aceutical, Biotechnology, and Manufacturing IT initiatives.
The ideal candidate should have strong hands-on experience with Veeva QMS / Veeva Vault, including configuration, implementation, consulting, production support, and live project delivery. Strong knowledge of regulated pharmaceutical environments and quality management processes is essential.
The role involves supporting and improving key QMS processes such as CAPA, Change Control, Quality Risk Assessments (QARs), Investigations, and Events, while ensuring compliance with GxP, FDA, ISO, CSV, and IT quality requirements.
The candidate will collaborate with business users, Quality teams, IT stakeholders, validation teams, and global project teams to deliver reliable Veeva QMS solutions, support qualification activities, manage migrations, and drive continuous improvement initiatives.
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