Regulatory Submissions & eCTD Specialist

MMS Holdings Inc is seeking a regulatory operations professional to manage document control, publishing, and submission readiness. The role requires strong ICH eCTD experience, familiarity with FDA and GCP requirements, and collaboration with CROs and vendors. The candidate should have 3+ years in regulatory affairs or a related field, with proficiency in MS Office, Adobe Acrobat, and eCTD tools, to ensure timely, compliant submissions across projects.