Global Quality Documentation Lead
Job in
Augusta, Kennebec County, Maine, 04338, USA
Listed on 2026-07-14
Listing for:
Otsuka America Pharmaceutical Inc.
Full Time
position Listed on 2026-07-14
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Job Description & How to Apply Below
Otsuka America Pharmaceutical Inc. is seeking a qualified professional to manage global, regional and local quality documents and related activities.
You will contribute to continuous improvement of the Otsuka Quality System, inspection management, regulatory intelligence, validation activities and project liaison tasks as needed. The role requires advanced knowledge of regulatory requirements across Pharmacovigilance, Clinical Development and related areas, with a focus on GxP and QA.
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