Work Flexibility: Hybrid
**What you will do**
- Ensure compliance of products with local norms and maintain updated product records.
- Validate product registration lists and update Stryker's regulatory tools.
- Manage local licenses and execute the Registration Plan across all franchises.
- Represent Stryker at COFEPRIS for submissions and collection of resolutions.
- Monitor regulatory changes through associations and technical committees.
- Authorize advertising materials and support post-marketing surveillance reporting.
- Provide regulatory and documentary support to Quality, Tenders, Operations, and Sales.
- Lead continuous improvement activities in regulatory processes.
**What you need**
**Required**
- Bachelor's Degree.
- Minimum 2 years of experience in regulatory processes in a medical device industry.
- Advanced/Conversational English skills.
- Intermediate knowledge of Microsoft Office.
- Knowledge in sanitary regulation on Healthcare's company.
- Ability to use tools and resources related to product registration.
**Preferred**
- Quality assurance knowledge.
Travel Percentage: 10%