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Director Validation Jobs in Arizona (NOW HIRING)

RD Partners

Validation Engineer

Tucson, AZ · On-site

$39 - $42/hr

R&D Partners is seeking to hire a Validation Engineer in Tucson, AZ . Your main responsibilities as ... Our team offers well over 200 years of combined staffing experience providing consulting, direct ...

Caterpillar

Senior Engineer-Validation

Tucson, AZ · On-site

... direct activities to mitigate risk. * Share best practices with the design teams, using tools such as Machine Readiness Summary (MRS) and presentations from the best practitioners. * As validation ...

Kelly Services

L4 Validation Technician

Chandler, AZ

$29/hr

L4 Validation Technician Chandler, Arizona Onsite: Mon - Fri 8am - 5pm Hourly Pay Rate: $29.00/hr ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

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CREXENDO, INC

Software Validation Engineer

Tempe, AZ · On-site

... direct channels. Our solutions currently support over 2.5 million end users globally and was ... Crexendo Software Validation Engineer You will be part of a team working on Crexendo's (NASDAQ:

Caterpillar Brazil

Senior Engineer-Validation

Tucson, AZ · On-site

$113 - $169/hr

... direct activities to mitigate risk.* Share best practices with the design teams, using tools such as Machine Readiness Summary (MRS) and presentations from the best practitioners.* As validation ...

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Director Validation information

See Arizona salary details

$27.7K

$131.2K

$193.2K

How much do director validation jobs pay per year?

As of Aug 21, 2026, the average yearly pay for director validation in Arizona is $131,225.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,010.00 and $181,068.00 per year, depending on experience, location, and employer.

What does a director validation do?

A Director of Validation oversees the validation processes in industries like pharmaceuticals, biotechnology, or medical devices to ensure compliance with regulatory standards. They develop and implement validation strategies for equipment, processes, and systems, ensuring they meet quality and safety requirements. This role involves managing validation teams, coordinating with regulatory bodies, and maintaining documentation to support audits and inspections. The Director also ensures adherence to industry guidelines such as FDA, EMA, or ISO standards.

What are the typical daily responsibilities of a director validation in a regulated industry?

A Director Validation typically oversees the planning, execution, and review of validation projects to ensure compliance with regulatory requirements. Daily responsibilities include leading teams, reviewing validation protocols and reports, coordinating with quality, engineering, and regulatory departments, and addressing any deviations or issues that arise during validation activities. The role may also involve direct communication with regulatory agencies during audits and inspections. This ensures products or processes meet the highest standards of quality and regulatory compliance, ultimately supporting the company’s overall operational success.

What are the key skills and qualifications needed to thrive in the director validation position, and why are they important?

To thrive as a Director Validation, you need extensive experience in validation processes, regulatory compliance, quality assurance, and a relevant scientific or engineering degree. Familiarity with industry standards, validation lifecycle management software, and certifications such as Six Sigma or PMP are highly valued. Strong leadership, strategic thinking, and excellent communication skills help to drive complex projects and foster cross-functional collaboration. These skills are vital to ensuring validated processes meet regulatory standards and support organizational goals efficiently.

What are the most commonly searched types of Validation jobs in Arizona?

The most popular types of Validation jobs in Arizona are:

What are popular job titles related to Director Validation jobs in Arizona?

For Director Validation jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Director Validation jobs in Arizona look for?

The top searched job categories for Director Validation jobs in Arizona are:

What cities in Arizona are hiring for Director Validation jobs?

Cities in Arizona with the most Director Validation job openings:

Director Validation jobs near you
Infographic showing various Director Validation job openings in Arizona as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $131,225 per year, or $63.1 per hour.

Validation Engineer

Katalyst Healthcares and Lifesciences

Tucson, AZ • On-site

Other

This job post has expired today. Applications are no longer accepted.

Job description

Job Description:
  • Client is looking for onsite Validation Engineers / CQV Engineers to support upcoming qualification work tied to sterile manufacturing and fill/finish operations. The consultants will support hands-on OQ/PQ execution, GMP documentation, protocol execution, discrepancy/deviation support, and equipment qualification activities.
  • The ideal candidate will have direct validation engineering or CQV experience in a fast-paced GMP environment, with strong exposure to fill line qualification, aseptic filling, sterile manufacturing equipment, and execution-heavy validation work. Equipment experience with autoclaves, formulation equipment, fill suites, high-velocity fillers, isolators, parts washers, tanks, and aseptic process systems is highly relevant.
  • Experience with vision systems or automated inspection systems is a strong plus, especially for candidates who have worked around high-speed fill lines or aseptic manufacturing lines. Candidates should be able to work independently onsite, execute protocols accurately, document in real time, identify discrepancies, and help drive qualification deliverables through completion.
Requirements:
  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline preferred. Equivalent hands-on validation/CQV experience in GMP manufacturing environments can be considered.
Strong Plus Skills:
  • septic Fill/Finish Equipment Experience: Exposure to isolators, high-velocity fillers, formulation equipment, fill suites, parts washers, tanks, and autoclaves.
  • Sterilization / Sterile Manufacturing Systems: Experience with SIP, VHP, autoclaves, and sterile equipment qualification.
  • Vision / Inspection System Experience: Background with vision systems or automated inspection systems, especially tied to aseptic filling or high-speed manufacturing lines.
  • Validation Tools / Execution Support: Experience using Kaye validators, wireless probes, and supporting hands-on protocol execution.
  • Documentation & Closeout: Strong ability to document execution in real time, manage discrepancies, and support protocol package closeout.
Include Must Have:
  • Hands-on validation engineering or CQV experience.
  • Strong OQ/PQ execution and documentation background.
  • Fill/finish, aseptic filling, or fill line qualification experience.
  • Sterilization or sterile manufacturing equipment experience.
  • GMP documentation experience.
  • Protocol execution experience.
  • Deviation/discrepancy support experience.
  • bility to work independently in a fast-paced project environment.
  • Experience supporting equipment qualification in a regulated life sciences environment.

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