My client is one of the leaders in the development and manufacture of medical devices for Orthopaedic applications and with operations in over 50 countries! They are looking for experienced individuals in regulatory affairs within medical devices experience to join their growing team as a regulatory specialist. This opportunity is a great chance to gain international experience career progression.
As a regulatory specialist your role will be to develop and update design dossiers and technical files in accordance to regulations set out. My client mainly focuses on class III products and as such you will gain great experience. You will also be involved in risk management and working with cross functional teams to develop project plans. Due to your duties, experience in medical devices regulatory affairs is essential for you to be able to fulfil your role.
You will be a part of an expanding company who have recently opened a new site and are looking for specialists to make sure everything is up to scratch. This opportunity is great for you develop your experience both on an international level in the industry and also with the
high standard of device you will be working with.
Please contact Andrew Boroky at Nonstop Medical Devices for a confidential discussion about this or any other of our current positions either by phone on +44 207 940 2116 or email me at email@example.com
Posted: 15/08/2012 | NPJ Ref: 85092