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Job Description

My client is looking for a QA/RA Contractor to support them from the beginning of December on their product currently undergoing clinical trials on an ad-hoc basis (2/3 days per week)

Essential Skills:

Medical device Regulatory affairs experience in CE/UKCA marking.

Provide regulatory input to functional groups as required.

Perform Technical Documentation File reviews prior to submission for registrations

Review of RA procedures for compliance

ISO 13485 Audit Support

Desirable skills:

Able to help develop US regulatory strategy.

Able to help gain ISO 13485 Accreditation.

The Role:

Remote

Outside IR35

40 per hour

If this is of interest please send over a CV.

Please visit our website to find out more about our Key Information Documents. Please note that the documents provided contain generic information. If we are successful in finding you an assignment, you will receive a Key Information Document which will be specific to the vendor set-up you have chosen and your placement.

Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy