System Technician

Brooksource; Indianapolis (IN); On-site; USD 34,440 - 41,328; Full time

Job summary

A leading technology and consulting firm is seeking an Associate CSV / Systems Support professional. This position is ideal for early-career individuals seeking hands-on experience in a GMP-regulated environment. The role involves supporting validation documentation, coding and configuration work, and performing testing to ensure systems operate correctly. Candidates should hold a Bachelor's degree in a related field with a basic understanding of CSV principles. Full-time employment is offered, focusing on IT services and consulting.

Qualifications

• Bachelor’s degree in Engineering, Computer Science, Information Systems, Life Sciences, or a related field.
• Basic understanding of CSV principles and work within regulated environments.
• Familiarity with GMP concepts and documentation expectations.

Responsibilities

• Provide associate-level CSV execution support for equipment and systems.
• Assist with validation documentation activities, including protocol execution.
• Support coding and configuration work for systems following established standards.
• 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.
• Maintain accurate documentation to support inspection readiness.
• Collaborate with users, manufacturing partners, and senior technical resources.

Skills

Attention to detail

Basic understanding of CSV principles

Familiarity with GMP concepts

Exposure to coding, scripting, or system configuration

Education

Bachelor’s degree in Engineering, Computer Science, or related field

Job description

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