Full-Time

Manufacturing Service Technician 1

2nd Shift

Posted on 8/21/2026

bioMérieux

bioMérieux

5,001-10,000 employees

Global in vitro diagnostics for infectious diseases

Compensation Overview

$19.25 - $20/hr

+ Variable annual bonus

No H1B Sponsorship

Durham, NC, USA

In Person

Certification

Category
Operations & Logistics (1)
Required Skills
GMP
FDA Regulations
OSHA

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Requirements
  • Relevant experience in a regulated production or operations environment, or equivalent military experience.
  • High School Diploma, GED, or equivalent.
  • Ability to remain in a stationary position, often standing, for prolonged periods.
  • Ability to ascend and descend stairs, ladders, ramps, and similar structures.
  • Ability to wear personal protective equipment correctly for most of the workday.
  • Ability to operate heavy machinery.
  • Ability to adjust or move objects up to 50 pounds in all directions.
  • Ability to work extended and overtime hours as required to support production operations.
  • Ability to work 12-hour shifts, including weekends and potentially overnight shifts.
  • Ability to push and pull objects up to 150 pounds.
  • Satisfactory proof of identity and legal authorization to work in the United States is required for new hires.
Responsibilities
  • Assist with setting up, inspecting, performing preventive maintenance on, troubleshooting, and cleaning equipment used in manufacturing and packaging processes.
  • Complete production batches and corresponding documentation for associated tasks.
  • Perform AQL inspections, reworks, and material reconciliation associated with batches.
  • Operate high-speed, highly automated manufacturing equipment using HMI/SCADA interfaces.
  • Execute production activities according to approved Manufacturing Directions and job-related SOPs.
  • Complete batch paperwork accurately, thoroughly, and timely.
  • Perform and document processes and procedures in compliance with company and regulatory agency requirements.
  • Assist with reviewing and revising Manufacturing Directions and SOPs for manufacturing and packaging products.
  • Assist with manufacturing deviation analysis, CAPA actions, and other process equipment-related quality concerns.
  • Maintain work areas in an organized, clean, and tidy manner in compliance with cGMP requirements.
  • Operate cleaning equipment and record data manually or through designated software applications.
  • Perform self-audits of rooms and processes.
  • Train and certify teammates on production processes and procedures.
  • Generate reports, charts, and KPIs; interpret data to identify problems and make appropriate decisions.
  • Assist with executing validation and revalidation protocols for manufacturing and packaging equipment and procedures.
  • Perform computer applications.
  • Perform all work in compliance with company quality procedures and standards.
Desired Qualifications
  • Demonstrated proficiency operating high-speed, highly automated production equipment.
  • Knowledge of and experience following OSHA regulations, including LOTO and electrical safety.
  • Knowledge of FDA and/or GMP regulations.
  • Mechanical background.
  • Certification in a BioWorks Program or equivalent.
  • BioWorks, LEAN, or another Continuous Improvement Certificate.

bioMérieux provides medical diagnostics worldwide by developing, manufacturing, and selling diagnostic tests, instruments, and software that detect infectious diseases and antimicrobial resistance. Its products work by analyzing patient samples through diagnostic assays and integrated systems that combine reagents, specialized instruments, and software to produce actionable test results for healthcare providers, laboratories, and public health agencies. The company stands out from competitors through its global leadership in in vitro diagnostics, a broad portfolio of instruments, reagents, and software, and a strong emphasis on public health and antimicrobial resistance challenges. Its goal is to improve patient care and public health by delivering timely, accurate diagnoses that help guide treatment and curb the spread of infectious diseases.

Company Size

5,001-10,000

Company Stage

IPO

Headquarters

Marcy-l'Étoile, France

Founded

1963

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 organic sales grew 5%, and H1 free cash flow jumped 76%.
  • June 2026 SPINCHIP troponin approval expands immunoassays after last year's platform acquisition.
  • GENE-UP and SMARTBIOME launches broaden food and probiotic testing beyond clinical diagnostics.

