JOB TITLE: Regulatory Affairs Manager


Industry : Commercial & Finance Job Location : Essex
Job Reference : 6826SR Job Category : Pharmaceuticals
Employment Type : Permanent Posted : 16/07/2010
 
Salary & Benefits : £35000 - £55000 per annum
 
Experience Required : See Job Description
 
Education Required : See Job Description



Please note you must be permitted to work in the EC to apply for this job.

Job Summary

Bluefire Consulting are recruiting for an experienced Regulatory Affairs Manager to work within a busy Manufacturing QA/RA department in our client's offices in Southend-on-Sea, Essex.


Job Description

Bluefire Consulting are recruiting for an experienced Regulatory Affairs Manager to work within a busy Manufacturing QA/RA department in our client's offices in Southend-on-Sea, Essex. Main duties will involve:

* Leadership of the Regulatory Affairs team to ensure compliance with regulations
* Liaising with external authorities and internal contacts on relevant regulatory matters
* Overseeing all product registration, reportable medical device incidents and field safety corrective actions
* Establishing, maintaining and managing the complaints handling system
* Supporting and liaising the manufacturing division on all regulatory matters
* Ensuring products and systems comply with worldwide regulations


Previous experience within a Regulatory Affairs position within a medical manufacturing environment is essential for this role. A degree, or equivalent, in a science-related discipline is required for this role. The successful Regulatory Affairs Manager must be able to demonstrate accuracy, attention to details and strong interpersonal skills.


Job Keywords

Regulatory Affairs Manager; Essex; Medical; Manufacturing



Bluefire Consulting is an equal opportunities Employment Business/Agency specialising in Pharmaceuticals recruitment on a UK wide basis.

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