 - £35,000 per annum
Closing Date: 18/11/2020
A rare and exciting opportunity has arisen for a Regulatory Affairs Associate based in Falmouth on a permanent basis.
If you are from a strong administrative, medical devices, regulatory or quality background we would love to hear from you!
Joining a friendly team and reporting to the Regulatory Affairs Executive you will be responsible for:
- Compiling and maintaining the Technical Documentation Files
- Plan and execute audits to identify gap analysis
- To lead on submissions for new Medical Devices
- To coordinate the review and documentation of intended uses for each product
- To inform and educate internal partners of new and revised EU regulatory standards
- Being the main regulatory point of contact for product and process risk management
If you have knowledge of the national and international medical device regulatory requirements this would be beneficial but full training will be given to someone with the right aptitude and willingness to learn.
You must be a fast learner, possess strong administration skills. A background in bio-science, regulatory or quality would be ideal but not essential.
In return the company are offering a salary from £25,000 to £35,000 DOE.
Hours are 8am to 4:30pm Mon to Thurs and 8am to 3:30pm on Friday's.
To find out more about this fantastic and rare opportunity please call Sally at the Truro branch of Berry Recruitment for more information.
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