Process Validation Engineer

Karwell Technologies

  • Indianapolis, IN
  • 30+ days ago

    Highlights

    The ideal candidate will have experience with process validation, equipment qualification, CSV, temperature mapping, and regulatory compliance. We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment.

    Numbers & Facts

    LocationIndianapolis, IN

    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.

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