Validation Specialist

Katalyst HealthCares and Life Sciences

$80K — $95K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Life Sciences, or related discipline.
  • 5+ years of hands-on validation experience with GMP equipment and utilities.
  • Strong understanding of cGMP, GDP, and SOP requirements for documentation.
  • Experience with temperature mapping and requalification procedures.
  • Familiarity with cleaning validation protocols.

Responsibilities

  • Support cleaning validation activities and protocol execution.
  • Perform temperature mapping and requalification of controlled temperature units.
  • Execute IQ/OQ/PQ validation and conduct periodic reviews for GMP equipment.
  • Assist with the commissioning and installation of modified equipment.
  • Generate comprehensive validation documentation per regulatory standards.
  • Support validation lifecycle activities and manage change controls.
  • Engage in audit readiness and provide regulatory inspection support.

Benefits

  • Opportunity for professional development and continuing education.
  • Collaborative work environment with a focus on teamwork.
  • Engagement in cutting-edge projects within the life sciences sector.
Full Job Description
Requirements:
  • Support cleaning validation activities, protocol execution, sampling, and documentation.
  • Perform temperature mapping and requalification of controlled temperature units.
  • Execute IQ/OQ/PQ, requalification, and periodic review for GMP equipment and utilities.
  • Support commissioning, installation, and qualification of new or modified equipment.
  • ssist with equipment troubleshooting alongside Engineering and Operations.
  • Generate validation documentation following cGMP, GDP, and SOP requirements.
  • Support validation lifecycle activities, change controls, investigations, and CAPAs.
  • Participate in audit readiness and regulatory inspection support.
  • Bachelor's degree in Engineering, Life Sciences, or related discipline required.
  • 5+ years of hands-on validation experience with GMP equipment and utilities.

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