Regulatory Affairs Analyst

**ROLE DESCRIPTION**- Lead the compilation and review of technical documents for products spanning food, drugs and cosmetics.
This will involve collaboration with regulatory consulting firms, external suppliers, as well as internal functions - Global Regulatory, Global Quality, Global R&D, US Commercial, US Brand, US Supply.- Maintain electronic repositories for technical dossiers to ensure they are properly named, sorted and stored.- As directed by project needs, share documents & dossiers with key stakeholders - both internally and externally.
**PROFESSIONAL PROFILE (**_**Education, Experience, Technical Knowledge, Companies and / or Categories preferences**_**)**- Undergraduate degree or diploma in a science-related field - for example, biology, chemistry, pharmacology, biotechnology or microbiology.- **2+ years**of professional experience in a corporate, academic or government environment- Ability to manage multiple projects/priorities while maintaining high quality output- Proficient in MS Office (Powerpoint, Excel, Word, etc.
).- Keen interest and/or demonstrated proficiency in electronic document & data management, especially cloud-based repositories.- Proficient across multiple communication platforms - for example, WhatsApp, Microsoft Teams.Tipo de puesto: Tiempo completoSueldo: Hasta $21,000.00 al mesBeneficios:- Vales de despensaPago complementario:- Bono anualTipo de jornada:- Turno de 8 horasLugar de trabajo: Empleo remoto