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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:



Compendial methods used for detecting sulfur dioxide and sulfites are prone to challenges, including false positives in sulfur-rich matrices. Eurofins Food Chemistry Testing Madison, Inc. offers a solution. Click to read about the innovative LC-MS method for determining sulfur dioxide and sulfites in food products.


Innovative ideas are common. Successfully launched products are not. Bringing a food or beverage concept to market involves far more than creativity. Our roadmap outlines the seven key stages required to take a product from initial idea to successful commercial launch—along with the risks, requirements, and technical checkpoints involved at each step. Click to read our guide for food startup and growth-stage brands.


The world of wellness is experiencing a “gummification” wave, which includes using gummies to deliver APIs as a replacement for traditional forms like pills and syrups. But this matrix doesn't come without challenges. Click to read how you can ensure the effectiveness of alternative forms like gummies, chews, drink mixes, and lozenges.


Consumer demand for clean label, natural, and plant-based products continues to drive reformulation efforts across the food and beverage industry. One of the biggest shifts in recent years has been the move away from artificial colors (FD&C dyes) in favor of natural colorants derived from fruits, vegetables, plants, and minerals. This paper outlines the common challenges when removing artificial colorants, and shares best practices for creating stable, visually appealing, and cost-effective products using natural alternatives.


Contaminants like ochratoxin A in botanicals and aflatoxins in raw materials pose serious risks to product quality and consumer health. Targeted mycotoxin testing for supplements is critical to meet global compliance standards and protect your brand from costly recalls or regulatory action. Click to learn more.


Pesticide testing is a vital part of maintaining the safety, quality, and regulatory compliance of food products. For QA and food safety managers, understanding the right time to test for pesticides and how to navigate the complex regulatory landscape is crucial for keeping consumers safe and avoiding costly compliance issues. Click to read our guide on pesticide testing to learn more.


When it comes to raw material testing, choosing the right method isn't just a box to check. It's the foundation of your quality control program. So, when should monograph tests be used? And why do they matter? Read our blog to learn more.


Dietary fiber testing in supplements is a highly complex process, requiring careful selection of testing methods customized to specific fiber sources. Many companies may struggle with choosing the right dietary fiber testing methodology, often defaulting to the most convenient or cost-effective option without realizing the implications. This blog will review common types of dietary fiber sources used in supplements along with strategies to ensure accurate and timely results.


In today’s food, dietary supplement, and beverage industry, ensuring accurate sugar content in products is more important than ever. With increasing consumer awareness about nutrition and stricter regulatory requirements, companies must verify and control the levels of sugars present in their products. Sugar testing plays a vital role in maintaining product quality, meeting labeling regulations, and supporting claims such as “low sugar,” “no added sugar,” and “zero sugar.” This blog explores the different types of sugars and sweetener alternatives and considerations when submitting products for testing.


Ensuring the safety and quality of dietary supplements is a cornerstone of regulatory compliance. Among the most critical steps in this process is establishing specifications for chemical contaminants. These contaminants, which can arise from raw materials, manufacturing processes, or environmental exposure, must be controlled to meet the standards outlined in the Code of Federal Regulations (CFR). This guide is designed to assist manufacturers in establishing strong chemical contaminant specifications while ensuring regulatory compliance.


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