QMS Auditor - MedTech manufacturer - Switzerland
QMS Auditor - ISO 13485/ MedTech manufacturer - Switzerland - German and English essential
What with a timeline in place for compliance to ISO 13485-16 and the MDR, there is a consistent demand for seasoned QA professionals with auditing experience to ISO 13485/QMS within the Medical Devices sector. Certified Lead Auditors preferred but not essential. A working knowledge of ISO 13485 is essential - ISO 9001, FDA equivalents, and at times GMP also.
Our current requirement is with a Medical devices manufacturer in Switzerland, however we are regularly having similar needs in Germany.
Good written and spoken English mandatory, German essential.
Travel does form an inherent part of this position.
For more information on this vacancy, please contact the Senior Consultant Andrew Boroky on 0041 43 50 80 816, and email him your resume in WORD format to email@example.com. For industry news and new opportunities in QA within the Medical Devices sectors, please join my Linked group at ch.linkedin.com/in/qaswitzerland/en
KEY WORDS: Quality Management, QA, QMS, Quality Management System, Quality Assurance, Supplier quality, Risk Management, Compliance, CAPA, process optimization, Medical Devices, Switzerland, Germany, Austria, ISO 13485, ISO 9001, GMP, Medical Device jobs, Training, Nonstop recruitment, Manufacturing, Engineering,
NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.