We are currently working on a Senior Supplier QA auditor for a global client who specialises within the medical device field.
Due to continued development and within their business they are looking for an individual to conduct audits of the suppliers and third party manufacturers across the globe to access compliance to all applicable standards, regulations and internal Quality System requirements.
The role will also participate in audits of manufacturing and commercial affiliated sites, be involved in various projects across the group that will be cross functional and cross divisional and act as the leading subject matter expert.
Our client is looking for the successful candidate to be degree education, have a minimum of 5 years working within either the medical device, pharma or other heavy regulated environment. You will also need to have a strong understanding of GMP, Quality systems standards and regulatory requirements such as 21 cfr 820, ISO13485 and IVDD.
This role will required extensive travel of upto 50% and will require the individual to be happy and able to work independently.
This is an excellent opportunity for an experience auditor to join a dynamic and driven business.