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Hourly Pharma Validation Engineer Jobs in Indiana

CSV Engineer I

Indianapolis, IN · On-site

$68K - $88K/yr

We are looking for a CSV Computer System Validation Engineer who will support protocol execution ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

CSV Engineer I

Indianapolis, IN · On-site

$68K - $88K/yr

We are looking for a CSV Computer System Validation Engineer who will support protocol execution ... We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors.

Data Scientist

Indianapolis, IN · On-site

$110 - $170/hr

Access, prepare, and engineer features from data processed through Apache Spark and AWS data ... pharma-specific problems and translate them into data science approaches * Build and validate ETL ...

Quality Engineer

Indianapolis, IN · On-site

$68K - $88K/yr

Pharma - aseptic handling and filling of liquid and powder APIs, dispensing custom R&D isolators ... Validation documentation * Process controls * Work with technical team in the field as well as 3rd ...

CNC MFG Engineer

Warsaw, IN · On-site

$70K - $89K/yr

Job Title: Sr CNC MFG Engineer Location: Warsaw, IN JD as below * Role: Validate CNC equipment and ... equipment validation in a regulated environment (MedTech, pharma, or healthcare devices)

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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.

Computer System Validation Engineer

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Re-posted 24 days ago


Job description

Job Title: Validation Engineer

Location: Indianapolis / Bloomington, IN (100% Onsite)

Duration: Long term Contract

Interview Mode: Onsite (Local candidates preferred)

Job Summary:

We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation activities, documentation migration, and equipment qualification to ensure compliance with regulatory standards.

Key Responsibilities

  • Lead migration of legacy validation documents into the Kneat digital platform, ensuring accuracy and compliance
  • Perform equipment qualification for lab instruments (pH meters, thermal mixers, peristaltic pumps, nutating mixers, etc.)
  • Execute temperature mapping studies, including work with Ellab systems or similar equipment
  • Support Computer Systems Validation (CSV) activities and documentation
  • Assist Process Engineering teams to ensure project timelines and milestones are met
  • Ensure all validation activities comply with GMP and regulatory requirements
  • Maintain clear, accurate, and compliant documentation

Required Qualifications:

  • Bachelor’s degree in Engineering, Science, or related field
  • 6+ years of experience in Computer Systems Validation (CSV)
  • 4+ years of experience in pharmaceutical manufacturing environment
  • Hands-on experience with equipment qualification and validation
  • Strong knowledge of CSV principles and regulatory compliance
  • Experience working in onsite, fast-paced environments