Charlton Morris are working exclusively with a highly innovative wound care Medical Device manufacturer who are looking for a Senior Director of Quality & Regulatory Affairs to assist with continued growth within the business.
This is a fantastic opportunity to join an expanding manufacturer within an innovative side of the wound care market.
Our client is looking for an experienced leader within the QA & RA arena, you must have EU, US and international regulatory submission experience, with a proven track record in Medical Devices. You will report to the Chairman and manage/ coach a team of 2 people within the business but also work cross functionally or in regional strategic initiatives to deliver quality solutions as well as provide Regulatory guidance on development.
Your responsibilities include developing and maintaining quality vision and strategies to drive excellence throughout the organization to ensure reliable delivery of high-quality products meeting or exceeding customer and relevant requirements.
Ideally you will be located the DACH or Benelux region.
If the above is ticking boxes and you are thinking of making a change, apply using this page or contact me via my email address below.
I look forward to speaking with you!