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.

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Disclaimer:

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