Regulatory Affairs Director-Full View on Product Lifecycle-CH
A fantastic director level role within regulatory affairs has come up with a leading medical device company based in the French speaking area of Switzerland. As the regulatory affairs director you will also gain management responsibility in other cross-function areas inclusive of quality, allowing you to gain a broad and varied role. Apply today to find out more to ensure you are not missing out on your next career step with a top regulatory affairs director role.
As the regulatory affairs director in this role your responsibilities will include but will not be limited to managing and leading the international registration process of globally marketed medical devices, from class I through to class III. What makes this role unique and interesting is the great deal of cross-functional work you will gain in this position; allowing you to be part of the full product life cycle. As the regulatory affairs director you will also work with the quality department, to ensure successful audits and the setting up the QMS system. You will also be in charge of a team in this role, being the key mentor within the department.
WHAT ARE WE LOOKING FOR?
You must come from a strong regulatory affairs background within the medical device industry. You will have excellent expertise within the registration process and technical documentation of medical devices on a global scale. You must have excellent knowledge of ISO 13485 and 510K. You will have gained exposure to QMS and quality assurance. You must speak fluent English and French to apply.
ENSURE you apply today for this fantastic regulatory affairs role, with a leading medical device company where you will gain a role that is varied, broad and interesting.
Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on email@example.com 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.
KEY WORDS: regulatory affairs director, regulatory affairs manager, regulatory affairs, quality assurance director, quality assurance manager, quality assurance, medical devices, switzerland, registration, ISO 13485, nonstop recruitment, medical device jobs
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