Validation Engineer

Katalyst Healthcares & Life Sciences • Bethel, Connecticut, United States • Posted May 16, 2026

Location Bethel, Connecticut
Job Type Full-time
Category other-general
Posted May 16, 2026
Summary:

This is a hands-on, onsite role focused on equipment installation, IQ/OQ execution, and validation documentation within a regulated manufacturing environment (ISO 9001 / ISO 13485). The team is looking for someone who can support qualification activities as the equipment comes online. The role works directly with the Manufacturing Engineering Manager and is execution-focused — ideal for someone who enjoys being on the floor, owning validation deliverables, and supporting equipment readiness in a fast-paced environment.

Required skills:

  • Strong focus on IQ and OQ (no PQ ownership).

  • Regulated manufacturing experience required (medical device strongly preferred).

  • Exposure to tube drawing, metal processing, or Nitinol is a plus, but not required.



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