Oversee the planning, execution, and maintenance of clinical evaluation activities to ensure compliance with regulatory requirements and company standards
Collate and analyze clinical data from clinical trials and testing, scientific literature, and post-market experience
Create, edit, and proofread Clinical Evaluation Reports and associated documents to assess the safety and performance of a range of MED-EL products, in accordance with applicable regulations
Build up the necessary knowledge regarding MED-EL products
Collaboration with other departments within MED EL, and with external partners
Your Profile
Master’s degree or higher degree (University, FH) in Life or Natural Sciences, Healthcare or Medicine, Engineering or Technical Sciences
Proven experience in scientific writing
Experience in regulatory affairs is benefic...
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