
Regulatory Affairs Training – Medical Writing
Posted 6 days ago

Posted 6 days ago
This is a fully remote position, open to applicants in Germany.
• Instruction in regulatory principles and the professional crafting of medical and scientific documents
• Education on the basics of medical technology and product development
• Training in Regulatory Affairs, the EU Medical Device Regulation (MDR), and associated approval processes
• Guidance on international approval protocols for the United States, Asia, and Latin America, including MDSAP
• Development of medical and regulatory documentation during a hands-on training phase
• Personalized feedback from seasoned instructors
• Training in Medical Writing, quality management, risk management, clinical evaluation, and clinical trials
• Instruction on technical documentation, project management, innovation and development processes, and Post-Market Surveillance
• Live virtual classes from Monday to Friday, running from 8:30 a.m. to 3:30 p.m. over a span of 3 weeks, or 15 days
• Preparation for entry-level and specialized positions in Regulatory Affairs, regulatory submissions management, quality management, Clinical Affairs, and Medical Writing
• A university degree in Life Sciences, Engineering, Informatics, or a related discipline, or several years of relevant professional experience
• Proficiency in German and English at the B2 level (language skills are essential)
• Must meet the formal eligibility criteria for funding through the Federal Employment Agency or Jobcenter
• Complete funding through an education voucher provided by the Federal Employment Agency or Jobcenter
• Career guidance and personalized coaching
• Practice-oriented course framework with a significant emphasis on experiential training
• Individualized support and personal mentoring
• Virtual classrooms and collaborative workspaces
• Exceptional preparation for entering the workforce
• Certificate of participation covering all course content upon successful completion
• Work samples provided upon successful completion
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