Introduction

My client is a innovative medical devices company based in Scotland . They are aiming to change the face of many healthcare sectors including Oncology and Cardiology. They are expanding their teams an looking for a Quality engineer to join their team

This role will offer you:

• Flexible working start and finish times
• Opportunity to part of a rapidly expanding medical devices company
• Other benefits such as a bonus and medical insurance

You will be responsible for:

• Compiling regulatory submissions and technical files for new and existing products
• Provide ongoing regulatory guidance and ensure compliance with relevant regulatory requirements
• Support post market surveillance and vigilance activities
• Develop internal regulatory policies and procedures and provide training as required
• Participate in company regulatory/quality audits

You will bring the following:

• Experience of working with quality and regulatory standards including ISO13485
• 2 years experience in Regulatory affairs within the medical devices industry
• International regulatory experience with awareness of EU MDD/MDR, FDA, health Canada and other regional regulations
• Bachelor of science degree in biology or similar field

If you want to be part of an exciting company where you can grow and expand your current knowledge, GET IN TOUCH by emailing me on isaac.murray@biotalent.com