Junior Regulatory Consultant

Providing hands-on regulatory support, the contracted entry-level Junior Regulatory Consultant will manage document maintenance, standards management, and submission preparation activities in a remote work environment. Key Responsibilities Support ongoing standards management activities, including monitoring and maintaining applicable regulatory and consensus standards Perform routine regulatory documentation updates using established templates and procedures Assist with preparation and organization of documentation for international regulatory submissions Required Qualifications Approximately 2-5 years of experience in regulatory affairs, quality, medical device, pharmaceutical, or related industries Working knowledge of regulated documentation and document-control practices Familiarity with FDA, EU MDR/IVDR, ISO standards, and/or international regulatory frameworks Strong technical writing and research skills Ability to execute defined regulatory activities with limited strategic oversight