Filling Operator (Mon-Fri 10:00 pm - 6:30 am)
Elanco
August 29, 2026
On-site
Fort Dodge, IA
Operations
Your Role: Fill/Finish Operator
Responsibilities:
- Fill serials of antigen using proper aseptic techniques, in accordance with standard methods, SOPs, and Manufacturing Directions.
- Manufacture and compound sterile solutions and other parenteral products, including obtaining, weighing, measuring, and adding raw materials per production procedures.
- Set up, operate, and dismantle production equipment for cleaning; perform inspections and assess equipment/material condition prior to use.
- Assemble antigens into final product formulations and prepare adjuvants/other intermediates, maintaining product sterility.
- Verify and document component identities and adhere to cGMP documentation practices.
- Comprehend and follow Standard Operating Procedures/Filling Manufacturing Directions.
Minimum Qualifications:
- High School Diploma/GED
- Ability to perform calculations and conversions involving weights, volumes, and percentages.
- Computer aptitude to adapt to future platforms and software.
Preferred Qualifications (Competitive Edge):
- Knowledge of hazardous waste handling, decontamination and sterilization, and BPE methods.
- Understanding of basic GMP/documentation practices, basic laboratory practices, biology, and microbiology.
- Understanding of operating in an aseptic environment.
- Mechanical aptitude; understanding of systems, equipment, and processes.
Additional Information:
- Overtime may be required depending on production demands.
- May require lifting up to 50 lbs.
Responsibilities:
- Fill serials of antigen using proper aseptic techniques, in accordance with standard methods, SOPs, and Manufacturing Directions.
- Manufacture and compound sterile solutions and other parenteral products, including obtaining, weighing, measuring, and adding raw materials per production procedures.
- Set up, operate, and dismantle production equipment for cleaning; perform inspections and assess equipment/material condition prior to use.
- Assemble antigens into final product formulations and prepare adjuvants/other intermediates, maintaining product sterility.
- Verify and document component identities and adhere to cGMP documentation practices.
- Comprehend and follow Standard Operating Procedures/Filling Manufacturing Directions.
Minimum Qualifications:
- High School Diploma/GED
- Ability to perform calculations and conversions involving weights, volumes, and percentages.
- Computer aptitude to adapt to future platforms and software.
Preferred Qualifications (Competitive Edge):
- Knowledge of hazardous waste handling, decontamination and sterilization, and BPE methods.
- Understanding of basic GMP/documentation practices, basic laboratory practices, biology, and microbiology.
- Understanding of operating in an aseptic environment.
- Mechanical aptitude; understanding of systems, equipment, and processes.
Additional Information:
- Overtime may be required depending on production demands.
- May require lifting up to 50 lbs.