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Regulatory Affairs Specialist/Medical Devices
Eingestellt von Experis Schweiz AG
Gesuchte Skills: Engineering, Elan, Client
Projektbeschreibung
REGULATORY AFFAIRS SPECIALIST/MEDICAL DEVICES
On behalf of our client, an international company specialized in the medical devices we are looking for a GERMAN SPEAKING REGULATORY AFFAIRS SPECIALIST with previous experience in the MEDICAL DEVICE INDUSTRY.
The position is based in Oberdorf, it is a contract starting FROM JULY UNTIL END OF DECEMBER 2015, with an option to extend.
In this position the Regulatory Affairs will be responsible for supporting the Regulatory Affairs group in creation and maintenance of Technical File documentation as well as reviewing risk management documentation according to EN ISO 14971:2012 standards with respect to regulatory requirements.
YOU BRING TO THIS ROLE:
- Expertise in Regulatory Affairs, including profound knowledge of European Medical Device regulations
- Experience in Risk Management documentation for medical devices
- Minimum of 2 years work experience in medical device industry, especially in regulatory, labelling, quality or engineering area
- Very good experience working with MS Office (Word, Excel, Access, PowerPoint)
- Fluent in both ENGLISH AND GERMAN
If you got to the bottom of this job description and that you are still interested but are not quite ready to click the below apply button, why don't you phone Elodie Hanser.
Probably you know Experis as Elan IT - we have a new name now but we still have the same expertise in IT Recruitment. We are part of the Manpower group and at Experis IT we are responsible for recruitment of the best IT Specialists.
On behalf of our client, an international company specialized in the medical devices we are looking for a GERMAN SPEAKING REGULATORY AFFAIRS SPECIALIST with previous experience in the MEDICAL DEVICE INDUSTRY.
The position is based in Oberdorf, it is a contract starting FROM JULY UNTIL END OF DECEMBER 2015, with an option to extend.
In this position the Regulatory Affairs will be responsible for supporting the Regulatory Affairs group in creation and maintenance of Technical File documentation as well as reviewing risk management documentation according to EN ISO 14971:2012 standards with respect to regulatory requirements.
YOU BRING TO THIS ROLE:
- Expertise in Regulatory Affairs, including profound knowledge of European Medical Device regulations
- Experience in Risk Management documentation for medical devices
- Minimum of 2 years work experience in medical device industry, especially in regulatory, labelling, quality or engineering area
- Very good experience working with MS Office (Word, Excel, Access, PowerPoint)
- Fluent in both ENGLISH AND GERMAN
If you got to the bottom of this job description and that you are still interested but are not quite ready to click the below apply button, why don't you phone Elodie Hanser.
Probably you know Experis as Elan IT - we have a new name now but we still have the same expertise in IT Recruitment. We are part of the Manpower group and at Experis IT we are responsible for recruitment of the best IT Specialists.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Ingenieurwesen/Technik