Experienced Cross Regional Regulatory Professional

Johnson & Johnson MedTech

São Paulo, Brazil
**
Regulatory requirements
Life cycle management
Submission dossier assembly
** Johnson & Johnson MedTech is seeking an Experienced Cross Regional Regulatory Professional in São Paulo, Brazil, to support regulatory activities for its product portfolio. The role involves collaboration with regional teams, ensuring compliance with regulatory requirements, and contributing to the development and management of submissions. **

Job Summary

  • Provides support to regulatory activities for products in the assigned portfolio, including development, post-approval, and life cycle management.
  • Works with regional staff and Local Operating Companies to support regional and local activities and assists in preparing meetings with Regulatory Agencies.
  • Responsible for the critical review of submission documents to ensure compliance with regulatory requirements and provides regulatory support for inspections, audits, and product complaints.

Matching Summary

Match Score: 75

** Johnson & Johnson MedTech is seeking an Experienced Cross Regional Regulatory Professional in São Paulo, Brazil, to support regulatory activities for its product portfolio. The role involves collaboration with regional teams, ensuring compliance with regulatory requirements, and contributing to the development and management of submissions. **

Skills & Requirements

Must-have

  • regulatory requirements
  • life cycle management
  • submission dossier assembly
  • regional regulatory strategy
  • Health Authority interaction

Nice-to-have

  • customer focus
  • intellectual curiosity
  • sense of urgency
  • collaboration and teaming
  • adaptability

Key Requirements

  • 2 years relevant experience
  • B.A./B.S. in science/relevant health-related discipline
  • Excellent English verbal and written communication skills

Work Rights

Not specified

Tailored Resume

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