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

CBRE; Fort Dodge (IA); On-site; USD 65,000 - 90,000; Full time

Job summary

CBRE is seeking a Validation Maintenance Technician to support thermal mapping and validation activities for autoclaves and temperature-controlled environments in a regulated pharmaceutical manufacturing setting. This onsite role in Fort Dodge, IA requires hands-on technical expertise, precise documentation, and the ability to work independently with cross-functional teams.

You will execute validation protocols, calibrate equipment, set up tests, collect samples, analyze data, and prepare

Qualifications

• Proficiency in mechanical expertise.
• Working knowledge of validation principles in regulated manufacturing.
• Familiarity with autoclave operation and cycle handling.
• Understanding USDA and 9CFR regulatory requirements.
• Strong analytical and troubleshooting skills.
• Experience implementing CAPA.
• High attention to documentation and execution of validation activities.
• Excellent verbal and written communication skills.

Responsibilities

• Review upcoming assignments in weekly planning meetings.
• 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 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.

Skills

Mechanical expertise

Validation principles

Autoclave operation

Analytical skills

Troubleshooting

CAPA experience

Documentation skills

Communication skills

Cross-functional collaboration

Job description

About The Role

The Validation Maintenance Technician willsupport thermal mapping and validation activities for autoclaves andtemperature controlled environments within a regulated pharmaceuticalmanufacturing environment. This role requires hands-on technical expertise,strong documentation skills, and the ability to work independently whilecollaborating with cross-functional teams. The technician will be responsiblefor executing validation protocols, calibrating equipment, and ensuringcompliance with regulatory standards. This is a fully onsite role Monday-Friday in FtDodge, IA.

What You’ll Do

• Participate in weekly planning meetings toreview upcoming assignments.
• Evaluate autoclave systems to understandoperational criteria, utilities, and sanitary connections.
• Generate and modify validation protocolsspecific to autoclave and cycle parameters.
• Set up and execute validation tasks usingappropriate instrumentation and software.
• Calibrate sensors and verify performance using built-insoftware and reference tools.
• Collaborate with Process Engineers andProduction personnel to design validation load patterns.
• Install thermocouple wires and biologicalindicators (Spore Strips/Ampoules) in load configurations.
• Execute thermal mapping studies and retrievebiological samples for testing.
• Document all validation activities and findingsin real-time during protocol execution.
• Analyze thermal mapping data and generatequalification and summary reports.
• Investigate deviations, perform root causeanalysis, and implement corrective actions.
• Repeat validation cycles as required based onload pattern frequency and protocol scope.

What You’ll Need

• Proficiency in mechanical expertise.
• Working knowledge of validation principles andpractices in a regulated manufacturing environment.
• Familiarity with autoclave operation,utilities, automation, and cycle load handling.
• Understanding of USDA and 9CFR regulatoryrequirements.
• Strong analytical and troubleshooting skills.
• Experience implementing corrective andpreventive actions (CAPA).
• High attention to detail in documentation andexecution of validation activities.
• Excellent verbal and written communicationskills.
• Ability to work collaboratively acrossdepartments.
• Ability to lift up to 40lbs.
• Commitment to safety protocols and awareness ofhazards (e.g., high-pressure steam, enclosed spaces).

Preferred Qualifications

• Flexibility to work irregular hours, includingevenings, weekends, and holidays.
• Availability for frequent travel, sometimes on shortnotice.
• Adaptability to changing scopes of work andfluctuating activity volumes.

Additional Requirements

• Completion of Health, Safety, and Environmental(HSE) training.
• Basic gowning training for access to controlledproduction areas.
• Ability to work independently after initialonboarding and training.

AboutCBRE

Whenyou join CBRE, you become part of a global leader in commercial real estate andinvestment services that help businesses and people thrive. We are dynamicproblem solvers and forward-thinking professionals who create significantimpact! 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 tochart your own course and realize your full potential!

Disclaimer

Applicantsmust be currently authorized to work in the United States without the need forvisa sponsorship now or in the future.

Equal Employment Opportunity: CBRE is an equal opportunity employer that values diversity. We have a long-standing commitment to providing equal employment opportunity to all qualified applicants regardless of race, color, religion, national origin, sex, sexual orientation, gender identity, pregnancy, age, citizenship, marital status, disability, veteran status, political belief, or any other basis protected by applicable law.

Candidate Accommodations: CBRE values the differences of all current and prospective employees and recognizes how every employee contributes to our company’s success. CBRE provides reasonable accommodations in job application procedures for individuals with disabilities. If you require assistance due to a disability in the application or recruitment process, please submit a request via email at [e-mail] or via telephone at [phone] (U.S.) and [phone] (Canada).