Description
This consultant would be brought on board to carry out the following tasks;- Technical file reviewing and writing
- CE marking of new products
- Product submissions, for Europe,USA,Canada,Australia,Japan,China.
- Maintaining and implementing change to the Quality Management System.
- Influencing the set up of a new QMS.
Essential Experience.
- Strong working experience within medical devices.
- Proven working experience within Regulatory Affairs & Quality Procedures mentioned above.
- Medical devices are electro mechanical respiratory devices, so specific device experience and experience of 60601 would be preferred but not essential.
The client is based aroundMaidstoneand looking to pay between £40-50 per hour depending on experience and is looking to interview over the next few weeks.
If you believe you have the correct experience for the role then please forward me your CV and I will be in touch shortly.
Alternatively if you know someone who is suitable we offer £200 worth of vouchers to anyone who refers a candidate that we place.
Look forward to hearing from you.
To find out more about Real please visit www.realstaffing.com