
This week we welcome Claire Spalding to the Enteral Access Technologies™ team. Claire has a demonstrated history of working in the medical device industry and has a reputation for quality assurance. She is taking on the role of the DoubleCHEK™ Regulatory & Quality Specialist.
Claire has over 15 years of experience as a quality and regulatory professional, predominantly in Medical Device and chemical manufacturing fields. She has lead multi-disciplinary and multi-site quality compliance projects, including the global harmonisation of document control and quality system consolidation to achieve ISO 13485 certification. Key strengths include quality systems improvement, CAPA, document control, audits, and driving culture change.
Claire’s overall mission is to ensure that the quality function drives continuous improvement and maximises efficiency.