Validation Engineer

Bethel, CT, US • Posted 12 hours ago • Updated 12 hours ago

Full Time

On-site

Fitment

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Job Details

Skills

Documentation
ISO 9000
ISO 13485
Manufacturing Engineering
FOCUS
IQ
OQ
PQ
Manufacturing
Medical Devices
Drawing

Summary

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.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: f75f9b989d01996027d5450c9818cfe3
Posted 12 hours ago

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Validation Engineer

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Job Details

Skills

Summary

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