CQV Engineer

South Plainfield, NJ, US • Posted 15 days ago • Updated 2 hours ago

Full Time

On-site

Fitment

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Job Details

Skills

IQ
OQ
Management
Change Control
GMP
Electrical Engineering
Pharmaceutics
Manufacturing

Summary

Summary:
We're looking for an experienced CQV Engineer who enjoys owning equipment projects from concept to production in a highly regulated pharmaceutical environment.
Responsibilities:

This role is ideal for someone who is hands-on and technically strong - an engineer who can:
Evaluate vendors, review quotes, and recommend equipment.
Lead commissioning, qualification, and validation (IQ/OQ).
Develop SOPs, manage change control, and deliver equipment ready for GMP production.
You'll be working directly with manufacturing and packaging equipment, reviewing machine manuals and electrical drawings, and driving small projects end-to-end not as a traditional project manager, but as a technical CQV owner.

Education and experience:

5+ years of CQV experience.
Hands-on equipment validation background.
Experience in pharma / biotech / regulated manufacturing.

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: 194388808f4f71017bbfb95beb35a11e
Posted 15 days ago

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CQV Engineer

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Job Details

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Summary

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