MMS Holdings Inc. is a data-driven CRO seeking a Regulatory Operations professional to manage submission lifecycle and document control. You will publish submissions in eCTD format and ensure quality and compliance across all regulatory documents. Ideal candidates have 3+ years in regulatory affairs, strong MS Office/Adobe skills, and familiarity with eCTD tools. Join a collaborative team supporting pharma, biotech, and device clients across a global footprint.

Also on the board Same function, level within a rung

Level

Senior

Location

Chicago, IL

Occupation

Regulatory Affairs Specialists

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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