Filling Operator (Mon-Fri 10:00 pm - 6:30 am)
Elanco
August 07, 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 equipment for cleaning; inspect and assess equipment and material condition prior to use.
- Assemble antigens into final product formulations and prepare adjuvants or 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.
What You Need to Succeed (Minimum Qualifications):
- High School Diploma/GED.
- Ability to perform calculations/conversions involving weights, volumes, and percentages.
- Computer aptitude to adapt to future platforms and software.
What Will Give You a Competitive Edge (Preferred Qualifications):
- 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 and understanding of systems, equipment, and processes.
Additional Information:
- Overtime may be required.
- 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 equipment for cleaning; inspect and assess equipment and material condition prior to use.
- Assemble antigens into final product formulations and prepare adjuvants or 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.
What You Need to Succeed (Minimum Qualifications):
- High School Diploma/GED.
- Ability to perform calculations/conversions involving weights, volumes, and percentages.
- Computer aptitude to adapt to future platforms and software.
What Will Give You a Competitive Edge (Preferred Qualifications):
- 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 and understanding of systems, equipment, and processes.
Additional Information:
- Overtime may be required.
- May require lifting up to 50 lbs.