Senior Regulatory Affairs Lead – Medical Devices (Spain)

A leading medical device firm in Spain is seeking a Senior Staff Regulatory Affairs Specialist. You will support product development, ensuring compliance with regulatory standards and leading cross-functional projects. This role requires at least 7 years of experience in regulatory affairs within the medical device sector and fluency in English, Spanish, and Portuguese. You'll contribute significantly to regulatory strategy, assess risks, and drive process improvements in a dynamic environment.
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