São Paulo, São Paulo, Brazil
PharmD, fluent in English; Expressive career of more than 15 years in technical area of GxP multinational companies Quality & healthcare compliance, medical communication and product safety; Crisis and Ethical Interactions Committee; Qualified person, Lead Auditor, regulatory affairs, risk management; Deep knowledge in Interfarma code of conduct, RDC 96/2008 (Drug Advertising), KPIs and Power BI; knowledge in clinical research; Project and People Management (leader coach, teamwork, people development). Passion in promoting excellence in customer service, helping to find business opportunities and best practices. Dedicated and organized professional with solid analytical abilities, effective communication and negotiation skills, works independently, watchful on details and learning agility. Looks for business opportunities/risks and collaborate to determine solutions for identified gaps. Solid Academic Education: B.A. in Biochemistry Pharmacy - PharmD (USP) Lato-sensu Postgraduate studies in Quality and Productivity (USP) M.B.A in Marketing (USP) Specialization in: Professional development in clinical research (Invitare) Advanced Management in Clinical Trials (Cepic). Pre- and post-marketing Pharmacovigilance (Racine) Leader Coach (IBC) Regulatory Affairs and Registration of Drugs (Racine) Contact email: [email protected]
(Ended after maternity leave) Technovigilance/adverse events, complaints CAPA, change control, audit/inspection, SOPs, trainings, business improvement projects
(Temporary) Business support related to healthcare compliance and excellence Review of Promotional and non promotional materials, medical interactions and events SOPs, training, AI, medical process facilitation
Quality culture project Quality system management (training, CSV, quality compliance, SOPs, risks, data integrity, audit/inspection, Quality Management Review) Regulatory Intelligence