Lead Vigilance
hace 3 días
A healthcare technology company based in Galicia, Spain is seeking a Regulatory Affairs Specialist to ensure compliance with medical device reporting requirements. Responsibilities include serving as the local contact with Spanish authorities, managing vigilance processes, and supporting audits. Candidates should have relevant experience in medical writing and complaint processing, along with a BA/BS degree. Fluency in Spanish and English is essential. This dynamic role involves collaboration across various functions to maintain regulatory compliance.
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Lead Vigilance and QARA Spain
hace 3 días
Ourense, España Insulet Corporation A tiempo completoPosition OverviewReview, analyze, and compose responses to regulatory agencies regarding medical device reportable events and collaborate both within post market surveillance and across other functions, including customer care, quality, clinical and regulatory to help ensure compliance with reporting requirements and good documentation practices. This...