in Regulatory Affairs within the life sciences or medical industry.
• Strong understanding of international regulatory frameworks (e.g. FDA, MDR, ISO 13485, MDSAP).
• Proven success managing portfolios across multiple projects and geographies.
• Effective...
Identify circularity data needed for mandatory and voluntary disclosures globally' and develop and manage workstream to improve quality of and access to data' in collaboration with appropriate DT' Government Affairs' Global Sustainability and Brand teams...