- Experience Level
- Experienced (non-manager)
Exciting Medical Device/Regulatory opportunity with an established company!
2 years experience in Regulatory Affairs/Medical Devices?
Seeking opportunity with the chance of career progression and work in over 50 countries worldwide?
Get in touch today!
My client is an established, global supplier of Medical technology for critical care, operating theatre and home healthcare applications and supply products in over 50 countries worldwide. Their mission is to provide high quality innovative products to patients and caregivers around the world. The success of the company has been built on continuous innovation, excellent customer service and an inherent commitment to improving the quality of life of patients.
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
More information available on request.
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