Specialist - Fill/Finish Operations - Sun - Thurs 10:00 pm - 6:30 am
Quick Summary
Manufacture and compound sterile solutions and other parenteral products, including obtaining, weighing, measuring, and adding raw materials according to production procedures. Set up, operate,
Manufacture and compound sterile solutions and other parenteral products, including obtaining, weighing, measuring, and adding raw materials according to production procedures. Set up, operate,
Requirements
~1 min read- Education: High School Diploma or GED.
- Experience: Experience working in a manufacturing, production, laboratory, or similar regulated environment preferred.
- Skills: Ability to perform calculations and conversions involving weights, volumes, and percentages; computer aptitude with the ability to learn and adapt to new platforms and software.
- Knowledge of hazardous waste handling, decontamination, sterilization, and BPE methods.
- Understanding of basic cGMP and documentation practices.
- Knowledge of basic laboratory practices, biology, and microbiology.
- Understanding of aseptic manufacturing or processing environments.
- Mechanical aptitude with an understanding of manufacturing systems, equipment, and processes.
As a Fill/Finish Operator, you will support sterile manufacturing operations by filling antigen serials and preparing final product formulations. In this role, you’ll independently perform product processing in accordance with standard operating procedures (SOPs), Manufacturing Directions, cGMP requirements, and proper aseptic techniques to ensure product quality and sterility.
Responsibilities
~1 min read- →Manufacture and compound sterile solutions and other parenteral products, including obtaining, weighing, measuring, and adding raw materials according to production procedures.
- →Set up, operate, inspect, and dismantle production equipment for cleaning while assessing equipment and materials for readiness prior to use.
- →Assemble antigens into final product formulations and prepare adjuvants and other intermediates while maintaining product sterility.
- →Accurately verify and document the identity of components used in formulation while adhering to cGMP documentation requirements.
- →Follow Standard Operating Procedures (SOPs), Filling Manufacturing Directions, and established aseptic processing practices.
- Overtime may be required based on production demands.
- Ability to lift up to 50 lbs.
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
Location & Eligibility
Listing Details
- Posted
- October 7, 2026
- First seen
- October 7, 2026
- Last seen
- October 7, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 55%
- Scored at
- October 7, 2026
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