Quality System Specialist (Veeva eQMS)

Role: Veeva eQMS Specialist responsible for leading or supporting Veeva Vault implementations within QualityDocs, QMS, and Training modules in a regulated biopharma environment. Objectives include optimizing the Veeva ecosystem to support compliant, efficient quality operations and process improvements. Responsibilities encompass configuring workflows, conducting process mapping, facilitating cross-functional training, managing document migrations, supporting audits, and ongoing system support. Qualifications: Bachelor’s degree or 3-5 years industry experience; minimum of 3 years QA experience in GMP settings; hands-on Veeva Vault implementation expertise; Veeva Vault Administrator or Vault Quality certification preferred. High-Value: experience with GxP, 21 CFR Part 11, Annex 11, global teams, and regulated environments; supporting continuous improvement post-implementation. Collaboration with Quality and cross-functional teams to enhance QMS processes and documentation readiness for audits and inspections. Location: Not specified; likely office-based given typical industry standards. Salary: $95,000–$115,000 annually.