Обязанности:
Main Responsibilities: Provides strategic planning and leadership of the Regulatory Affairs team – 8 employees (direct and matrix reporting). Ensures development and timely execution of the regulatory strategies for innovative products to support the fastest entrance to the markets across RU&CIS Cluster. Ensures development and timely execution of the regulatory strategies for legacy portfolio across RU&CIS Cluster. Provides strategic input into regulatory development programs, lifecycle management, and compliance activities. Supports cross-functional teams and projects with regulatory insights. Supports shaping of regulatory environment, advocacy and intelligence activities. Be the face of the organization to regulators, participates in appropriate forums and conveys the Company’s point of view on all relevant matters; represents the company in industrial associations if needed. Requirements: Graduate in pharmacy/ biology/ chemistry/ engineering or medicine is preferable 3 years+ experience in Regulatory Affairs for medical devices Deep and strong expertise in regulation of medical devices registration for RU&CIS countries (incl. EAEU) and international regulation Team management experience 1+ years (in direct subordination and/ or project team management, including remote teams and management of 3rd parties) Project management skills English – Upper-Intermediate+ Expertise in general business processes execution Goal oriented, responsible, dedicated Excellent communication and negotiation skills, good in listening, good problem-solving and influential skills Conditions: Competitive salary & annual bonus Medical and life insurance Meal allowance Fitness compensation Mobile allowance Opportunities for professional development and growthПохожие вакансии
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ANCOR