**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, General 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 completo
Sueldo: Hasta $21,000.00 al mes
Beneficios:
- Vales de despensa
Pago complementario:
- Bono anual
Tipo de jornada:
- Turno de 8 horas
Lugar de trabajo: Empleo remoto

📌 Regulatory Affairs Analyst (México)
🏢 Genomma Lab México S.A. de
📍 México