Description
Due to plans to expand into new markets this exciting and highly intelligent business now needs a Regulatory Specialist to aid the completion of 510k submissions and product registrations.They are a consumer based, over OTC Medical Device Company in the Home Counties, currently searching for a Regulatory affairs specialist for a 3 Month contract, to help speed up a growth program by assisting in multiple 510k submissions, and Product Submissions in the far east.
Working closely with the RA/QA manager, the successful individual will be completing regulatory activities that are essential for the business to move in to a possible two new territories.
Contractors Responsibilities Include;
*Completing current 510k submissions to the FDA for Electro Mechanical Devices.
*Working on Product Submissions to Japan & Korea.
*Regulatory Writing & Filling.
*Advising on general Regulatory activity.
Essential Experience;
*3-5+ experience in Medical Devices
*Must have proven tract record of product submissions and registrations.
*Must have Dealt with 510k's before.
*Experience working with products that fall under rd edition, is preferable but not essential.
*Availability must be no more than 3 weeks.
The client is looking to pay from £ 33-37 Per hour and this role is full time for 3 months.
There is also flexibility for working from home on this role 3 days per week.
If you believe you have the correct experience then please email me your up to date CV and I will be in touch shortly, or contact Joseph Dykes on .
I have Interview slots for this role for later this week, so move fast to avoid disappointment.
To find out more about Real please visit www.realstaffing.com