Cleaning Validation Engineer at Katalyst Healthcares Life Sciences
Holly Springs, NC 27539, USA -
Full Time


Start Date

Immediate

Expiry Date

10 Oct, 25

Salary

0.0

Posted On

10 Jul, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Validation, Life Sciences, Protocol Writing, Cleaning Validation

Industry

Information Technology/IT

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.
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
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