Global Quality & Document Management Lead
Listed on 2026-10-02
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Otsuka Pharmaceutical Co., Ltd. in the United States seeks a Senior Manager to support the governance of GxP documents and the Quality System. You will contribute to continuous improvement, inspection readiness, and global SOP/WP management, collaborating with global/regional teams.
The role requires a quality-focused mindset, coordination across functions, and strong communication in English; experience with regulatory affairs and computer system validation is preferred.
We would love to welcome a new Global Quality & Document Management Lead to our team in United States.
The advertised compensation is 108..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Quality & Document Management Lead role in the description above.
We appreciate your interest in this position.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).