Regulatory Affairs Specialist
November 13
Description
• Lead and prepare RA meetings involving regulations. • Plan timelines and registration strategies. • Manage translations and legal documents. • Verify information for databases. • Support RAN's management under RA Manager instruction.
Requirements
• Bachelor’s or master’s degree. Pharmaceutical Sciences, Industrial Engineering, Biomedical Engineering, or field related experience. • 2 years of relevant experience in job offered or a similar role. • Advance proficiency in Spanish and English required (reading, writing and speaking). • Portuguese desirable. • Fluent English • Regulatory affairs experience in medical devices or pharmaceutical industry • Ability to work in matrix structured organization. • Proactive and has problem-solving skills as well as eager to learn and open to feedback.
Benefits
• Competitive Salary • Flexible Benefits Package
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