About Phibro Animal Health Corporation
Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals.
Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro’s revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide.
At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be.
If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions.
The Quality Control Tech 1 is an integral part of our Quality Control team based out of our US - Omaha, NE - Vaccines site.
Hourly rate range for this position is $22.00 - $25.00
Position Details
Quality Control Tech 1 executes critical microbiological quality control testing while performing quality assurance review and disposition activities for biologics. The role operates within a USDA‑licensed autogenous vaccine facility and partners closely with Production, Commercial Operations, Shipping/Receiving, and Diagnostics to ensure compliant, timely release or appropriate nonconformance handling of autogenous and licensed products.
Key Responsibilities
- Perform microbiological purity testing (initial and retest) per standard operating procedures, aseptic technique, and media controls; initiate and update non-conformance reports, coordinate retests, and communicate contaminant identification outcomes.
- Environmental monitoring: schedule/execute air plates by room, manage staggered testing across days, and annotate monitoring details on applicable forms.
- Media traceability & documentation: track media types/lots and associated purity tech/subculture tech records; maintain investigation files in Quality Control internal.
Key Competencies
CollaborativeCommunicating EffectivelyDelivering High Quality WorkDemonstrating InitiativeFollowing Policies and ProceduresManaging TimePrioritizing and Organizing Work
Skills
Able to develop and maintain detailed records.Extremely high level of attention to detail and high standard of quality.Must be accurate, detail-oriented and thorough.Proven ability to work effectively in a team environment.High degree of time management skills and ability to handle multiple priorities and projects at once.Must be proficient using Email, phones, cell phones, and office equipment.
Education & Experience
- Education:
- Bachelors in microbiology, Biology, Chemistry, or related field; or Associate’s with 1–3 years of relevant lab/Quality Assurance experience.
- Experience:
- 1–3+ years in Quality Control microbiology or Quality Assurance in biologics/pharma, vaccines, or regulated manufacturing.
- Demonstrated experience with non-conformance reports, deviations, and retest workflows, familiarity with certificate of analysis issuance, product disposition, and testing procedures.
- Technical Skills:
- Aseptic technique; environmental monitoring; purity testing and subculture; data review and documentation control.
- Experience with enterprise resource planning (ERP) and quality management system (QMS) platforms.
- Soft Skills:
- Strong attention to detail, root cause analysis, critical thinking and problem solving, clear written/verbal communication, and cross‑functional collaboration under time constraints.
Preferred/Helpful
- Familiarity with USDA CVB processes and regulatory requirements applicable to autogenous vaccine production.
- Familiarity with corrective and preventative action, and effectiveness check processes.
Working Conditions & Physical Requirements
- Laboratory environment with required personal protective equipment; extended periods of standing and bench work; occasional lifting of up to ~25 lbs.; Ability to work across controlled areas and coolers/incubators.
- Occasional off‑shift or weekend support to meet testing windows, monitoring schedules, or disposition timelines.
Physical Requirements
Required to lift or carry 21 to 50 lbsRequired to bend constantlyRequired to stand constantlyRequired to talk or hear constantlySpecific vision abilities include ability to adjust focusSpecific vision abilities include close visionSpecific vision abilities include distance visionSpecific vision abilities include depth perceptionSpecific vision abilities include perpheral vision
To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits
Phibro is an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law.
Business Unit: Animal Health & Mineral Nutrition
Division: Animal Health & Nutrition
Department: Quality Control
Location: US - Omaha, NE - Vaccines
Work Schedule: Monday - Friday (Standard Work hours)
