Found Description
Join Roche as an International Regulatory Affairs Professional to drive regulatory solutions for global IVD/MD instruments and software. Bring your expertise in regulatory strategy, compliance, and cross‑functional collaboration to impact patient care worldwide.
Todas las habilidades, cualificaciones y experiencia relevantes que necesitará un candidato seleccionado se enumeran en la siguiente descripción.
Key Responsibilities
- Lead and support regulatory strategies for global IVD/MD instrument and software submissions.
- Ensure compliance with international regulatory requirements and standards.
- Collaborate with cross‑functional teams (R&D, Quality, Clinical) to drive regulatory initiatives.
- Provide regulatory guidance to support product development and lifecycle management.
- Stay abreast of evolving regulatory trends and implement best practices.
Requirements