Specialists in Pharma, Clinical & IT Recruitment

Regulatory Affairs Specialist

Reference:
RAS1
Job Type(s):
Regulatory Affairs
Salary:
Salary negotiable
Benefits:
Excellent Benefits
Town/City:
Manchester
Contract Type:
Permanent
Date Posted:
21/01/2014 11:42:00
Start Date:
21/01/2014
End Date:
19/03/2014

Description

My client an International Medical Device company has opened a new vacancy within their Regulatory Affairs team. They are actively looking to hire a Regulatory Affairs Specialist to join their team on their offices on a permanent basis in Manchester.

Key Responsibilities:

·         Ensuring compliance with global regulatory requirements

·         Participation in project teams to provide regulatory input into cross departmental

International registration projects

·         Preparation of documentation in order to support Global regulatory

·         submissions

·         Review and approval of labelling, advertising and promotional materials in

·         order to ensure regulatory compliance

·         Supporting Post-Market Surveillance and Vigilance activities

 

 

Position requirements, qualifications and experiences:

·         Minimum scientific degree (or equivalent) in life sciences

·         Experience in a similar role within the medical device industry,

(Preferably in vitro diagnostics). Working knowledge of the MDD and

IVDD, applicable ISO standards and US medical device/IVD regulation

·         Good interpersonal and communication skills

·         Ability to handle multiple projects simultaneously

·         Ability to work with minimal supervision

 

For more information regarding this vacancy or a confidential job discussion, please get in touch with Neal Panting. Neal@arc-7.com or +441483 397070

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