Beschreibung
Experis is part of the Manpower Group
"Validation Engineer/GMP/CFR/Compliance"Experis seeks multiple "Validation Engineers" to join an international team with a prestigious leading company in Zuchwil, Switzerland.
Main tasks:
The Validation Engineer has to execute review and propose remediation of historical validation records associated with equipments ensuring that all compliance issues and requirements of the Clients Validation Policies and Procedures are addressed.
Requirements:
- In-depth knowledge of 21 CFR 820, 21 CRF 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 progressed experience is needed
- 2-5 years working in a regulated industry a minimum 2 of wich has been spent carrying out validations
- Pure Consultants profile will be preferred
- Must be able to work on multiple sim,ultaneous tasks with limited supervision
- Communication and Team-Collaboration skills are highly welcomed
- Language proficiencie in English, German is a strong advantage.
Start Date is planned for ASAP, latest 1.11.2013
Next Steps:
Are you feeling suitable and are interested in this Solothurn based project, then please send your CV immediately to Mirco In-Albon. Gladly we have more information available; you can reach me via telephone. Please follow up with a call upon applying for this role.
Experis has a large global client portfolio which enables us to offer multiple employment positions on the local Swiss and Global markets. Experis offers equal employment opportunities and support cultural diversity.
Apply to us now for your next contracting role; we look forward to hear from you.