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Job Details

Regulatory Affairs Consultant – Medical Devices – Belgium

Company: Barrington James Clinical
Location: Belgium
Reference: FRSY11/08/OMD
Closing Date: 11 Sep 17
Type: Full Time
Salary (£): 60,000 - 80,000
Benefits:

Job Summary:

An excellent opportunity has recently arisen within a service orientated and quality driven company working with Medical Devices and In Vitro diagnostics. Due to the company growing, they now require a Regulatory Affairs Consultant to join their growing team and to expand their career within a fantastic organisation.

Requirements:

The successful candidate will:

•Provide a professional client service
•Perform various notification work in line with the RA\QA department
•Follow-up tasks assigned to them and co-ordinate tasks assigned to a small team (>5)
•Presentation support for management and board meetings
•Asist managers, dept. managers and/or unit directors
•Involved with the implementation of ISO 9001:2008 and ISO 13485:2003
•Provide training

Candidate requirements:

•A Scientific background
•3-5 project management and quality management experience (QA/RA)
•Familiarity with Medical Devices is considered an asset
•Experience in EU administration is considered an asset.
•Fluent in English (Written/Spoken)

Desired skills and competencies

•Knowledge of QA systems
•Excellent time management skills
•Ability to motivate team members
•Be able to travel in and out of the EU

This is a fantastic opportunity for Regulatory Affairs professionals with 3-5 years of experience. If you feel that this is the opportunity to progress your career, or you are eager to discuss this further, don’t hesitate to contact me for a confidential conversation on: 

Telephone: +44 (0) 1293 776644 

Email: fsayyah@barringtonjames.com

Apply for this job: Regulatory Affairs Consultant – Medical Devices – Belgium

Contact Information:

Address:  Head Office
Victoria House Consort Way Horley Surrey
RH6 7AF
England
Tel:  01293 776644
Fax:  01293 822333
Website:  Visit Our Web Site

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