Global Regulatory Submissions Specialist
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Job Description & How to Apply Below
MMS Holdings Inc. in Chicago seeks a Regulatory Operations professional to manage document submissions and publishing in alignment with ICH eCTD standards.
You will coordinate with CROs, vendors, and health authorities to ensure timely, compliant regulatory submissions. Ideal candidates have 3+ years in Regulatory Affairs or Publishing, strong MS Office and eCTD tooling skills, and a solid understanding of 21 CFR Part 11 and FDA guidelines.
This role, Global Regulatory Submissions Specialist at MMS Holdings Inc, could be your next career step.
Learn more about the Global Regulatory Submissions Specialist role in the description above.
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This posting is for the Global Regulatory Submissions Specialist role at MMS Holdings Inc, based in Chicago, IL, United States.
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