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Validation Engineer

  • Validation Engineer job type Posted on: Nov 04, 2026
  • Validation Engineer experience level BCforward
  • Validation Engineer employment type Indianapolis, Indiana
  • Validation Engineer employment type Onsite
  • Validation Engineer salary Full-time

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Job Title :

Validation Engineer

Job Type :

Full-Time

Job Location :

Indianapolis Indiana United States

Remote :

No

Jobcon Logo Job Description :

BCforward is seeking an experienced Validation Engineer to work hybrid in IndianapolisValidation Engineer – GxPLocation: Indianapolis, IN – Downtown Work Arrangement: Hybrid – Minimum 3 days onsite per weekPosition SummaryThis role focuses on application lifecycle management (ALM), validation readiness, change control, technical documentation, and release coordination for ongoing system enhancements.The ideal candidate brings strong ALM expertise, pharmaceutical validation experience, excellent documentation skills, and the ability to proactively identify gaps, coordinate remediation, and support compliant, timely application releases.Key ResponsibilitiesALM & Requirements Traceability: Review requirements, test plans, test scripts, and Requirements Traceability Matrices (RTMs). Identify gaps in requirements coverage, testing, and validation documentation.GxP Validation: Support computerized system validation (CSV), risk-based testing, and validation readiness in accordance with GxP/GMP requirements.Change Control: Prepare and review ServiceNow change requests, ensuring completeness and readiness for Pre-CRB, CRB, and subsequent approval milestones.Release Readiness: Collaborate with Product Managers, Scrum Masters, testing teams, and Quality Assurance to coordinate deliverables, resolve dependencies, and support release approvals.Continuous Improvement: Identify opportunities to improve validation, documentation, and change management processes through AI, automation, and operational efficiencies.Required QualificationsStrong knowledge of Application Lifecycle Management (ALM), including requirements management, requirements-to-test traceability, test coverage analysis, and validation documentation.Experience with GxP/GMP computerized system validation (CSV) in pharmaceutical, biotechnology, or regulated life sciences environments.Experience with regulated change control processes, validation readiness, and formal approval workflows.Strong analytical, technical documentation, and cross-functional communication skills.Ability to work independently, proactively identify issues, and coordinate resolution across multiple stakeholders.Preferred QualificationsExperience with Veeva Vault Quality/QMS, Veeva QualityDocs, or similar regulated enterprise applications.Familiarity with ServiceNow change management.Experience with Jira, Agile/Scrum, and enterprise application release processes.Familiarity with Lucid, AI-assisted documentation tools, and workflow automation.Success CriteriaThe successful candidate will ensure change requests, validation documentation, and technical deliverables are complete, accurate, and prepared for required approval milestones while proactively identifying risks and opportunities for continuous improvement.Role Focus: Validation review, ALM traceability, change control preparation, and release readiness coordination rather than primary test script execution or formal quality approval.

Jobcon Logo Position Details

Posted:

Nov 04, 2026

Reference Number:

10440_4487045616

Employment:

Full-time

City:

Indianapolis

Job Origin:

APPCAST_CPC

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BCforward is seeking an experienced Validation Engineer to work hybrid in IndianapolisValidation Engineer – GxPLocation: Indianapolis, IN – Downtown Work Arrangement: Hybrid – Minimum 3 days onsite per weekPosition SummaryThis role focuses on application lifecycle management (ALM), validation readiness, change control, technical documentation, and release coordination for ongoing system enhancements.The ideal candidate brings strong ALM expertise, pharmaceutical validation experience, excellent documentation skills, and the ability to proactively identify gaps, coordinate remediation, and support compliant, timely application releases.Key ResponsibilitiesALM & Requirements Traceability: Review requirements, test plans, test scripts, and Requirements Traceability Matrices (RTMs). Identify gaps in requirements coverage, testing, and validation documentation.GxP Validation: Support computerized system validation (CSV), risk-based testing, and validation readiness in accordance with GxP/GMP requirements.Change Control: Prepare and review ServiceNow change requests, ensuring completeness and readiness for Pre-CRB, CRB, and subsequent approval milestones.Release Readiness: Collaborate with Product Managers, Scrum Masters, testing teams, and Quality Assurance to coordinate deliverables, resolve dependencies, and support release approvals.Continuous Improvement: Identify opportunities to improve validation, documentation, and change management processes through AI, automation, and operational efficiencies.Required QualificationsStrong knowledge of Application Lifecycle Management (ALM), including requirements management, requirements-to-test traceability, test coverage analysis, and validation documentation.Experience with GxP/GMP computerized system validation (CSV) in pharmaceutical, biotechnology, or regulated life sciences environments.Experience with regulated change control processes, validation readiness, and formal approval workflows.Strong analytical, technical documentation, and cross-functional communication skills.Ability to work independently, proactively identify issues, and coordinate resolution across multiple stakeholders.Preferred QualificationsExperience with Veeva Vault Quality/QMS, Veeva QualityDocs, or similar regulated enterprise applications.Familiarity with ServiceNow change management.Experience with Jira, Agile/Scrum, and enterprise application release processes.Familiarity with Lucid, AI-assisted documentation tools, and workflow automation.Success CriteriaThe successful candidate will ensure change requests, validation documentation, and technical deliverables are complete, accurate, and prepared for required approval milestones while proactively identifying risks and opportunities for continuous improvement.Role Focus: Validation review, ALM traceability, change control preparation, and release readiness coordination rather than primary test script execution or formal quality approval.

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