Description
They're searching for a passionate, ambitious individual with the following experience:5 years + experience in Regulatory Affairs
3 years + experience in Medical Device
510K submissions experience
Knowledge of Canadian Regulations
Nice to have
Knowledge of ISO 13485
21 CFR Part 820
Process Improvement
Experience with European regulations
If you are interested, please send me your resume. Alternatively, please send to anyone in your network who may be a good match.
To find out more about Real please visit www.realstaffing.com