Job title: Regulatory Affairs Specialist

A global pharmaceutical business in the Southwest is seeking a Regulatory affairs Specialist to join their growing team. This role requires someone with experience working with Medical devices or food supplements.

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 or Food supplements 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