Regulatory Affairs Expert

Tasks*

Authorship of CERs and related documents in close alignment with the director of the respective therapy field

• Supportive function in risk management, in particular concerning medico-regulatory topics: Provide support in the development, maintenance and updating of documents related to risk management deliverables
• Participation in cross-functional teams for medical-regulatory aspects
• Authorship of assessments concerning product development issues, in analysis of clinical data and in defining the medical evidence needed for driving or improving product development processes in close collaboration with the therapy field director
• Planning and support of medico-scientific activities related to generation of clinical evidence (studies) in close alignment with the respective director and Clinical Research

Qualifications, experience, know-how and skills critical for success

• University degree in Medicine, pharmacy, natural science, medical engineering or related science
• At least 6 years of work experience, preferably in a comparable position within health care or pharmaceutic or medical technology companies or research institutions

Required professional experience (in years):

• Experience, preferably in the medical device business
• Knowledge of relevant regulations for medical devices (Medical Device Regulation, MDR)
• Competence in the direct compilation of medical and scientific documents, and in the coordination and collection of contributions from various persons/departments
• Experience in conducting systemic and process-oriented researches in medical and scientific databases
• Familiarity with relevant products and topics in the field of dialysis / nephrology

Required personal competencies:

• Analytical intellectual capacity
• Self-motivated, responsible and structured working method
• Diligence and resilience
• Interactive and interdisciplinary approach
• Team player
• Good communicator
• Flexibility
• Good conflict resolution skills
• Inter-cultural competence