Medical Writer

Regulatory Content SpecialistThe role of the Regulatory Content Specialist is to develop and maintain high-quality, compliant regulatory documents. This includes creating, updating, and managing Clinical Evaluation Reports, Summary of Safety and Performance Reports, State of the Art Reviews, and Systematic Literature Reviews.Create and update CERs, SSCPs, SOAs, and LRRs in compliance with relevant regulations and guidelines.Participate in systematic literature reviews, including search, screening, data extraction, analysis, and synthesis.Analyze clinical, non-clinical, and regulatory data to perform risk/benefit assessments for medical devices.This position offers a unique opportunity for detail-oriented professionals to contribute to the development of critical regulatory documentation within the medical device sector.Key responsibilities include:Developing and maintaining regulatory contentCollaborating with cross-functional teams to ensure accuracy and completenessMaintaining up-to-date knowledge of regulatory requirements and guidelinesWe are seeking a highly organized and detail-focused individual to join our team as a Regulatory Content Specialist. If you have a passion for regulatory affairs and excellent writing skills, we encourage you to apply.