- Experience Level
- Experienced (non-manager)
Seeking to hear from those with a minimum 2 years Medical Devices experience to discuss this exciting opportunity with an established, global supplier of Medical Technology.
Below is a brief description.
Purpose of role – Responsible for maintaining and supporting promotion of regulatory affairs and supporting overall regulatory compliance. The position provides and contributes to the delivery of regulatory deliverables from internal R&D (research and development) projects, contributing to provide regulatory solutions to business requirements and changes to regulatory landscape. The position provides operational regulatory input and guidance to cross functional terms, ensuring compliance MDSAP (medical device single audit programme) and other applicable global regulatory standards. Furthermore, the Regulatory Affairs Engineer is responsible for the completion of global regulatory submissions for product registrations in line for business to growth.
Reports to – Head of Quality Assurance and Regulatory Affairs
-Prepare submissions / compliance strategy documents in line with agreed timeframes.
-Support Generation and completion of technical documentation in line with agreed timeframes
-Hands on in the remediation of technical files with agreed timeframes
More information is available on request.
Applying for this role will put you in contact with Christian. Christian specializes in Regulatory Affairs and helps motivated individuals find the next stage of their career. If you are interested to hear about the range of opportunities, get in contact today.
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