Required Skills, Experience and Education: Bachelor's degree in a life science, technical, or related field with 12+ years of experience in the biotechnology, pharmaceutical, or medical device industry, with at least 3-5 years focused on Regulatory Affairs/Operations and Veeva RIM systems (administration, configuration, and optimization). The role includes preparing the organization for future structured data submission requirements - such as Veeva Registrations, IDMP readiness, and eCTD 4.0 - and collaborating across Regulatory Affairs, Clinical Development, Quality, Information Sciences (IS), IT, and other functions to establish integrated global processes.