DHF - Akt. Med Dev

Baden-Württemberg  ‐ Vor Ort
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Schlagworte

Support Rapid Test Design

Beschreibung

Devise History File Consultants
An innovative and market leading Medical Devices company is currently looking for Devise History File Consultants to take on an initial 8 month contract ASAP.

The Consultants will support and review Design History Files for conformance to applicable requirements.

They should review and define:

- Clear design inputs

- Outputs and verification

- Sample sizes

- Test method Validation

- Gaps versus regulationsand will provide rapid resolutiontogaps

Requirements:

- Minimum 5 years med dev experience

- Design control experience (CFR part 820.30) necessary

- FDA, ISO and med dev directive experience necessary

- Experience with active med dev products preferred

- Experience with med dev products class III preferred

- 8 months with possible Extension

- Start date: May 2016

- Business fluent in English

- German is not required

- Baden-Wurttemberg, Germany

If you are interested please apply with an updated version of your CV in English and we will contact you shortly.

As the company is looking for multiple consultants, please do not hesitate to contact suitable friends and colleagues!

Key Words: Medical Device, Device History File, CFR Part 820.30, Test Method Validation, FDA, ISO

Mehr Informationen über Real Staffing erhalten Sie unter www.realstaffing.com/de
Start
05/2016
Von
Real Staffing
Eingestellt
08.04.2016
Projekt-ID:
1106439
Vertragsart
Freiberuflich
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