Validation Engineer - Solothurn, Switzerland

Vertragsart:
Vor Ort
Start:
ASAP
Dauer:
keine Angabe
Von:
Templeton and Partners
Ort:
Solothurn
Eingestellt:
05.10.2013
Land:
flag_no Schweiz
Projekt-ID:
608968

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Validation Engineer - Solothurn, Switzerland

Required skills:

In depth knowledge of 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry

High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations

Medical devices experience is needed, minimum of 2 - 5 years working in a regulated industry a minimum 2 of which has been spent carrying out validations.

Validation Engineer to execute review and propose remediation of historical validation records associated with equipment ensuring that all compliance issues and requirements of the clients Validation Policies and Procedures are addressed.