QA Documentation / QMS Specialist / French Swiss site
Ours is a Swiss Company developing innovative medical products for the dental sector, world wide. These are exciting times as the company grows, and with it a need for specialised staff. In the role of QA Documentation Specialist, you are part of a team responsible for document management processes, change management and training.
Daily tasks will be to
- develop materials and provide training linked to the quality management system
- monitor process improvement and the performance of the document management processes
- evaluate and process change requests
- Support the QA department wrt QM System
A suitable background: 1-3 years experience in a similar position in the medical devices, pharmaceutical or biotechnology industry, and an excellent knowledge of ISO 13485 and 21 CFR 820
Attention to detail, good analytical skills, a good knowledge of Quality Management Systems, and proficiency in MS Office environment.
The role will be based in French Switzerland, and with the QMS in both English and French, French is essential to be successful in this role
For a confidential discussion of this exciting new position, please contact Andrew Boroky on +41 43 50 80 816 or by e-mail to email@example.com and send in a WORD copy of your resume together with scanned copies of your Arbeits Zeugnisse and training certifications.
For industry news and new opportunities in QA generally within the Medical Devices & Diagnostics sectors, please join my Linked group ch.linkedin.com/in/qaswitzerland/en
KEY WORDS: Documentation, Quality Assurance, QA, Compliance, SOP, Auditor, Medical Devices, Switzerland, ISO 13485, ISO 9001, GMP, ISO 14971, CAPA, Medical Device jobs, nonstop recruitment.
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