Regulatory Affairs & Quality Specialist-Global Role-Devices-CH
Work within global regulatory affairs and quality assurance today with this fantastic role as a regulatory affairs and quality specialist. The global market is an exciting place to work, especially with the developing emerging markets. This opportunity will give you the invaluable expertise to develop as a regulatory affairs and quality professional across all markets. Thus leading to an exciting role but also fantastic future job prospects. Apply now to find out more!
As the regulatory and quality specialist in this role your responsibilities will include but will not be limited to:
- You will be working on the full product life cycle, allowing you to be part of all the processes and develop your expertise from start to finish.
- Develop the QMS and audit system with the director of regulatory affairs and quality.
- Work on an international scale, where you will develop key expertise in some of the most exciting and growing emerging markets.
The ideal candidate for this role will come from a quality and regulatory background within the medical device industry. You will have good working knowledge of ISO 13485 and have worked on an international scale. You are fluent in both English and German.
We look forward to hearing from you today if you are ready to take on a fantastic role that will take your regulatory affairs and quality career to the global platform.
Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on firstname.lastname@example.org or +41 435 0808 16, please send your CV in word format OR if this does not sound like the opportunity for you, but you are a regulatory affairs professional within the medical device industry, please feel free to get in touch, to see other opportunities we may have within this field.
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