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Zensar Technologies

L3 - Veeva Quality Analyst

Reposted 2 Months Ago
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In-Office or Remote
Hiring Remotely in India
Senior level
In-Office or Remote
Hiring Remotely in India
Senior level
Serve as the L3 Veeva Quality subject-matter expert: own L3 escalations, triage and resolve issues, review Veeva release notes, lead integration troubleshooting across Veeva QMS/Quality Docs and connected systems (SAP, labeling), participate in technical review calls, and support post-go-live stabilization and hypercare.
The summary above was generated by AI

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)
 

Responsibilities

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
 

Qualifications

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)

About UsAt Zensar, we’re “experience-led everything”. We are committed to conceptualizing, designing, engineering, marketing, and managing digital solutions and experiences for over 130 leading enterprises. We are a company driven by a bold purpose: Together, we shape experiences for better futures. Whether for our clients, our people, or the world around us, this belief powers everything we do. At the heart of our culture is ONE with Client - a set of four core values that reflect who we are and how we work: One Zensar, Nurturing, Empowering, and Client Focus.
Part of the $4.8 billion RPG Group, we’re a community of 10,000+ innovators across 30+ global locations, including Milpitas, Seattle, Princeton, Cape Town, London, Zurich, Singapore, and Mexico City. Explore Life at Zensar and join us to Grow. Own. Achieve. Learn. to be the best version of yourself.
We believe the best work happens when individuality is celebrated, growth is encouraged, and well-being is prioritized. We are an equal employment opportunity (EEO) and affirmative action employer, committed to creating an inclusive workplace. All qualified applicants will be considered without regard to race, creed, color, ancestry, religion, sex, national origin, citizenship, age, sexual orientation, gender identity, disability, marital status, family medical leave status, or protected veteran status.

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