QMS Quality Engineer – Veeva Vault

Intellectt INC; Illinois; On-site; USD 100,000 - 140,000; Full time

Job summary

Intellectt INC seeks a hands-on QMS Quality Engineer to optimize and configure Veeva Vault Quality/QDocs in a regulated environment. This role focuses on enhancing configurations, security models, and workflows within Veeva Vault to support quality and compliance functions.

The ideal candidate has 5+ years in software engineering with SDLC, plus experience in the pharma and medical device industries, and can work independently in Indiana-based operations.

Qualifications

• 5+ years of software engineering/development and SDLC experience.
• Strong hands-on Veeva Vault Quality configuration experience.
• Experience in Pharma and Medical Device industries.
• Local to Indiana and willing to convert permanent.
• Ability to work independently.

Responsibilities

• Configure Veeva Vault Quality workflows, security models, and lifecycles.
• Automate quality workflows and build platform enhancements.
• Support integrations with SAP, MES, LES, Workday, and SuccessFactors.
• Troubleshoot, triage, and provide technical guidance.
• Support business process improvements across quality, manufacturing, laboratory, and compliance systems.

Skills

Veeva vault configuration

SDLC experience

Independent worker

Pharma industry experience

Medical device experience

Tools

Veeva Vault

SAP

MES

LES

LIMS

Workday

SuccessFactors

Job description

Job Title: QMS Quality Engineer Veeva Vault

Location: Indiana

Employment Type: W2

Duration: Long term

Job Summary

Seeking a hands-on QMS Quality Engineer to enhance and configure Veeva Vault Quality/QDocs in a regulated environment.

Key Responsibilities

• Configure Veeva Vault Quality workflows, security models, and lifecycles.
• Automate quality workflows and build platform enhancements.
• Support integrations with SAP, MES, LES, Workday, and SuccessFactors.
• Troubleshoot, triage, and provide technical guidance.
• Support business process improvements across quality, manufacturing, laboratory, and compliance systems.

Required Qualifications

• Local to Indiana and willing to convert permanent.
• Experience in both Pharma and Medical Device industries.
• Strong hands-on Veeva Vault Quality configuration experience.
• 5+ years of software engineering/development and SDLC experience.
• Ability to work independently.

Preferred Qualifications

• Veeva Vault/Quality Vault certification.
• Veeva Technical Lead, Senior Administrator, or Consultant experience.
• Veeva implementation/enhancement experience.
• Experience with SAP, MES/LES/LIMS, Workday, SuccessFactors, integrations, automation, or AI.