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Veeva Jobs in Indiana (NOW HIRING)

Coforge

DDCS Data Engineer

Indianapolis, IN · On-site

$109K - $131K/yr

Build MCP connectors and AI-powered document ingestion pipelines for SharePoint, OneDrive, Veeva, Jama, and other document sources. * Implement RAG (Retrieval-Augmented Generation) solutions using ...

System One

Document Controller - Indy

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

System One

Document Controller - Indy

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

System One

Document Controller - Indy

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

System One

Document Controller

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

CYNET SYSTEMS

Documentation Specialist

Indianapolis, IN · On-site

$34 - $39/hr

Experience with document control systems preferred (Veeva). * Familiarity with other Adobe Creative Cloud tools (i.e., Adobe Acrobat Pro, Photoshop), Canva, Microsoft PowerPoint, Google Slides.

System One

Document Controller - Indy

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

System One

Document Controller - Indy

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

System One

Document Controller - Indy

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

System One

Document Controller - Indy

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

System One

Document Controller - Indy

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

System One

Document Controller - Indy

Indianapolis, IN · On-site

$34.94 - $41.11/hr

Demonstrated hands-on experience managing controlled documents using Veeva QualityDocs (required) * Experience supporting inspections, audits, periodic reviews, and documentation gap assessments

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Veeva information

What is a Veeva?

A Veeva job typically refers to a role involving Veeva Systems' software, which is used primarily in the life sciences industry for CRM, content management, and regulatory compliance. Professionals in Veeva roles may work as administrators, developers, consultants, or business analysts, focusing on implementing, configuring, or managing Veeva applications like Veeva Vault or Veeva CRM. These roles often require expertise in cloud-based software, data management, and industry-specific regulations.

What does a Veeva specialist or consultant do?

As a Veeva Specialist or Consultant, your daily responsibilities may include configuring Veeva Vault or Veeva CRM systems, managing user access, supporting system integrations, and responding to end-user support requests. You'll work closely with business stakeholders to gather requirements, troubleshoot issues, and ensure the software aligns with regulatory requirements in the life sciences sector. Additionally, you might collaborate with project managers, IT, and compliance teams to support new releases or process improvements. This role often requires balancing technical tasks with user training and ongoing documentation.

What are the key skills and qualifications needed to thrive in a Veeva position?

To thrive in a Veeva Specialist or Consultant role, you need a strong understanding of Veeva Vault or Veeva CRM platforms, combined with expertise in life sciences business processes and data management. Familiarity with software configuration, data migration, and certifications like Veeva Vault Administrator or Veeva CRM certification are often required. Excellent problem-solving abilities, communication skills, and the capacity to collaborate effectively with cross-functional teams distinguish top performers in this position. These competencies are critical for supporting efficient system implementations, ensuring compliance, and driving user adoption in regulated industries.

Does Veeva offer remote work options?

Veeva offers remote work options for many of its roles, including positions in software development, sales, and customer support. The availability of remote work can vary by position and location, and employees often use collaboration tools like Veeva Vault and Salesforce to work remotely effectively.

Is Veeva a good place to work?

Veeva is a technology company known for its cloud-based solutions for the life sciences industry. Employees often cite a collaborative work environment, opportunities for professional growth, and a focus on innovation, though experiences can vary by role and location.

What does Veeva actually do?

Veeva is a company that provides cloud-based software solutions primarily for the life sciences industry, including pharmaceutical and biotech companies. Jobs related to Veeva often involve developing, implementing, or supporting these software platforms, which include tools for customer relationship management (CRM), content management, and data management. Roles may require knowledge of cloud computing, industry regulations, and technical skills such as software development or system administration.

What are the most commonly searched types of Veeva jobs in Indiana?

The most popular types of Veeva jobs in Indiana are:

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For Veeva jobs in Indiana, the most frequently searched job titles are:

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Veeva jobs near you
Infographic showing various Veeva job openings in Indiana as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution.

Principal Scientist Deviation Management Lilly Medicine Foundry

Scorpion Therapeutics

Indianapolis, IN • On-site

$140 - $190/hr

Other

Posted 6 days ago

Job description

The Principal Scientist - Deviation Management leads deviation and out-of-specification (OOS) investigations, root cause analysis, CAPA development, and change control for Analytical GMP Laboratories (AGL) at the Lilly Medicine Foundry.Key Responsibilities
  • Lead Minor/Major/Critical deviation and OOS investigations using structured root cause analysis (5-Why, fishbone/Ishikawa, fault tree, Is/Is-Not).
  • Author and review deviation reports, investigation protocols, and CAPA plans meeting data integrity (ALCOA+) standards and regulatory expectations.
  • Draft risk-appropriate, measurable CAPA plans linked to verified root causes; author change control records assessing impact to validated processes, equipment, and systems.
  • Perform hands-on troubleshooting/confirmatory testing; partner with QA/SMEs/stakeholders from assignment through closure; may lead Deviation Review Board meetings.
  • Serve as an ACE team thought leader; support audit/inspection readiness via clear deviation and CAPA rationale.
  • Drive improvements using deviation metrics; track investigations/CAPAs/change controls to closure and elevate at-risk items.
  • Mentor junior investigators/analytical staff on RCA, technical writing, and quality impact evaluation.
  • Collaborate cross-functionally (Manufacturing, QA, Analytical/QC, Engineering, AGL leads) to verify corrective actions and confirm CAPA effectiveness.
Basic Qualifications
  • BS in a relevant science/technical discipline.
  • BS with 6+ years or MS with 3+ years progressive GMP manufacturing/quality/lab experience, including deviation/OOS investigations, RCA, and CAPA.
  • Experience authoring investigation protocols, technical reports, and CAPA plans in a regulated environment.
  • Authorized to work in the U.S. full-time; Lilly does not sponsor visas.
Preferred/Additional Skills
  • Working knowledge of ICH/FDA (21 CFR 210/211) and cGMP/data integrity (ALCOA+) principles.
  • Experience with TrackWise/Veeva QMS and lab informatics/GMP documentation.
  • Strong technical writing and troubleshooting; experience with change controls, risk/impact assessments (e.g., FMEA), and lot association.
  • Leadership/critical thinking; experience supporting regulatory inspections/audits.
Other Information
  • Location: Lilly Technology Center (initial) and Lilly Medicine Foundry (permanent), Lebanon, IN.
  • Travel: 0-10%.
  • Shift: first shift; occasional off-shift/weekend/holiday coverage.
  • Physical: work in gowned GMP environment; stand extended periods; handle hazardous materials/solvents with PPE.
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