Regulatory Affairs Manager (Medical Devices)
SRG are searching on behalf of a well established medical device manufacturer of high-quality skin protection and ancillary products for use in ostomy, wound care and single use surgical instruments. They are going through an period of unprecented growth, continuing their growth trajectory through these troubled times and Interviews are going ahead.
Reporting to the UK Head of Quality and Regulatory Affairs (QARA), the Regulatory Affairs Manager will be responsible for providing Regulatory direction and guidance in the UK.
The Regulatory Affairs Manager role is key to the success of the UK businesses regulatory and quality strategy, ensuring the development of regulatory strategies supporting New Product Development (NPD) and Notified Body communications / submissions.
To be sucessfull in you application you must have:
-Minimum 4 years' experience in a regulatory role-Considerable regulatory experience in a medical device customer driven environment- Experience in Medical Device or IVD environment working to ISO Standards and FDA CFR in a continuous improvement environment
This role would suit some one who is looking to take the first step into a management position or some one with 1-2 years of line management experience
If you would like more information about the position and company please apply or get in touch with me on email@example.com or 07729712538.
your application has been submitted
Back to job search