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.