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Validation Engineer Equipment Validation (GxP, IQ/OQ/PQ) | Tucson, AZ | On-Site | W2 Contract

Job

Tranzeal, Inc.

Tucson, AZ (In Person)

$84,240 Salary, Full-Time

Posted 5 days ago (Updated 1 day ago) • Actively hiring

Expires 7/24/2026

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Job Description

Tranzeal is an industry leading global Business Transformation Service Provider offering specific consulting services as well as prepackaged, industry specific solutions and services to companies around the world. Our Consulting Services are dedicated to helping our clients maximize their investments in IT and the overall effectiveness and efficiency of the business. Tranzeal s deep industry experience makes us the partner of choice for a growing number of Fortune 1000 companies, midsize enterprises and small businesses worldwide. We are currently looking for ''Validation Engineer | Tucson, AZ | On-Site | W2-Contract'' to support one of our clients with the following skills:
Requirement:
Hiring Now:
Validation Engineer | Tucson, AZ | On-Site | W2 Contract We are actively seeking a Validation Engineer for a long-term contract opportunity with a leading healthcare/life sciences organization in Tucson, AZ.
Location:
Tucson, AZ Duration:
12+ Months (Possible Extension)
Pay Rate:
$39•$42/hr on W2
Work Mode:
100%
On-Site Schedule:
Monday•Friday | 8:00 AM•5:00
PM Key Responsibilities:
Execute equipment qualification and validation activities in a regulated manufacturing environment Author, review, and execute
IQ/OQ/PQ
protocols Support validation testing, documentation, and technical writing activities Validate automated and semi-automated manufacturing equipment, including filling machines, dispensers, and packaging equipment Support process validation activities as needed Ensure compliance with GxP and quality system requirements
Required Qualifications:
Bachelor''s Degree in Engineering or related discipline 1-3 years of validation/qualification experience Hands-on experience with Equipment Validation Strong understanding of GxP regulations Experience authoring and executing
IQ/OQ/PQ
protocols Technical writing and validation documentation experience Experience in medical device, pharmaceutical, or biotech manufacturing environments preferred Nice to
Have:
Experience with Cognex Vision Systems Exposure to AI-enabled camera technologies Process Validation experience
Interview Process:
Preferred Onsite Panel Interview Interested candidates can apply directly or send their updated resume to