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John Scanga

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John Scanga, PhD

John Scanga, PhD

Chief Scientific Officer for North American Meat Division

John received his B.S. degree in Animal Sciences, his M.S. degree in Meat Science in 1997, and his Ph.D. in Animal Sciences in 1999, all from Colorado State University in Fort Collins, CO.

He developed a connection to agriculture at an early age; through work on his family’s ranching operation in central Colorado. He enrolled at Colorado State University in the fall of 1992 majoring in Animal Sciences; he competed on the CSU Meat Judging Team in 1994 and worked as an employee in the meat laboratory where his interest in meat processing and the meat industry began to grow.

Following the completion of his M.S (1997) and Ph.D. (1999), John joined the faculty at Colorado State University as an Assistant Professor and Extension Meat Specialist. He managed the day-to-day operations of the Meat Science Teaching and Research Laboratory and was promoted to Associate Professor in 2005.  He then left the university and joined IEH Laboratories and Consulting Group in January of 2008 as Vice President of Technical Services, where he continued to merge scientific concepts with industrial applications for managing and improving the safety of meat and non-meat foods, and improving food processing plant operational efficiencies.  In addition, he provided clients with regulatory, crisis event, and HACCP training and support.

John joined Elanco Animal Health in November of 2009 as an Associate Senior Technical Consultant where he brought a consumer focus and an emphasis on balancing animal productivity and performance with consumer acceptability. His work there focused on red meat safety, red meat quality and international trade.

John has been an author or co-author on over 70 refereed scientific publications on red meat quality and safety and has presented the findings of his work through numerous invited in presentations both the U.S and internationally.  

John also has a passion for service.  He currently is the chair of the Colorado Beef Council and has served as President of the Weld RE-9 school board, Weld County Fair Board and is a member of the Highland High School FFA Advisory Committee. 

John and his wife Chauna live on a diversified farming operation in Ault, Colorado.  Their family time is consumed with agriculture, farming, riding reigning horses and traveling.  His hobbies include backcountry snowmobiling and bird hunting. He  also works as a visiting professor in the Department of Animal Sciences at Colorado State University, where he first started his academic career. 

Below are resources from Dr. Scanga:



Understanding and effectively formulating lipids has become essential for today’s product developers. Whether replacing synthetic preservatives, selecting alternative oils, delivering specific health benefits, or exploring novel lipid technologies, each decision has impacts. Learn how Eurofins testing can help.


As consumer demand for women-focused health solutions accelerates, successful product development requires more than trend alignment, it demands clinically grounded, format-ready ingredient strategies. Learn more about the insights of developing functional food, beverage, and supplements products that address key women’s health needs.


Innovation in the nutraceutical and functional food space is accelerating, but commercialization is struggling to keep pace. The conversation is shifting from “What can we formulate?” to a much harder question: “What will actually work in a factory, at scale, for 12+ months?” Here are the biggest takeaways from Vitafoods Europe 2026.


Per- and polyfluoroalkyl substances (PFAS) have become a growing focus for regulators, manufacturers, and consumers alike especially when it comes to foods intended for vulnerable populations such as infants. Learn about the importance of proactive PFAS testing and how Eurofins can help here.


A dietary supplement manufacturer submitted a finished capsule product and associated raw materials for identity verification testing. The materials were labeled and supplied as Astragalus membranaceus root. Learn how our Eurofins team assisted with this request.


What makes Eurofins’ Supplement Testing Vitamin D analysis different from standard testing methods? Learn the answer to this question and more in our infographic about Vitamin D Analysis by Mass Spectrometry.


The United States Pharmacopeia (USP) is rolling out important updates to General Chapters <2021> and <2022> and, taking effect on April 1, 2026. For manufacturers who rely on microbiological testing to ensure product quality and regulatory compliance, understanding what’s changing and what actions are required is essential.


Important upcoming updates to USP Chapters <2021> and <2022 went into effect on April 1, 2026. These changes modify several microbiological testing requirements, including incubation times, suitability testing, and enrichment steps for specific organisms. Check out our answers to frequently asked questions about the updates.


With innovation comes complexity and with complexity comes risk. This is why laboratory testing isn’t just a box to check. For longevity products, it’s one of the most challenging and essential parts of responsible product development.


California’s SB 646 represents a major advancement in prenatal supplement safety. By mandating rigorous testing and transparent reporting of heavy metal levels, the state is setting a new benchmark for protecting pregnant individuals and their developing babies.


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