Regulatory Affairs Specialist to Nobel Biocare in Göteborg
Proffice Sverige AB / Kemistjobb / Göteborg
2008-01-18
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hela Sverige We are seeking a Regulatory Affairs Specialist
This position as Regulatory Affairs Specialist involves to ensure that the regulatory work of Nobel Biocare is handled in a correct and effective way so that only products approved by regulatory expertise approved products are available on the market. The Regulatory Affairs Specialist will work in an international environment with authorities, officials and agencies within Europe, Americas, Asia-Pacific and report directly to the Global Director Clinical & Regulatory Affairs Department.
Responsibility:
The primary responsibilities of this position involve preparations of product registrations to regulatory authorities globally, serve as regulatory advisor for design teams and contributing regulatory expertise to research products.
You will continuously investigate and keep yourself updated on requirements related to global product approvals, develop Regulatory Plans, maintain and update regulatory registrations, approval processes, standards and changes on a daily basis.
For this challenging position within Nobel Biocare we are looking for someone that has a relevant exam and background. The person should have a few years of regulatory experience within medical device business.
As a person you need to be flexible and able to make priorities. You can take on large responsibilities, you are service minded by nature and a good team member but can work independently as well. Other key factors we are looking for are excellent communication skills and fluent in English and one other language except Swedish.
Publiceringsdatum2008-01-18Anställningstyp/arbetstiderTillsvidare
KontaktAnefors, Sofie
Så ansöker duAnsök via vår webbplats »
To apply, upload you CV and personal letter at
www.proffice.se . For further information please contact Sofie Anefors 031-807645.
Sista ansökningsdag 2008-02-03
FöretagProffice Sverige AB
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Jobbnummer 103639
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