Clients - 07837903599 / 07900246876
Candidates - 07966706060

Engineering - 07957676291

admin@stemrecsolutions.co.uk

An exciting opportunity has arisen for a talented Regulatory Affairs professional to join a global medical device manufacturer based in Livingston. As part of the regulatory team you will support the international registration of products in various markets.

The main duties include:

·Preparing, maintaining and submission of European and global registrations, technical files and CE Marking.
·Ensuring regulatory requirements are met for all markets where products are sold and proactively keep abreast of new regulatory requirements and standards.


·Assessing the regulatory impact of product and process changes.
·Developing regulatory strategies for new or changed products and processed including initial European submission and the global roll out in accordance with the business strategy ad objectives for the business.
·Liaising with regulatory authorities and customers as necessary during the regulatory submission process.
·Assisting in the gathering of metrics and improvements to regulatory processes.

The successful candidate will have previous experience within a medical device environment, have a relevant scientific degree with a fundamental understanding of EU and other regulatory requirements. They will be a strong communicator with good interpersonal skills and the ability to interact with all levels within the organisation and externally.

Please apply online in the first instance.

Follow Us

Call Us

Clients - 07837903599 / 07900246876
Candidates - 07966706060
Engineering - 07957676291
admin@stemrecsolutions.co.uk

 

STEM Recruitment Solutions is the trading name of STEM Recruitment Solutions Ltd. A1 Avondale House, Pheonix Crescent, Strathclyde Business Park, Bellshill, ML4 3NJ

Registered Company No. SC526261 / VAT Registration No. 239790074