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Cleaning Validation Engineer

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Job Description - Cleaning Validation Engineer

Company Description

  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

 

Job Description

Job Description:

We are seeking a Cleaning Validation Engineer with hands-on experience in the startup and validation of clean utility systems such as Water Generation Systems (WFI/RO/DI), Clean Steam Systems, Process Gas/Air Systems, Distribution Systems, Storage Tanks, and CIP/COP Systems. This role involves working in a Greenfield facility with a high-paced validation environment focused on protocol development and cleaning lifecycle execution.

Responsibilities:

  • Execute end-to-end Cleaning Validation lifecycle.
  • Specification and vendor document review.
  • Field verification and commissioning.
  • Protocol development and execution.
  • Summary and final report drafting.
  • Validate clean utility systems and equipment, including.
  • IVC washers.
  • Small parts washers.
  • CIP skids.
  • Process tanks.
  • Conduct and coordinate sample testing and tech rinses.
  • Support readiness for Phase II expansion (includes additional DSM buildings.)
  • Work collaboratively in a team preparing the site for multi-product processing (cloning strategy across sites.)
  • Manage and document work in compliance with GMP and regulatory standards.
  • Use Kneat software for digital validation lifecycle management.
  • Track approximately 800 cleaning circuits for upcoming validation work.

Requirements:

  • 2–10 years of direct experience in Cleaning Validation in a GMP environment.
  • Proficient with.
  • CIP/COP system validation.
  • Validation of clean steam, WFI, and compressed gas systems.
  • Familiarity with Kneat for electronic validation documentation.
  • Strong protocol writing and documentation skills.
  • Ability to work in a fast-paced, startup/Greenfield project environment.
  • Bachelor's degree in engineering, Life Sciences, or a related field preferred.
  • Required: 4–10 years.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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