Regulatory Submissions & eCTD Specialist
Listed on 2026-10-30
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Quality Assurance - QA/QC
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Healthcare
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.
As a Regulatory Submissions & eCTD Specialist, you will play an important part at MMS Holdings Inc in Jersey City, NJ, United States.
Step into the Regulatory Submissions & eCTD Specialist role at MMS Holdings Inc in Jersey City, NJ, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
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