CSV Engineer

Somerset, NJ, US • Posted 1 day ago • Updated 7 hours ago
Full Time
On-site
Fitment

Dice Job Match Score™

📋 Comparing job requirements...

Job Details

Skills

  • FOCUS
  • IQ
  • OQ
  • PQ
  • Enterprise Resource Planning
  • Reporting
  • Collaboration
  • Quality Assurance
  • Business Data
  • Regulatory Compliance
  • Change Control
  • Documentation
  • Risk Assessment
  • Traceability Matrix
  • Computer Science
  • Computerized System Validation
  • Pharmaceutics
  • Life Sciences
  • Test Scripts
  • Master Data Management
  • SAP
  • Data Lake
  • Interfaces
  • Snow Flake Schema
  • Artificial Intelligence
  • GxP
  • Data Integrity
  • Management

Summary

Summary:
IT CSV Validation Engineer is responsible for authoring and executing validation test scripts to support regulated systems within a GxP life sciences environment.
This role will focus on validating ERP Master Data Governance processes and Data Lake platforms, ensuring compliance with regulatory requirements and data integrity standards.

Roles & Responsibilities:
  • Author, review, and execute validation test scripts (IQ/OQ/PQ) for GxP computerized systems
  • Support validation activities for ERP Master Data Governance processes, ensuring data accuracy, integrity, and compliance
  • Perform validation of Data Lake platforms and associated system interfaces, including data ingestion, transformation, and reporting layers
  • Collaborate with cross-functional teams (IT, QA, Business, Data Engineering) to define validation scope, risk assessments, and acceptance criteria
  • Ensure compliance with GxP, 21 CFR Part 11, and data integrity requirements throughout the system lifecycle
  • Support deviation investigations, CAPAs, and change control activities related to validated systems
  • Maintain validation documentation including Validation Plans, Risk Assessments, Traceability Matrices, and Summary Reports

Education & Experience:
  • Bachelor's degree in Computer Science, Engineering, Life Sciences, or related discipline
  • 5+ years of Computer System Validation (CSV) experience in pharmaceutical or life sciences environments
  • Strong experience with test script authoring and execution for GxP systems
  • Experience supporting Master Data Governance processes (SAP experience preferred but not required)
  • Experience validating Data Lake environments and system interfaces (Snowflake experience preferred)
  • Familiarity with AI/advanced data platforms is a plus
  • Experience with validation management tools such as Val Genesis is a plus
  • Strong understanding of GxP, 21 CFR Part 11, and data integrity principles
  • Ability to work independently and manage multiple validation activities with minimal oversight
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91116760
  • Position Id: 6cd6c615f5b3abf552fbf7733bc72abc
  • Posted 1 day ago
Create job alert
Set job alertNever miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

South Plainfield, New Jersey

Today

Full-time

Branchburg, New Jersey

Today

Full-time

Raritan, New Jersey

2d ago

Easy Apply

Full-time

Raritan, New Jersey

Today

Full-time

USD 132,000.00 - 150,000.00 per year

Search all similar jobs