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

Tucson, AZ, US • Posted 2 days ago • Updated 2 days ago
Contract W2
Contract Independent
12 Months
No Travel Required
On-site
$39 - $42/hr
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Bachelor''s Degree in Engineering or related discipline
  • Validation/Qualification Experience (1–3 years)
  • Equipment Validation
  • GxP Regulations Understanding
  • IQ/OQ/PQ Protocol Authoring and Execution
  • Technical Writing
  • Validation Documentation
  • Regulated Manufacturing Environment Experience
  • Medical Device/Pharmaceutical/Biotech Manufacturing Experience (Preferred)

Summary

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

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: 10439527
  • Position Id: 9004337
  • Posted 2 days ago
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