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.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.
General Responsibilities Include;
- Completing current 510k submissions.
- Working on another two 510k's from start to finish.
- Regulatory Writing & Filling.
- Product registrations to the standards of the FDA,Japan, Asia PAC.
Essential Experience;
- 5+ experience Medical Devices
- Must have proven tract record of product submissions and registrations.
- Must have Dealt with 510k's before.
- Availability must be no more than 4 weeks.
The client is looking to pay from £40-47 per hour and this role is full time for 6-9 months.
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 .
To find out more about Real please visit www.realstaffing.com