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Vanessa Rivel

Vanessa Rivel has 15 years of experience in the medical device sector. Her background includes regulatory affairs, quality systems, auditing, and training. Currently, she works as an independent consultant. Her past work experience includes roles as a Quality Systems Engineer at Hospira, Quality Transfer Engineer at Boston Scientific, Site Quality Manager at  Sterigenics, and Quality Systems Manager at Precision Concepts Group. She has completed her Meng in Industrial Engineering and MBA In Marketing and Licentiate in Chemistry. She holds a certificate for Regulatory Affairs Certified (RAC), Certified Lead Auditor ISO 13485 (Exemplar Global), Certified Manager of Quality / Organizational Excellence (ASQ), Certified Quality Engineer (ASQ), Certified Six Sigma Green Belt (ASQ), Medical Device Master Auditor (ASQ), and Certified Quality Auditor (ASQ),

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