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Temporary Validation Engineer Jobs (NOW HIRING)

Temporary, entry-level position to mitigate expected validation workload Review requirements ... IT, Engineering, Science or equivalent experience Preferred minimum 1-2 years of relevant ...

Temporary Assignment Work Type: Onsite Shift: Monday to Friday from 08:00 AM to 05:00 PM Summary The Validation Engineer / Equipment Validation Engineer supports and executes QC laboratory equipment ...

Hardware Validation Engineer Pay rate: $40.94 - $54.15/hr. Location: Palo Alto, CA Zip Code: 94304 ... We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We ...

... test engineer/validation engineer etc. -Can understand schematics/datasheets, trouble-shoot ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

PR · On-site

Location: south-east of the island Temporary roles Qualifications * Bachelor in engineering or science and 3 years of experience as validation consultant in regulated industry. * Excellent technical ...

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Temporary Validation Engineer information

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How much do temporary validation engineer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for temporary validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What is the difference between Temporary Validation Engineer vs Validation Technician?

AspectTemporary Validation EngineerValidation Technician
CredentialsBachelor's degree in engineering, life sciences, or related field; some roles may require certifications in validation or quality assuranceAssociate's or bachelor's degree in a technical field; certifications are less common but beneficial
Work EnvironmentInvolved in validation planning, protocol development, and oversight; often collaborates with cross-functional teamsPerforms hands-on validation testing, equipment calibration, and data collection
Employer & Industry UsageUsed in pharmaceutical, biotech, and medical device industries for validation projectsCommonly employed in manufacturing and quality assurance departments within similar industries

The Temporary Validation Engineer typically oversees validation processes, requiring more advanced knowledge and planning skills, while the Validation Technician focuses on executing validation tests and data collection. Both roles are essential in ensuring compliance and quality in regulated industries, but they differ in responsibilities and required experience.

More about Temporary Validation Engineer jobs
What cities are hiring for Temporary Validation Engineer jobs? Cities with the most Temporary Validation Engineer job openings:
What are the most commonly searched types of Validation Engineer jobs? The most popular types of Validation Engineer jobs are:
What states have the most Temporary Validation Engineer jobs? States with the most job openings for Temporary Validation Engineer jobs include:
Infographic showing various Temporary Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer (temporary)

University of Colorado

Aurora, CO • On-site

$32 - $40/hr

Full-time

Posted 22 days ago


University Of Colorado Boulder rating

8.2

Company rating: 8.2 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

142nd of 617 rated colleges and universities


Job description

University of Colorado Anschutz
Department: Gates Institute Biomanufacturing Facility
Job Title: Validation Engineer (temporary)
Position#00779113 requisition# 40578
This is a temporary position limited to no more than 9-months
Job Summary:
The University of Colorado Anschutz is seeking a temporary Validation Engineer to join the Gates Institute Biomanufacturing Facility (GBF) in Aurora, CO. The GBF is an academic Phase I cGMP contract manufacturing facility dedicated to the development and manufacture of novel biologics and cell therapies for early-phase clinical trials and serves as a core capability that differentiates the University in both regenerative medicine and traditional biotechnology.
Within the dynamic environment of the Gates Institute Biomanufacturing Facility, serve as the architect of the site's equipment management program. The Validation Engineer will support the review and release of GMP equipment post calibration, oversee new equipment onboarding including Installation Qualification (IQ), Operation Qualification (OQ), and Process Qualification (PQ), optimize the eQMS equipment management system and surrounding SOPs and paper forms, and monitor metrics to ensure compliance.
Key Responsibilities:
• Support Facilities to schedule and coordinate instrument and equipment calibrations and preventative maintenance (PM) activitie
• Review and release instrument and equipment post calibration and PM activitie
• Oversee and the new equipment onboarding process including guiding IQ, OQ, and PQ studies and report
• Optimize the eQMS asset management system including updating SOPs and paper form
• Monitor asset compliance, metrics, and effectiveness of the equipment management program
Work Location:
Onsite - this role is expected to work onsite and is located in Aurora, CO.
Why Join Us:
Join the Gates Institute Biomanufacturing Facility and be part of a team turning cutting-edge science into real therapies for patients. At the GBF, your work directly supports the development and manufacture of novel biologics and cell therapies advancing into early-phase clinical trials, offering a rare opportunity to contribute to life-changing innovation at the intersection of academia and industry.
Qualifications:
Minimum Qualifications:
• Bachelor's degree in scientific discipline or related field, or an equivalent combination of education and relevant experience.
• Minimum of three (3) years of experience administering and maintaining a GMP instrument/equipment program or learning management system within a regulated life sciences environment.
Applicants must meet minimum qualifications at the time of hire.
Preferred Qualifications:
• Experience developing GMP equipment validation program.
• Knowledge of FDA cGMP regulations, FACT standards, and GMP documentation practices.
• Experience developing IQ, OQ, and PQ protocols for GMP equipment.
Knowledge, Skills and Abilities:
• Ability to communicate effectively, both in writing and orally. Strong English verbal and written communication skills required. Ability to accurately read, interpret, and produce technical documentation.
• Ability to establish and maintain effective working relationships with employees at all levels throughout the institution.
• Outstanding customer service skills.
• Highly self-motivated and organized, with the ability to work both independently and collaboratively in a fast-paced, team-oriented environment.
• Technical writing ability to draft and edit controlled documents such as SOPs, Work Instructions (WIs), and forms.
Conditions of Employment:
Strong English verbal and written communication skills required, with the ability to accurately read, interpret, and produce technical documentation.
How to Apply:
For full consideration, please submit the following document(s):
1. A letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position
2. Curriculum vitae / Resume
3. Five professional references including name, address, phone number (mobile number if appropriate), and email addre
Applications are accepted electronically ONLY at www.cu.edu/cu-careers.
Questions should be directed to: Chris Freedman, christopher.freedman@cuanschutz.edu
Screening of Applications Begins:
Immediately and continues until July 27, 2026.
Anticipated Pay Range:
Thehiring range for this position has been established at: $32.00 to $40.00 / hour.
The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. The salary of the finalist(s) selected for this role will be set based on a variety of factors, including but not limited to, internal equity, experience, education, specialty and training.
Your total compensation goes beyond the number on your paycheck. Temporary employees are only eligible for sick leave benefits.
Equal
Employment Opportunity Statement:
The University of Colorado (CU) is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing nondiscrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities.
ADA Statement:
The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at hr.adacoordinator@ucdenver.edu.
Background Check Statement:
The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees.
Vaccination Statement:
CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine preventable diseases. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety sensitive job duties, you must enroll in the occupational health medical surveillance program.

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