Regulatory Affairs Associate, Medical Devices - Spain

A leading life sciences organization in Spain is seeking an experienced Regulatory Affairs Specialist to manage regulatory impact assessments, annual registrations, and global submissions, particularly to the FDA. The ideal candidate will have a Bachelor's degree and a minimum of 4 years of experience in Regulatory Affairs within the medical device sector. Strong communication and problem-solving skills are essential, and fluency in English is required. This position offers a unique opportunity to collaborate with global partners and contribute to compliance and timely submissions.
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