Your responsibilities:
Preparation and updating of technical documentation of medical devices, supervision of documentation
Conducting the process of certification and registration of medical devices, including in foreign markets
Supervision of products in distribution
Creating documentation of clinical trials of medical devices, coordinating trials
Communication with authorities, experts, scientific institutions, foreign contractors on registration matters, new product development, etc.
Knowledge of legislation in the area of medical devices, keeping abreast of changes and their implications for ongoing projects
Preparation of texts for packaging materials and instructions for use, support in the preparation of marketing materials
Work with R&D and other departments on new product development
Preparation and updating of technical documentation of medical devices, supervision of documentation
Conducting the process of certification and registration of medical devices, including in foreign markets
Supervision of products in distribution
Creating documentation of clinical trials of medical devices, coordinating trials
Communication with authorities, experts, scientific institutions, foreign contractors on registration matters, new product development, etc.
Knowledge of legislation in the area of medical devices, keeping abreast of changes and their implications for ongoing projects
Preparation of texts for packaging materials and instructions for use, support in the preparation of marketing materials
Work with R&D and other departments on new product development