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Regulatory Affairs Consultant Medical Devices £55 - £60ph NW
Eingestellt von Real Staffing Group aus Frankfurt am Main
Gesuchte Skills: Consultant, Support
Projektbeschreibung
Medical devices client in thenorth westis looking for a senior regulatory affairs consultant for the development, verification, validation of, and post-market support for, in vitro companion diagnostic medical devices.
You will be responsible for joint project team global regulatory operations and company-wide clinical consultancy.
Regulatory submissions US and EU: pre-IDE, MAF, IDE, PMA, Technical Files
Clinical affairs and regulatory compliance
Sole responsibility for FDA Bioresearch Monitoring (BIMO) inspection
Support for FDA PAI (quality) audit
You MUST have experience with the above and extensive regulatory affairs experience within medical device companies.
Regulatory Affairs Consultant Medical Devices £55 - £60ph Immediate Start
Please contact Steven Ruddy from Real Pharma - Medical Devices on 0207 758 7322To find out more about Real please visit www.realstaffing.com
Projektdetails
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Einsatzort:
North West England, Vereinigtes Königreich
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Organisation/Management, Sonstiges