Description
My client, an innovative and growing start-up Medical Device company is seeking an adaptable and experienced Regulatory Affairs Specialist to join their team for a six month contract on a part time basis. The Regulatory Specialist will work a 2-3 day week and an attractive daily rate is on offer.As Regulatory Affairs specialist you will be responsible for preparation of product registration files for submission to global regulatory bodies/agencies, to support EU CE Marking, FDA, and foreign regulatory submissions, in order to obtain product approvals and maintain regulatory compliance with international regulatory requirements. Reviewing and evaluating technical and scientific data and reports and incorporating them into documents for submission to the EU, FDA and foreign regulatory agencies will also be an integral part of your role.
While working as Regulatory Affairs Specialist you will be responsible for all regulatory submissions and preparation of internal reports and change control documents.
Requirements:-Bachelors Degree in engineering or equivalent/4-5 years regulatory experience in the medical device industry
This is an urgent requirement interviews will take place immediately. If you are interested in gaining a wealth of Regulatory and Medical Device experience in a company where no one is pigeon hole to one specific area or task, please contact me Anna Mooney or apply below with an up to date CV.
To find out more about Real please visit www.realstaffing.com