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Strong employer brand and metro location but niche Veeva/QMS expertise reduces applicant density.
Requires niche Veeva/QMS and GxP validation experience, limiting transferability across industries.
Explicit 3–5 years, Veeva/QMS and GxP validation requirements enforce strict shortlisting.
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Own functional, regression, integration, and release testing for Quality Management System (QMS) processes in a regulated life sciences environment, primarily using Veeva Vault QMS or equivalent platforms.
Validate QMS workflows including deviations, CAPA, change control, audits, complaints, and quality events, ensuring defect identification, logging, retesting, and resolution coordination.
Collaborate with cross-functional teams across Agile delivery to support test planning, defect triage, release readiness, and production support within GxP-compliant frameworks.
3–5 years of hands-on testing experience with enterprise Quality Management Systems or regulated life sciences platforms.
Bachelor’s degree in Computer Science, Information Systems, Engineering, Life Sciences, Pharmacy, or related field.
Experience with functional, regression, integration, and user acceptance testing of QMS processes including deviations, CAPA, change control, audits, complaints, and quality events.
Hands-on expertise with Veeva Vault QMS or comparable QMS platforms and test management tools like ALM or Jira.
Experienced in testing QMS business processes and technical configurations, with strong ability to understand business requirements and assess testing impacts across workflows and integrations.
Proficient working in Agile delivery models in GxP-compliant regulated environments, demonstrating disciplined documentation and defect lifecycle management.
Comfortable collaborating with global, cross-functional teams and managing multiple testing priorities including sprint, release, and production support activities.