elanco

Equipment Prep Technician (Weekend shift Friday-Monday 6AM- 4:30PM)

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At a Glance

Location
Fort Dodge, Iowa, United States
Employment
Full time
Posted
2026-07-14

Key Requirements

Required Skills

ERP

Domain Knowledge

  • Biotech
  • Education
  • Manufacturing
  • Pharmaceutical
  • Regulatory

Benefits & Perks

Health Insurance

We offer a comprehensive benefits package focusing on financial, physical

Requirements

Bachelor's degree in microbiology or related scientific field; OR associate's degree with 2 years of relevant experience; OR High School Diploma/GED with 4 years of relevant manufacturing experience.

Experience in biological, pharmaceutical, biotechnology, or regulated manufacturing environments with exposure to cGMP operations and production equipment.

Knowledge of aseptic manufacturing and biological production processes combined with strong attention to detail, documentation, and compliance with cGMP and safety requirements.

Experience operating biological manufacturing equipment such as tanks, drums, autoclaves, valves, filters

Experience working with ERP or electronic inventory management systems.

Knowledge of biological organisms and vaccine manufacturing processes.

Compensation & Benefits

We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:

Multiple relocation packages

Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)

8-week parental leave

9 Employee Resource Groups

Annual bonus offering

Responsibilities

As a Manufacturing Technician, you will be part of the Manufacturing team responsible for producing high-quality animal health vaccines in a cGMP-regulated environment.

In this role, you will be responsible for operating production equipment, supporting aseptic manufacturing processes, and ensuring safe, compliant, and efficient vaccine production while driving continuous improvement initiatives.

Lead troubleshooting of complex process and equipment issues while driving process improvements to enhance efficiency, compliance, and safety

Support cGMP compliance by reviewing batch records, participating in deviation investigations, and implementing CAPAs

Monitor and analyze real-time process data to ensure operations remain within validated parameters and inform decision-making