About the Role:
For my client, an innovative Medical Device Company, based in the Zürich Area, i am looking for a Medical Device- QA Documentation Specialist for the following responsibilities:
- Review of Test Protocols, Test Reports, TMT documents, Design documents, Master Validation Protocols, V&V Reports
- content review, making sure that the documents are in good standardised quality
- Data Record analysis (NC, complaints, supplier corrective actions, etc.)
- Creation of Templates
- Implement new reports, writing SOPs
- 2-5 years working experience in Medical Devices (ISO 13485, FDA & MDD)
- Documentation Experience
- Experience in reviewing of technical document's in the Medical Device industry
- Experience with reporting and creation of different reports
- English must, German is nice to have
- Very good excel knowledge
- European passport
The project start is end of April beginning of May, with a project duration of 2-3 months, with potential extension.
If you are interested in working in an innovative environment based in Zürich, being able to take your own responsibility's, then this might be the perfect short assignment for you.
I am looking forward hearing from you until Tuesday 18/03 and if possible, please update your CV according to the job requirements in order to increase your chance for a an interview.
Senior Candidate Relationship Manager
Medical Devices Pharma & Biotech
Real Ein Geschäftszweig der SThree GmbH Talstrasse 65