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Director Computer System Validation Csv Jobs in Indiana

Demonstrated experience performing computer systems validation for building management or control ... Direct experience validating Metasys BMS platform. Experience validating AVEVA PI Historian, DeltaV ...

The Associate Director of Enterprise Systems serves as the enterprise system and process owner for ... Oversee Computer System Assurance (CSA) and Computer System Validation (CSV) activities for all ...

Exposure to Computer System Validation (CSV) and Computer Software Assurance (CSA) methodologies. 📩 If you are interested in this position, please send your updated CV by email to rintisaha ...

Senior MES Engineer

Fishers, IN

$97K - $134K/yr

Provide technical support to Computer System Validation (CSV) activities, including MES qualification and data integrity assessments. Work closely with IT to implement OT solutions in an integrated ...

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Director Computer System Validation Csv information

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Computer System Validation Engineer

Stark Pharma Solutions Inc

Indianapolis, IN • On-site

Contractor

Posted 13 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