Associate Manager, Regulatory Affairs (Hybrid)

Work Flexibility: Hybrid**What you will do-**- Coordinate the annual submission plan for new product registrations and renewals, aligning plans with COFEPRIS requirements and contributing to their development.Also, responsible for handling specific or challenging demands.
- Lead and manage a team of three individuals overseeing medical equipment regulatory submissions to COFEPRIS in Mexico.
- Conduct monthly meetings with AMID and engage with regulatory affairs counterparts in other Latin American countries, the US, and production facilities.
- Oversee the regulatory submission process for medical devices, ensuring compliance with COFEPRIS guidelines and maintaining contact with manufacturing plants.
- Collaborate cross-functionally to align regulatory strategies with product development and commercial goals, ensuring adherence to regulatory standards.
- Participate in the creation and enhancement of regulatory submission plans, adapting to evolving regulatory re...