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Hace 21 horas
No se requiere experiencia, jornada completa, contrato indefinido
* Bachelor's Degree in Nursing, Engineering, Pharmacy, Physical or Biological science or related field of study; MS degree preferred; * Five (5) to seven (7) years' experience in the medical industry with at least three to five years in Regulatory Affairs of Medical Devices; * Scientific formation +/-master in Regulatory Affairs or MD; * Consistent background and knowledge of MD regulations; * Proven expertise in all aspects of Regulatory Affairs, Submission Preparation, local regulatory body Device Law/Regulations, World Wide Regulatory Requirements/Procedures, Project Management, and Negotiations; * Relations established with the key interlocutors in the network of the MDs (e.g., regulatory agencies, professional organizations, etc.); * Ability to identify early the risks incurred by the company, to make the necessary warnings and propose appropriate action plans, in agreement with the Quality Assurance and Regulatory Affairs Director; * Ability to work in team and to share experiences; * Excellent communications skills, including English; * Open minded, listens to others; * Customer service focused; * Able to manage complexity and Matrix organization .