Beschreibung
Experis is part of the Manpower Group
"Validation Engineer/FDA/CFR/"Experis seeks multiple "Validation Engineers" to join an international team with a prestigious leading company in the beautiful cantons of Basel and Solothurn, Switzerland.
Main tasks:
Project Quality Support in the CSV Equipment Legacy Review
Project Quality Support in CSV Equipment Remediation Projects Tasks:
Cover the part of the GxP-Compliance in the project.
Creation of the Validation documentation for GxP relevant system elements.
Know and follow the guidelines regarding the code of conduct, ethics and compliance programs and other relevant regulations
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 and German is a must
Start Date is planned for ASAP, latest 15.4.2014
Next Steps:
Are you feeling suitable and are interested in this Solothurn based project, then please send your CV immediately to Simon Alexander. 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.