Regulatory Documentation Associate

hace 2 días


San José, San José, Costa Rica Zimvie A tiempo completo
Key Responsibilities
  • Coordinate and assist in the preparation of technical documentation for use in regulatory submissions worldwide.
  • Assist with research, analysis and communication of information pertaining to the appropriate regulatory pathway for new or modified products.
  • Aid in regulatory direction to development project teams as a core team member; supports regulatory strategy for new products.

This role requires strong writing, communication, and interpersonal skills, as well as the ability to work effectively in a dynamic environment.



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