A global health technology company is seeking a Senior Regulatory Affairs Specialist to support innovative IVD solutions in EMEA. The role involves managing product registration projects, working closely with regulatory and commercial teams. With over 5 years of experience in the life sciences industry, you will handle regulatory documentation, ensure compliant market access, and actively contribute to product registrations. Fluency in English and strong project management skills are crucial for this position. Join a dynamic team dedicated to shaping healthcare innovation.
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