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Job Details

Quality Consultant

Company: EPM Scientific
Location: Zürich
Reference: TMMDR
Closing Date: 14 Dec 17
Type: Contract
Salary (£): 100,000+
Benefits:

Job Summary:

The Role:A Global Medical Device company that specialises in Dental Implants is seeking experienced Quality Assurance Consultants based in Zurich, Switzerland. My client is...

Requirements:

The Role:

A Global Medical Device company that specialises in Dental Implants is seeking experienced Quality Assurance Consultants based in Zurich, Switzerland.

My client is currently searching for senior consultants to work on an MDR specific project. You will be working alongside a group of highly experienced consultants, adjusting their products registration and standards to meet the new medical device regulations.  With over 3000 products in their portfolio, there is a vast scope of work lasting at least 12 months due to the level of requirements by the authorities in regards to the MDR.

Responsibilities:

–        Transition of Medical Device products from MDD to MDR regulations

–        Review and write technical file documentation for product registrations

–        Quality Improvements

Skills and Experience Required


-       Working knowledge of ISO 13485, MDD

-       Hands-on MDR experience

-       Post Market Surveillance (bonus)

-       English speaking


What this Job Offers You


-       A high-level consultancy project focusing on the most talked about topic for 2018.

-       A long secure project with the chance of an extension for a further year.

How to apply

Apply here if you are interested in this opportunity or if you would like a confidential discussion about your career opportunities please contact enquiries@epmscientific.com or phone +442037588855.

Disclaimers if necessary: Must have the rights to Work on Switzerland 


Apply for this job: Quality Consultant

Contact Information:

Address:  Head Office
Ground Floor 21 Lombard Street London
EC3V 9AH
England
Tel:  +44 (0)20 3758 8855
Website:  Visit Our Web Site

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