Beschreibung
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.