Daniel Bouchard
About Daniel Bouchard
Daniel Bouchard is a Safety Manager at Groupe Rocher, where he has worked since 2016. He has extensive experience in toxicology and safety management, having held various positions in organizations such as FAREVA, Horiba Jobin Yvon, and INERIS.
Work at Groupe Rocher
Daniel Bouchard has been serving as the Safety Manager at Groupe Rocher since 2016. In this role, he leads a team of five professionals focused on safety management. His responsibilities include overseeing the safety evaluations of raw materials, fragrances, and packaging. Bouchard's expertise ensures that product safety assessments meet regulatory standards and consumer safety expectations.
Previous Experience in Toxicology and Project Management
Before joining Groupe Rocher, Daniel Bouchard held various positions in the field of toxicology and project management. He worked at FAREVA as the Toxicology Director from 2014 to 2015 and as the Regulatory Affairs Director / Toxicologist in Global R&D from 2011 to 2013. Additionally, he served as a Project Manager at Horiba Jobin Yvon in 2011 and at ESPCI ParisTech from 2009 to 2010. His experience includes a research role at INERIS from 2006 to 2009.
Education and Expertise
Daniel Bouchard's educational background includes a PhD in Toxicology from Université Paris Cité, which he completed from 2006 to 2009. He also holds a Master of Science in Environment and Health from the same institution, achieved in 2003. His earlier studies include a B.Sc. in Biochemistry from both Université Henri Poincaré, Nancy 1 and Lebanese University - Faculty of Sciences. Additionally, he has a Certificat in Epidemiology and Biostatistics from Université Saint-Joseph de Beyrouth.
Certifications and Professional Standards
Daniel Bouchard holds EUROTOX certification, which underscores his expertise in European toxicology standards. This certification is indicative of his proficiency in the field and his commitment to maintaining high professional standards in toxicological assessments. His work involves overseeing in vitro, in vivo, and clinical testing processes as part of comprehensive safety assessments.