Validation Engineer jobs in United States
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Radiant Systems Inc · 14 hours ago

Validation Engineer

Radiant Systems Inc is hiring a Validation Engineer for a major pharmaceutical client. The role involves ensuring compliance with validation standards, reviewing system configurations, and collaborating with cross-functional teams to maintain inspection readiness.

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H1B Sponsor Likelynote
Hiring Manager
Vishnu Das Natesan
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Responsibilities

Review and approve CSV lifecycle documents (VMP, URS, FRS, HDS, Risk Assessments, IQ/OQ/PQ, RTM, Summary Reports)
Ensure risk-based validation approaches aligned with GAMP 5, 21 CFR Part 11, and Data Integrity (ALCOA+) principles
Evaluate system changes through change control, assessing GxP impact and validation requirements
Support periodic reviews and re-validation activities for existing systems
Act as Quality reviewer/approver for systems including:
MES / EBR platforms (e.g., Werum PAS-X or similar)
Historians (OSIsoft PI or equivalent)
Advanced analytics tools (Seeq, used for GxP trending)
Empower and other lab systems
Review configurations related to data acquisition, time stamping, audit trails, access control, and electronic records/signatures
Ensure proper segregation between GxP vs non-GxP analytics use cases
Assess and approve data flows, interfaces, and integrations between systems
Support regulatory inspections (FDA, EMA) and internal audits related to computerized systems
Partner with Engineering, Automation, MS&T, IT, and Operations to:
Enable faster project execution with compliant validation strategies
Avoid over-validation while maintaining inspection readiness
Provide Quality input during project design, FAT/SAT, and commissioning phases

Qualification

CSV lifecycle & GAMP 521 CFR Part 11Data Integrity (ALCOA+)MES / EBR systemsProcess Historians (PI)Advanced analytics platformsRisk-based decision makingTechnical writing skillsCross-Functional Collaboration

Required

Master's degree in Engineering, Computer Science, Life Sciences, or related field
3+ years' experience in pharmaceutical or regulated manufacturing; out of which 2 years in quality organization
3+ years hands-on CSV experience reviewing and approving validation documentation
Direct experience supporting manufacturing or utilities systems (not just lab systems)
Strong working knowledge of CSV lifecycle & GAMP 5
Strong working knowledge of 21 CFR Part 11 / Annex 11
Strong working knowledge of Data Integrity (ALCOA+)
Practical experience with MES / EBR systems
Practical experience with Process Historians (PI, etc.)
Practical experience with Advanced analytics platforms (Seeq) in a GxP context
Ability to evaluate risk-based validation for dashboards, reports, and models
Familiarity with change control, deviations, and CAPA systems

Preferred

Experience with Werum PAS-X, Seeq, PI Vision, Power BI (for regulated trending)
Agile or lean validation approaches
Commissioning & Qualification (C&Q) integration with CSV
Prior involvement in FDA inspections related to computerized systems
Site digitalization or Industry 4.0 initiatives

Company

Radiant Systems Inc

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Radiant Systems, Inc. is a certified Minority Business Enterprise, a Global Consulting company founded in 1995.

H1B Sponsorship

Radiant Systems Inc has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2021 (3)

Funding

Current Stage
Late Stage

Leadership Team

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Rayn Kamesh
Head of Sales/Director, Strategic Partnership - MSP/VMS Accounts
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Company data provided by crunchbase