Austin Vita has been engaged by an industry-leading Medical Devices business to find a Regulatory Specialist to support their growing Regualtory Affairs team on a 6 month contract basis.

Responsibilities:

* Aid in the delivery of clients registrations strategy in compliance with the MDR

* Minimise the time it takes for products to hit the market

* Identify EU and US regulatory requirements and ensure they are implemented across the business for the full lifecycle of the product

* Technical File Remediation and preparation of documents for 510k Submissions

* Process EMEA Product Submissions

To be considered for this position you must have a minimum of 5 years experience working in an ISO 13485 regualted environment and be knowledgeable in the process of global product submissions.

If the position is of interest, please get in touch.

Austin Fraser is acting as an Employment Business in relation to this vacancy.

Austin Fraser is committed to being an equal opportunities employer, and encourages applications from candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity status.

Due to the volume of applications received, we are unable to provide individual feedback to unsuccessful applicants.