Process Validation Engineer

Karwell Technologies
  • Indianapolis, IN
  • Quick Apply
30+ days ago

Job Description

Job Description:
We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment. The ideal candidate will have experience with process validation, equipment qualification, CSV, temperature mapping, and regulatory compliance.
Responsibilities:
  • Execute process validation and equipment qualification activities (IQ, OQ, PQ, PPQ).
  • Develop, review, and maintain validation protocols and reports.
  • Support Computer Systems Validation (CSV) activities.
  • Perform temperature mapping studies and analyze validation data.
  • Utilize Kneat or similar electronic validation management systems.
  • Support commissioning, qualification, and validation (CQV) projects.
  • Investigate deviations and support CAPA and change control activities.
  • Ensure compliance with GMP, FDA, and regulatory requirements.
  • Collaborate with Engineering, Manufacturing, Quality, and Regulatory teams.

Requirements:

  • Bachelor's degree in Engineering, Science, or a related field.
  • Experience in process validation, equipment qualification, or validation engineering.
  • Knowledge of IQ/OQ/PQ and validation lifecycle activities.
  • Familiarity with CSV principles and regulatory requirements.
  • Experience with Kneat, Ellab, or similar validation tools is preferred.
  • Understanding of GMP/cGMP regulations.
  • Strong documentation, communication, and problem-solving skills.

Preferred Skills:

  • Process Validation.
  • Equipment Qualification.
  • CSV (Computer Systems Validation).
  • Temperature Mapping.
  • Kneat.
  • Ellab Systems.
  • GMP/cGMP Compliance.
  • CAPA and Change Control.

Numbers & Facts

LocationIndianapolis, IN

Skills

  • Change Controlunmatched
  • Commissioningunmatched
  • Communication Skillsunmatched
  • Computer Systemsunmatched
  • Corrective and Preventative Action (CAPA) Systemsunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Data Analysisunmatched
  • Documentationunmatched
  • Equipment Validationunmatched
  • FDA Requirementsunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Problem Solving Skillsunmatched
  • Process Engineeringunmatched
  • Process Validationunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Regulatory Requirementsunmatched
  • System Validationunmatched
  • Temperature Mappingunmatched
  • Validation Planunmatched

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