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Validation Specialist

Katalyst HealthCares & Life Sciences

Job Description

Job Description

Job Summary:

  • We are seeking a hands-on Equipment Qualification & Process Validation Contractor to support the Enterprise Quality Change Management & Systems organization.
  • The contractor will be responsible for executing qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), for manufacturing equipment, processes, and materials within a regulated manufacturing environment.
  • This is an execution-focused role, with day-to-day direction from the Manager.
  • Success will be measured by the timely, accurate, and right-first-time completion of qualification deliverables.

Responsibilities:

  • Execute and close IQ/OQ/PQ protocols for manufacturing equipment and systems.
  • Author protocols, qualification reports, and GMP-compliant documentation.
  • Document deviations/discrepancies and maintain full record traceability.
  • Coordinate qualification activities with Manufacturing, Engineering, Quality, and Project teams.
  • Support change control, documentation remediation, and record management.
  • Execute qualification activities on the factory floor around production schedules.

Qualifications:

  • Bachelor's degree in a technical discipline or equivalent experience.
  • 5 years of hands-on IQ/OQ/PQ and process validation experience in GMP or regulated manufacturing.
  • Experience with protocol writing, execution, reports, deviations, and traceability.
  • Proficiency with eQMS (TrackWise or similar), document management systems, and MS Office/Excel.
  • CQE, CQA, ASQ, or similar certification preferred.

Top 3 Skills:

  • IQ/OQ/PQ & Process Validation.
  • Technical Writing & GMP Documentation.
  • Cross-Functional Coordination & Factory-Floor Execution.
Vacancy posted 4 days ago
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