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Hourly Pharma Validation Engineer Jobs in Indiana

Hourly Production

Bluffton, IN · On-site

$15.75 - $19.50/hr

Valid Driver's License * Ability to work any shift * Ability to read and follow procedural ... Inteva has global resources for design, engineering, manufacturing and customer service for ...

Strong hands-on engineering proficiency with enterprise data science environments (such as Dataiku ... Experience working within a highly regulated manufacturing environment (such as Pharma, Diagnostics ...

Validate that Preventative maintenance functions have been completed timely and correctly. Coach ... Reviews hourly employee work logs/sheets and verifies tasks performed #lbmaintenance Requirements:

Validate that Preventative maintenance functions have been completed timely and correctly. Coach ... Reviews hourly employee work logs/sheets and verifies tasks performed #lbmaintenance Requirements:

Our focus is cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and ... cGMP pharma/biotech setting Solid foundation in the fundamentals of biochemical engineering ...

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Infographic showing various Hourly Pharma Validation Engineer job openings in Indiana as of June 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution.

OT Automation Engineer

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Posted 22 days ago


Job description

Position: OT Automation Engineer
Location: Indiana
Duration: Long Term

Job Overview

We are seeking an experienced OT Automation Engineer to support automation, controls, and manufacturing technology projects in a regulated medical device environment. The role involves working with PLCs, HMIs, automation systems, equipment validation, and system upgrades while collaborating with cross-functional teams to ensure reliable and compliant operations.

Key Responsibilities

  • Assess PLCs, HMIs, and automation-controlled manufacturing equipment.
  • Support automation system upgrades, deployments, and remediation activities.
  • Review automation documentation and identify technical or documentation gaps.
  • Coordinate testing, validation, and qualification activities (UAT, IQ, OQ, PQ).
  • Work closely with Engineering, Quality, Operations, IT/OT, and equipment vendors.
  • Document project activities and ensure automation systems remain compliant.

Required Qualifications

  • 5–10 years of experience in Automation, Controls, or OT Engineering.
  • Hands-on experience with PLCs, HMIs, and industrial automation systems.
  • Experience working in a regulated manufacturing environment.
  • Medical device, pharmaceutical, or biotechnology industry experience preferred.
  • Knowledge of automation testing, validation, and commissioning activities.
  • Experience supporting automation upgrades, migrations, or implementation projects.
  • Strong troubleshooting, documentation, and communication skills.
  • Bachelor's degree in Electrical, Controls, Automation, Computer Engineering, Mechatronics, or a related field is preferred.