Instrument Software Validation Analyst

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Title: Instrument Software Validation Analyst

Location: Cincinnati, OH (Onsite)

Type: Contract

Overview

We are seeking an experienced Instrument Software Validation Analyst to ensure that laboratory, manufacturing, and embedded software systems operate reliably, compliantly, and in accordance with regulatory requirements (GxP/FDA/EMA). The role focuses on maintaining validated systems through structured validation processes (IQ/OQ/PQ) and serves as a bridge between technical software testing and regulatory compliance.

Key Responsibilities

Software Validation & Compliance

• Validate software installed on laboratory and manufacturing instruments in compliance with EMA, FDA, and GxP guidelines
• Develop and execute validation protocols including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ)
• Ensure systems remain in a validated state throughout their lifecycle
  
  

Documentation & Regulatory Support

• Author and maintain validation documentation including:
• Validation Plans and Reports
• User Requirement Specifications (URS)
• Functional/Design Specifications
• Traceability Matrices
• Ensure compliance with 21 CFR Part 11, GAMP 5, and data integrity standards
  
  

System Analysis & Design

• Gather and document system requirements
• Develop software specifications and validation test cases
• Create infrastructure diagrams and data flow documentation
• Document current-state software configurations
  
  

Testing & Execution

• Perform functional, integration, regression, and data integrity testing
• Identify, document, and troubleshoot validation deviations
• Conduct root cause analysis and collaborate with cross-functional teams to resolve issues
  
  

Risk & Change Management

• Conduct risk assessments (e.g., FMEA) to identify and mitigate system risks
• Support and implement change control procedures for software updates and enhancements
• Transition legacy SOPs to updated IT software management SOPs
  
  

Required Qualifications

• Education: Bachelor’s degree in Computer Science, Engineering, Life Sciences, or related field
• Experience: 2–5 years of experience in Computer System Validation (CSV) or software validation in regulated industries (pharmaceutical, biotech, or medical devices)
  
  

Required Skills & Competencies

Regulatory Knowledge

• 5 years of strong understanding of:
• FDA, EMA, and GMP regulations
• 21 CFR Part 11
• GAMP 5 guidelines
• Data integrity principles
  

Technical Expertise

• 3 to 5 years of experience with:
• Laboratory systems such as LIMS
• Chromatography Data Systems (e.g., Empower)
• Familiarity with validation lifecycle and documentation standards
  
  

Core Competencies

• Strong analytical and problem-solving skills
• Excellent technical writing and documentation abilities
• Attention to detail with a quality-focused mindset
• Ability to work cross-functionally with IT, QA, and business teams
  
  

Preferred Qualifications

• Experience in global regulatory environments
• Exposure to instrument software in laboratory or manufacturing settings
• Knowledge of SOP migration and system lifecycle management