- Member of the Leadership team; responsible for the preparation and review of registration, post-registration and renewal dossiers.- Leverage keen strategic skills through active participation in the submission plans alongside ANVISA and other international authorities, such as: INVIMA, DIGEMID, PIF (Europe), ANMAT. - Continuously strive for performance excellence through process improvement initiatives, standards development and metrics. Review and implement the standard operating procedures.- Coordinate activities regarding the control, supply and forwarding of registration documentation, the authorization of manufacturing processes and the export of products.- Harness exceptional interpersonal and cross departmental skills through liaising and supporting the R&D, quality, marketing, packaging and manufacturing departments; resolving compliance issues effectively and continuously seeking to improve processes.- Manage relationships with key stakeholders in the divisions of technical operations and quality, and across regulatory affairs, ensuring the provision of regulatory support therefore achieving strategic objectives and goals.- Develop and recommend regulatory strategies in innovation projects, site transfer and compliance. Provide sound regulatory guidance in order to support business development initiatives and sales functions.- The successful mapping and update of processes, procedures; ensuring uniformity within the departmental activities.

- Performed in-depth and thorough compliance reviews for all ingredients, product formulas and labelling; ensured that all reached applicable industry standards and regulations.- Leveraged impeccable preparative and analytical skills; reviewed and verified dossiers, as required, in the legislation and guide for ANVISA and LATAM.- Monitored regulatory developments and disseminated findings.- Developed incentives and facilitated new projects, focused on consumer needs; ensured such ventures were permitted by ANVISA.- Issued cosmetic product ingredient listings; ensured transparency and accuracy.- Offered technical support and ensured a level of consistency regarding communications with the local team located in Latam.- Supported local production and the roll out of innovations in Latam; directly participated in projects of tec transfer. - Created and implemented key management tools for the department.

- Evaluated and approved the labelling of cosmetic products; ensured transparency and accuracy regarding consumer information. - Conducted the formulation study; indicating companies INCI ingredients in alignment with the regulations of the EU, USA, Brazil, Argentina, Chile, Mexico and Andean Pact.- Evaluated the clinical and technical material used; ensured testing of product safety and effectiveness.- Provided regulatory guidance to the business development and sales divisions; verified “claims to support”. - Managed the operating licenses of the manufacturers for Latam.- Requests for documents and technical information to departments and / or companies involved with the product as needed, to prepare dossier, labelling and package inserts, complying with the requirements and regulatory requirements.