More jobs:
Engineering Technician
Job in
Indianapolis, Hamilton County, Indiana, 46262, USA
Listed on 2026-01-10
Listing for:
Brooksource
Full Time
position Listed on 2026-01-10
Job specializations:
-
Manufacturing / Production
Validation Engineer, Systems Engineer
Job Description & How to Apply Below
Base pay range
$25.00/hr - $30.00/hr
Associate CSV / Systems SupportRole 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
- 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
- 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
Associate
Employment typeFull-time
Job functionIT Services and IT Consulting
#J-18808-LjbffrTo View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×