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Andrzej Benkowski

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Andrzej Benkowski

Andrzej Benkowski

Technical Manager, Probiotics & Dietary Supplements

As the Technical Manager at Eurofins Center of Excellence for Probiotics, Andrzej Benkowski brings over 18 years of expertise in biotics quality management, testing, and technology. With a strong technical background in food microbiology, Andrzej specializes in contract R&D, method development, and pioneering technologies for probiotic evaluation.

Since 2019, Andrzej has chaired the International Probiotic Association (IPA) Technical Committee and has been a member of the IPA Board of Directors since early 2024. He also contributes to the IPA Postbiotics Committee and has served as the IPA expert liaison with the International Organization for Standardization (ISO) TC34/SC9 Working Group 11 since 2022, co-convening their Enumeration Subgroup.

Andrzej is dedicated to advancing the biotics industry by setting rigorous standards and driving innovation with a focus on quality.

Outside of his professional and scientific achievements, Andrzej is a member of the Eurofins Madison Site Employee Engagement Team and manages the Community Supported Agriculture (CSA) Program for the site. A founding member of the funk band Steez, he also plays saxophone, synthesizers, and vocals. Andrzej enjoys the outdoors, spending time with his family, and pretending to be a coffee aficionado. Additionally, he has a passion for collecting sneakers and fitted hats.

 

Below are resources from Andrzej:



Ensuring the safety, quality, and authenticity of dietary supplements has become increasingly complex in today’s global marketplace. To protect consumers and brands alike, robust quality systems, third-party certifications, and traceability measures are essential. This webinar highlights key integrity challenges facing the dietary supplement industry, from misleading claims to adulteration concerns, and advanced analytical solutions that address them.


Join us for a focused session on Eurofins’ new Product Certification program—designed to set a higher standard for quality and transparency across the dietary supplement, food, and retail industries. Learn why certification matters, how the process works, and what makes Eurofins uniquely qualified to deliver a seal backed by nearly 100 years of testing expertise.


The Innovative FEED Act proposes a modernized regulatory pathway for these zootechnical animal food substances, reclassifying them as food additives and enabling approval through the Food Additive Petition (FAP) process. This webinar provides insights from Eurofins’ experience navigating veterinary product development and highlight how legislative reform can unlock the next generation of feed solutions.


As global demand for animal protein continues to rise, producers, distributors, and suppliers face increasing pressure to meet complex veterinary drug compliance standards. This webinar offers a practical roadmap for navigating the regulatory landscape governing the export of animal protein, with a focus on FDA and USDA requirements, international certification processes, and emerging trade dynamics.


In this webinar, our experts will discuss the latest international regulations, the impact of recycled materials, and how proactive testing strategies can keep your packaging safe and compliant. Originally Recorded on September 17, 2025


With the release of the Make America Healthy Again (MAHA) report, the food and supplement industries are facing a pivotal moment. Join two of our leading experts as they unpack the report’s findings and explore what they could mean for consumer-packaged goods (CPG) companies. From reformulation strategies to enhanced ingredient scrutiny, this session will help industry professionals prepare for a wave of potential changes. Originally Recorded on August 21, 2025


The demand for speed in food production and distribution continues to increase, driven by consumer expectations for freshness, short product shelf lives, and regulatory compliance requirements. In this environment, rapid pathogen detection methods have become essential tools for timely decision-making and effective food safety management. This webinar will provide a technical overview of commercially available rapid methods for detecting key foodborne pathogens, including Salmonella, Listeria spp., and L. monocytogenes. Originally Recorded on August 20, 2025.


In this webinar, we cover our approach to custom method development with a focus on chromatographic techniques, such as GC-FID, GC-MS(MS), HPLC, UPLC, and HPLC-MS(MS). From the initial steps of deciding on an approach, to actual lab development and method validation for routine or regulatory use will be explained using actual case studies and examples. Originally Recorded on August 12, 2025


Accurate determination of creatine and its degradation product, creatinine, in raw materials and finished products is essential for quality control and regulatory compliance. This webinar will provide an overview of best practices in HPLC creatine and creatinine testing in diverse range of products, including protein powders, pre-workout formulations, beverages, and gummies. Originally Recorded on August 8, 2025


Issues during the Clean-In-Place (CIP) process, such as insufficient rinsing, can lead to the contamination of products, resulting in quality and/or safety concerns. This on-demand webinar covers various strategies for the detection of CIP chemicals in foods, beverages, and related products. Originally Recorded on June 25, 2025


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