Introduction

An exciting opportunity has arisen to work for one of the worlds largest medical device notified bodies.

The role will offer you:

• fully remote working from anywhere within Germany
• Extensive training courses
• opportunity to work with a variety of different medical devices
• opportunity to improve understanding of how wound care companies do things
• flexible working hours

You will be responsible for:

• performing onsite audits at manufacturers premises in accordance with EU medical device regulations
• performing technical documentation assessments to the MDR
• conscientious compilation of reports and audit related documents
• Operating as a project handler with responsibility for the coordination and management of audit related projects

You will bring:

• Degree (or equivalent qualification) in a relevant scientific or engineering discipline
• 3-4 years experience within R&D, Testing, Design of Medical Devices at a Medical Device Manufacturer or Supplier
• Auditing experience of healthcare products
• Knowledge of QMS standards, and/or EU devices legislation
• Fluent English speak

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