Regulatory affairs Medical Devices Contract - Remote work. A few days work and then 1 day a week until 2020 -REMOTE working

On Application
19 Nov 2018
19 Dec 2018
Remote Devices
Regulatory Affairs
Contract Type

We have a client with a need for a medical device expert for the following project:

Countries covered: 

•RU + CIS: RU, BY, KZ, UA (4)

•LATAM: BR, MX, CO, CL, PE, EC, PA, VE, AR, GT (10)

•Asia: CN, VN,; JP, KR (South Korea), MY, TH, ID (Indonesia), IN, SG (Singapore), TW (Tajvan), KW (Kuwait), AE, SA (Saud-Arabia), QA (Katar), IL (Izrael), BH (Bahrein), OM (Oman), IQ (Irak), IR (Iran), YE (Jemen), HK (Hongkong), PH (Republic of the Philippines), SG (Singapore), LA (Laosz), MM (Mianmar) (25)

•Australia: AU; (Partneres) NZ (New Zeland) (2)


•Africa: ZA, DZ (Algeria), TN (Tunesia), MA (Morocco), EG (Egypt), NG (Nigeria), NG (Kenya), UG (Uganda) (8)1. Registration requirements in all countries for class IIB Report - 

2. Submission Planning and Strategy - 

3. Registration Execution - 

The time would be a few days work from Dec - March and then one day a week until end of 2020. The role is remote and the hourly rate will be £50. The product that needs registration already has its CE marking.

Key skills / key skill:regulatory affairs , regulatory affairs, regulatory , reg affairs , regulatory , medical devices , CE Marking , LATAM. CIS

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