Description
My client, a leading medical device company is seeking a Supplier Quality Engineer. You will join the company's quality management systems department with approximately 20 employees at the moment.This 6 month contract carries the following responsibilities:
- Execution of supplier analysis
- Support and consulting for the development of corrective action plans and corrective actions at suppliers
- Evaluation and monitoring of corrective actions at suppliers
- Support for the evaluation of new products at suppliers as well as new suppliers
- Collaboration with the purchasing departments regarding scheduling and communication with suppliers
- Maintenance of the supplier database
- Optimization of the supplier structure
To convince the company about your profile you should have the following expertise:
- Expert understanding of FDA CFR Part 820, Part 11, and ISO 13485 regulations is required
- A Bachelor or Master degree in a related science or engineering field
- Business fluency in German and English is required
- Expertise in dealing with the FDA and other regulatory bodies is preferred
- Proven skills and knowledge in quality related methods and techniques, auditing principles
- Knowledge and skills in quality-related methods and techniques including auditing principles and techniques, quality terminology, as well as quality management principles and quality management tools and their applications are preferred
- Travel commitment is required
For more information on this role please roles within related specialist areas apply immediately to Marcus Müller at Real Pharma Zurich. I look forward to your application.
Keywords: supplier quality, medical device, qms, freelance/temporary, FDA CFR 820/11, 13485, supplier analysis, Switzerland, travel, German, English
<p>To find out more about Real please visit <a href="http://www.realstaffing.com">www.realstaffing.com</a></p>