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BIVAP Research Assistant
Job in
Manhattan, Riley County, Kansas, 66503, USA
Listed on 2026-06-01
Listing for:
Phibro Animal Health Corporation A
Full Time
position Listed on 2026-06-01
Job specializations:
-
Research/Development
Clinical Research, Research Scientist -
Healthcare
Clinical Research
Job Description & How to Apply Below
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 BIVAP Research Assistant is an integral part of our Research and Development team based out of our US - Manhattan, KS site.
Compensation range for this position is $55,000.00 -$70,000.00
Position Summary
The Research Scientist is responsible for the development, review, and execution of formulation laboratory study protocols in accordance with established Standard Operation Procedures (SOPs), and Good Manufacturing Practices (GMPs). This position supports the planning, coordination, and conduct of formulation laboratory studies while ensuring accurate documentation, proper material handling, and adherence to quality and compliance standards. The role requires strong organizational skills, meticulous attention to detail, and the ability to effectively manage multiple studies concurrently.
Primary Responsibilities
* Develop, review, and execute formulation study protocols in accordance with applicable regulatory, quality, and laboratory standards.
* Conduct formulation laboratory studies in compliance with approved protocols, SOPs, and GMP requirements.
* Plan study activities, including staging materials, preparing study areas, and coordinating required resources.
* Perform feed manufacturing activities as required for studies, including appropriate sampling and documentation.
* Maintain accurate, timely, and complete documentation of all formulation study-related procedures.
* Ensure proper material and sample handling techniques to prevent cross-contamination and maintain sample integrity.
* Prepare laboratory and study areas prior to weighing and experimental procedures and perform appropriate cleaning and organization following study completion.
* Coordinate and manage multiple formulation studies simultaneously while maintaining compliance with study timelines and quality expectations.
* Communicate effectively and professionally with internal team members and external collaborators to support formulation study objectives.
Key Responsibilities
* Write, review, and execute study protocols in accordance with established laboratory standards and regulatory requirements while following all applicable Standard Operation Procedures (SOPs) and Good Manufacturing Practices (GMPs).
* Prepare for and execute formulation laboratory studies, ensuring proper planning, coordination, and documentation of all activities.
* Organize, prioritize, and balance multiple concurrent studies according to company objectives while maintaining quality and compliance standards.
* Conduct feed manufacturing activities, including sampling and documentation, while strictly adhering to approved protocols.
* Practice proper material and sample handling techniques to prevent cross-contamination and maintain sample integrity.
* Prepare and clean study areas prior to weighing activities, including staging materials and equipment.
* Perform post-study cleanup and ensure laboratory…
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