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L3 - Veeva Quality Analyst

Open 32d posting dated 2 weeks ago
This position is no longer accepting applications(closed Aug 17, 2026).

Summary

Senior Veeva Quality Analyst leading L3 support, triaging Veeva QMS escalations, and troubleshooting integrations with SAP and other systems in a pharma environment.

A senior application expert to anchor the VEEVA Quality and hypercare function at client starting immediately. This is not a development role — it requires a technically credible professional who can lead functional discussions, triage escalations, and coordinate integrations across systems.

Key Responsibilities

• Own L3 escalations from the L1/L2 support team; triage, diagnose, and resolve
• Review Veeva release notes on a biweekly cadence and assess impact on client’s configuration
• Lead integration troubleshooting across Veeva QMS, Quality Docs, and connected systems (SAP, labeling, etc.)
• Participate in technical review calls with Veeva and internal IT teams
• Support ongoing projects stabilization post go-live

Profile Requirements

• 8–10 years of experience in Veeva quality and pharma IT applications
• Hands-on Veeva QMS experience (Quality Docs exposure a strong plus)
• Familiarity with integration patterns (APIs, middleware) — not a developer but able to lead the conversation
• Strong problem-solving and communication skills; must work independently
• Prior pharma/life sciences environment preferred (GxP awareness helpful but not mandatory for L3 role)

Key Responsibilities

• Own L3 escalations from the L1/L2 support team; triage, diagnose, and resolve
• Review Veeva release notes on a biweekly cadence and assess impact on client’s configuration
• Lead integration troubleshooting across Veeva QMS, Quality Docs, and connected systems (SAP, labeling, etc.)
• Participate in technical review calls with Veeva and internal IT teams
• Support ongoing projects stabilization post go-live

Profile Requirements

• 8–10 years of experience in Veeva quality and pharma IT applications
• Hands-on Veeva QMS experience (Quality Docs exposure a strong plus)
• Familiarity with integration patterns (APIs, middleware) — not a developer but able to lead the conversation
• Strong problem-solving and communication skills; must work independently
• Prior pharma/life sciences environment preferred (GxP awareness helpful but not mandatory for L3 role)

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