Validation Maintenance Technician onsite in Ft. Dodge, IA- Life Sciences

CBRE Group, Inc.; Fort Dodge (IA); Hybrid; USD 60,000 - 90,000; Full time

Job summary

CBRE Group, Inc. is seeking a Validation Maintenance Technician to support thermal mapping and validation activities for autoclaves and temperature-controlled environments in a regulated pharmaceutical setting.

The role is fully onsite in Fort Dodge, IA, with cross-functional collaboration and emphasis on documentation. The candidate will execute validation protocols, calibrate equipment, analyze thermal data, and prepare qualification reports while ensuring compliance with USDA/9CFR standards

Qualifications

• Experience applying validation methods in regulated facilities.
• Familiarity with autoclaves, cycle loading, and utilities.
• Strong documentation and CAPA experience.

Responsibilities

• Participate in weekly planning meetings.
• Evaluate autoclave systems and sanitary connections.
• Generate and modify validation protocols for autoclaves.
• Set up and execute validation tasks with instrumentation.
• Calibrate sensors and verify performance.
• Collaborate with engineers and production to design load patterns.
• Install thermocouples and indicators in loads.
• Execute thermal mapping studies and collect samples.
• Document validation activities in real time.
• Analyze data and generate qualification and summary reports.
• Investigate deviations and implement corrective actions.
• Repeat validation cycles as needed.

Skills

Mechanical expertise

Validation principles

Autoclave operation

Regulatory compliance

Job description

About the role

The Validation Maintenance Technician will support thermal mapping and validation activities for autoclaves and temperature controlled environments within a regulated pharmaceutical manufacturing environment. This role requires hands‑on technical expertise, strong documentation skills, and the ability to work independently while collaborating with cross‑functional teams. The technician will be responsible for executing validation protocols, calibrating equipment, and ensuring compliance with regulatory standards.

This is a fully onsite role Monday-Friday in Ft Dodge, IA.

What you’ll do

Participate in weekly planning meetings to review upcoming assignments.

Evaluate autoclave systems to understand operational criteria, utilities, and sanitary connections.

Generate and modify validation protocols specific to autoclave and cycle parameters.

Set up and execute validation tasks using appropriate instrumentation and software.

Calibrate sensors and verify performance using built‑in software and reference tools.

Collaborate with Process Engineers and Production personnel to design validation load patterns.

Install thermocouple wires and biological indicators (Spore Strips/Ampoules) in load configurations.

Execute thermal mapping studies and retrieve biological samples for testing.

Document all validation activities and findings in real‑time during protocol execution.

Analyze thermal mapping data and generate qualification and summary reports.

Investigate deviations, perform root cause analysis, and implement corrective actions.

Repeat validation cycles as required based on load pattern frequency and protocol scope.

What you’ll need

Proficiency in mechanical expertise.

Working knowledge of validation principles and practices in a regulated manufacturing environment.

Familiarity with autoclave operation, utilities, automation, and cycle load handling.

Understanding of USDA and 9CFR regulatory requirements.

Strong analytical and troubleshooting skills.

Experience implementing corrective and preventive actions (CAPA).

High attention to detail in documentation and execution of validation activities.

Excellent verbal and written communication skills.

Ability to work collaboratively across departments.

Ability to lift up to 40lbs.

Commitment to safety protocols and awareness of hazards (e.g., high‑pressure steam, enclosed spaces).

Preferred Qualifications

Flexibility to work irregular hours, including evenings, weekends, and holidays.

Availability for frequent travel, sometimes on short notice.

Adaptability to changing scopes of work and fluctuating activity volumes.

Additional Requirements

Completion of Health, Safety, and Environmental (HSE) training.

Basic gowning training for access to controlled production areas.

Ability to work independently after initial onboarding and training.

About CBRE:

When you join CBRE, you become part of a global leader in commercial real estate and investment services that help businesses and people thrive. We are dynamic problem solvers and forward‑thinking professionals who create significant impact! Our collaborative environment is built on our shared values — respect, integrity, service, and excellence — and we value the varied perspectives, backgrounds, and skills of our people. At CBRE, you have the opportunity to chart your own course and realize your full potential!

Disclaimer:

Applicants must be currently authorized to work in the United States without the need for visa sponsorship now or in the future.