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Engineering Technician

Job in Indianapolis, Hamilton County, Indiana, 46262, USA
Listing for: Brooksource
Full Time position
Listed on 2026-01-10
Job specializations:
  • Manufacturing / Production
    Validation Engineer, Systems Engineer
Salary/Wage Range or Industry Benchmark: 25 - 30 USD Hourly USD 25.00 30.00 HOUR
Job Description & How to Apply Below
Location: Indianapolis

Base pay range

$25.00/hr - $30.00/hr

Associate CSV / Systems Support

Role Overview

This associate‑level position supports computer system validation (CSV) and system configuration activities
. The role focuses on execution and support for equipment and systems under the guidance of senior validation, automation, or IT resources.

The position is well‑suited for early‑career professionals seeking hands‑on experience in a GMP‑regulated setting.

Key Responsibilities
  • Provide associate‑level CSV execution support for equipment and systems
  • Assist with validation documentation activities
    , including protocol execution, test evidence collection, and traceability updates
  • Support coding and configuration work for systems following established standards, templates, and procedures
  • Perform basic functional testing and verification to confirm systems operate as intended
  • Execute work in compliance with approved SOPs, GDP, and data integrity requirements
  • Support change activities, deviation follow‑ups, and documentation revisions as assigned
  • Maintain accurate, organized documentation to support inspection readiness
  • Collaborate with users, manufacturing partners, and senior technical resources
Required Qualifications
  • Bachelor’s degree in Engineering, Computer Science, Information Systems, Life Sciences, or a related field (or equivalent experience)
  • Basic understanding of CSV principles and work within regulated environments
  • Familiarity with GMP concepts and documentation expectations
  • Exposure to coding, scripting, or system configuration activities (academic, internship, or entry‑level professional experience acceptable)
  • Strong attention to detail and ability to follow written procedures
Preferred Qualifications
  • Experience supporting systems or platforms
  • Prior experience in a pharmaceutical manufacturing environment
  • Internship or entry‑level experience in validation, QA, automation, or systems support
  • GMP‑regulated environment requiring strict adherence to procedures and documentation standards
Seniority level

Associate

Employment type

Full-time

Job function

IT Services and IT Consulting

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