MMS Holdings Inc is seeking a qualified Regulatory Operations professional to join our data-focused CRO team in the United States. You will manage regulatory documents, publish submissions in eCTD format, and ensure quality control across regulatory packages for health authorities.
The role requires a college degree in science, 3+ years in regulatory affairs/publishing, and strong MS Office/Adobe Acrobat skills. ISO/GxP familiarity and coordination with CROs are preferred.
#J-18808-LjbffrRegulatory Affairs Specialist: Elevate Submissions in phoenix at Unknown Company
This position is listed as full time and onsite.