New-Gen


Functional Experience: Consulting Services; Logistics, Transport Industry Experience: Biotech, Health Science, Pharma.; Biotech, Health Science, Pharma.
Job: 003598	REGULATORY ENGINEER, MEDICAL DEVICES – MIDLANDS \| 2010-02-25
Company:	NonStop _Recruitment
Country:	United Kingdom
State:	Londonderry
City:
Professional Level:	Analyst/Consultant
Employment Type:	Full-time / Permanent
Compensation Level:	45000 per Year United Kingdom, Luton, 40000.00 - 45000.00 United Kingdom Pounds/Year
Choice of how resumes arrive:	Microsoft Word Microsoft Excel
Job
# Description MEDICAL DEVICES, REGULATORY AFFAIRS SPECIALIST – NEW PRODUCT REGISTRATION AND PRODUCT MAINTENANCE!! IF YOU HAVE A BACKGROUND IN MEDICAL DEVICES REGULATORY AFFAIRS & COMPLIANCE – APPLY NOW!!! Senior Regulatory Specialist – Engineering & Compliance; suitable candidates to have a registrations, standards & compliance planning and post marketing surveillance background. Experienced in the preparation of dossiers and maintenance, you will possess a minimum 4 years regulatory experience with worldwide medical device registrations. Specifically, you will have: MDD 93/42/EEC and FDA QSR 21 CFR part 820 Regulations, or other equivalent systems. A highly competitive package is on offer for the appropriate candidate. Can you afford to miss this rare and superb Regulatory Affairs opportunity in a very sought-after location? For a confidential discussion and to find out more information about this Regulatory role or any other Regulatory Affairs roles please contact our Senior Regulatory Manager Julian Turner on the Regulatory Affairs Team on 0207 234 0550 or by e-mail to Regulatory@NonStop-pharma.com
Required Skills & Experience # Ideal candidate Regulatory, Medical Devices
Pre-application questions: NO