CSV Validation Engineer

Katalyst HealthCares and Life Sciences

Posted on: April 24, 2026

Closing: May 24, 2026

Salary: Undisclosed

Job Description

Job Summary:
  • Responsible for supporting equipment and process validation activities within a regulated environment, ensuring compliance with GMP, FDA, and Food/Consumer industry standards.
  • The role focuses on validation lifecycle execution, risk-based approaches, and cross-functional collaboration to maintain product quality and regulatory compliance.

Roles & Responsibilities:
  • Develop, execute, and report IQ/OQ/PQ protocols.
  • Perform equipment and process validation activities (e.g., mixing, packaging).
  • Conduct risk assessments and support CAPA and revalidation activities.
  • Ensure compliance with GMP, FDA, and Food/Consumer industry regulations.
  • Collaborate cross-functionally with teams and support team leadership activities.

Education & Experience:
  • Bachelor's degree in engineering, Manufacturing, Life Sciences, or related field.
  • 3-7 years of experience in a regulated quality or validation environment.
  • Strong hands-on experience with IQ/OQ/PQ and risk-based validation methodologies.
  • Solid understanding of FDA, GMP, and Food/Consumer industry regulations.
  • Familiarity with MES and ERP systems (an asset).
  • Excellent communication skills and ability to work cross-functionally.
  • Experience leading or coordinating validation teams is a plus.

Katalyst HealthCares and Life Sciences

Posted on: April 24, 2026

Closing: May 24, 2026

Salary: Undisclosed

Career Focus: Validation

This role is part of a curated selection of life science opportunities featured on Xtalks. Employers may request edits or removal here.

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