Regulatory Affairs Specialist - MDD support

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My key Biotech client are looking for RA Specialist support to help towards MDD by the end of 2019.The candidate must have RA Medical device experience, particularly in class lll devices. You would be supporting and working with R+D, clinical, RA and compliance teams. Role over view and day to day duties;- Working on technical files for the MDD- Supporting R+D- Working towards MDD on tight deadlines- Working on risk management files including reviewing, adding and assessing the files- Post market surveillance planning for after product launch Essential skills needed;- MDD experience- Medical device ISO13485 experience with class lll experience- Risk management experience ISO14971 Initial 2 months due to 2019 budgets but with the plan to extend into 2020ASAP startTwo stage interview process - 1 telephone and 1 skype To find out more about Real please visit www.realstaffing.comReal Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales