Regulatory Strategy Lead – FDA Submissions & Lifecycle
ritedoseColumbia, SC
Regulatory Strategy Lead – FDA Submissions & Lifecycle
L7
ritedoseColumbia, SCyesterday
Industries
Pharmaceutical Preparation ManufacturingBiological Product (except Diagnostic) ManufacturingResearch and Development in Biotechnology (except Nanobiotechnology)The Ritedose Corporation in Columbia, SC is seeking a Regulatory Affairs Manager to lead regulatory strategies for ANDA submissions and provide CDMO support for customer-led submissions (FDA and global). This role ensures compliance and lifecycle management in line with the Director of Regulatory Affairs.
Responsibilities include authoring and editing technical documents, serving as RA lead on teams, and publishing to FDA for lifecycle submissions while guiding junior staff and monitoring
Apply now
Level
ManagerL7
Location
Columbia, SC
Occupation
Regulatory Affairs Managers
Industry
Pharmaceutical Preparation Manufacturing
Posted
yesterday
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