Job title: Regulatory Affairs Associate

A global pharmaceutical business in the Southwest is seeking a Regulatory affairs Associate to join their growing team. This role requires someone with experience working with medical devices.

Responsibilities:

Responsible for the maintenance and QC of product information.
Responsible for life cycle management of products in the UK and EU, with further maintenance of global products
Responsible for Quality Management System activities and authoring of QMS documentation
Cross-functional collaboration to provide regulatory advice and strategy

Requirements:

Previous Medical device experience.
Experience in dealing with UK and EU authorities.
Proven experience of working with cross-functional teams.
Ability to develop and implement regulatory strategies.

Salary and benefits:

A competitive salary and benefits package is on offer for this role.

To apply for this position or hear further details then please contact Freddie Hill via Freddie.hill@pharma-partners.co.uk