Descripción de la oferta
- Sin Experiencia
- Sin estudios
- Salario a negociar
Extraordinary International Consultancy
Develop successful global regulatory strategies to ensure timely device approvals: roadmaps, viability analysis, clinical evaluation, risk management.
Guide clients in decisions concerning medical device product development and promotion.
Collect and coordinate information and prepare regulatory documentation for submission to different regions worldwide (EU, USA, etc.): technical file preparation & review (CE marking), FDA clearance (510(k)) and premarket approval (PMA).
Communication with notified bodies.
Business development and marketing activities.
Establishing processes and working instructions.
Provide direct supervision of team including mentoring, training and performance management.
Sobre la empresa
Page Personnel is one of the world’s leading recruiting companies. It has been active since 1992 and, as part of PageGroup, also makes use of 40 years of experience behind Michael Page.