Have a background in Regulatory Affairs in Medical devices?
Looking for a career move with a company that values it employees with flexible working?
Looking for an uplift in your salary? (£Excellent)
*Our client is a Medical Devices business, supplying a wide range of medical products into global markets.
*Business growth combined with the organisations commitment to further reinforce its market leading status, has created an exciting opportunity for a Regulatory Affairs Senior Specialist or Manager.
· Support regulatory submissions for approval to regulatory authorities worldwide. · Maintain current registrations, licenses, Regulatory Certification, and submissions to ensure compliance with the latest regulations. · Compile and maintain Technical Files. · Support other functions within the business for information requests, review of artwork and other literature · Review and approval of key compliance records (e.g. Labelling and instructions for use) for all sites. · Participate in company quality system, audits.
*Science or engineering based degree or equivalent qualification, experience of working in the medical devices industry would be essential. Ideally my client is looking for a self -driven individual, with strong communication skills.
*Regulatory Affairs experience - minimum 5 years.
*You must be authorised to work in the UK.
Expion: Our healthcare manufacturing recruitment brand is well respected for the high quality of work we have delivered for both clients and candidates. Our in-depth knowledge of manufacturing recruitment across core sectors enables us to provide expert advice based on experience and to give you the best access to blue chip client vacancies.
To apply for the role, please send your CV and salary details to Expion Search & Selection using the 'Apply Now' button. If you would like to have a confidential discussion on the role, you can contact the Consultant, Richard Clegg.