Vanisha Mistry-Ngumbau

Vanisha Mistry-Ngumbau has a wealth of work experience. Vanisha began their career in 2007 as an R&D Engineer at Orthomimetics Ltd. In 2010, they held the role of Ink Lab Technician at Tonejet Limited and Project Co-ordinator at Sagentia. From 2012 to 2018, they were a Non-Active Medical Device Lead Auditor - Technology Auditor at TÜV SÜD Product Service - UK. During this time, they also held the roles of Quality Lead- Supply Chain Assurance and Senior GMP Auditor at Mundipharma International Limited. In 2018, they became Director at SAVERINE QUALITY CONSULTANTS LIMITED. In 2021, they were a Regulatory Consultant at Cerina and Head Of Compliance at Cydar Medical.

Vanisha Mistry-Ngumbau attended the University of Nottingham from 2004 to 2007, where they earned a BSc in Biomedical Materials Science. Prior to that, they attended West Island School from 1999 to 2002.