Jamile Sendoda has extensive experience in regulatory affairs, beginning as a Regulatory Affairs Intern at Royton Química Farmacêutica and advancing to roles such as Regulatory Affairs Analyst at Glenmark Pharmaceuticals and Zambon Laboratórios Farmacêuticos Ltda. Jamile held senior positions, including Sr Regulatory Affairs Analyst at Sanofi and AbbVie, overseeing regulatory submissions, line extensions, and lifecycle management for biologic products and new drugs. Expertise includes compliance with local regulations, interaction with regulatory entities, and project management for labeling and artwork submissions. Academic qualifications include a degree in Pharmacy from Centro Universitário São Camilo and a postgraduate degree from Faculdades Oswaldo Cruz.
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