What critics are saying

  • FDA classified 2026 VITEK recalls raise false-result exposure and retrospective-review costs now.
  • China fell 6% in H1 2026; management cut workforce there and lowered 2027-2028 targets.
  • Cepheid, Roche, and Abbott pressure molecular share as bioMérieux revises growth down.

What makes bioMérieux unique

  • BIOFIRE multiplex PCR anchors syndromic testing, with 2025 syndromic sales near 40%.
  • bioMérieux pairs instruments, reagents, software, and consultative workflows across microbiology and industrial QC.
  • The 2030 France BIOFIRE plant secures European supply and deepens manufacturing control.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401(k) Retirement Plan

401(k) Company Match

Adoption Assistance

Wellness Program

Employee Assistance Program

Commuter Benefits

Parental Leave

Employee Discounts

Company News

JSAN Publication
Aug 19th, 2026
Who owns Moderna right now in 2026?

Who owns Moderna right now in 2026? Moderna is publicly traded and widely held, not controlled by a family, state, or private equity sponsor. That makes who owns Moderna easier to see in filings, and it keeps control tied to the market rather than a single block holder. Moderna trades on the NASDAQ stock exchange under the ticker symbol MRNA and is a component of the S&P 500 index. The largest individual insider shareholders of Moderna are Stéphane Bancel (CEO) with approximately 7.3%, Noubar Afeyan (Co-founder and Chairman) with approximately 5%, Robert S. Langer (Co-founder) with approximately 4%, and Stephen Hoge (President) with approximately 1.3%. On the institutional side, the largest institutional shareholders of Moderna include Vanguard Group Inc., BlackRock, Inc., FMR LLC (Fidelity), Baillie Gifford & Co., State Street Corp., Capital World Investors, Geode Capital Management, and Morgan Stanley. No single person or entity controls Moderna outright. It is a widely distributed public company where the biggest voices are large index funds and asset managers - the same institutional giants that dominate most large American public companies. Ownership and key stakeholders table. The origin story: A conversation that changed medicine. Moderna was founded in 2010 by Noubar Afeyan, founder and CEO of Flagship Pioneering, in collaboration with Robert Langer, a professor of chemical engineering at MIT, and Derrick Rossi, a stem cell biologist, with the aim of developing messenger RNA (mRNA) therapeutics as a novel drug modality. The company originated from exploratory work within Flagship's VentureLabs, initially codenamed LS18, and was renamed Moderna Therapeutics to reflect its focus on modified RNA technologies. The spark was a meeting between Noubar Afeyan and Derrick Rossi, who had been doing breakthrough research on using chemically modified mRNA to reprogram cells. Noubar Afeyan met with Bob Langer and Derrick Rossi to review recent data on the use of chemically modified mRNA to reprogram adult human fibroblast cells into induced pluripotent stem cells. Noubar envisioned a different use of engineered mRNA as a new kind of medicine and launched within Flagship's VentureLabs group a month-long exploration which eventually led to Newco LS18, Inc. - which became Moderna. Stéphane Bancel, who had been Chief Executive Officer of the French diagnostics company bioMérieux SA, joined Moderna's board of directors in March 2011, and became its CEO in October 2011. Bancel was the operational genius who took a brilliant scientific idea and turned it into a scalable company. Under his leadership, Moderna secured partnerships, built laboratories, raised hundreds of millions of dollars, and survived years of skepticism from the broader scientific and investment community - many of whom believed mRNA medicine was too speculative to ever work. The COVID-19 moment that changed everything. For its first decade, Moderna was known only within the biotechnology world. Then came 2020 - and everything changed overnight. When SARS-CoV-2 emerged in early 2020, Moderna's scientists began designing a vaccine within days of the viral genome being published. The mRNA platform they had spent a decade building was perfectly suited for the task - because instead of growing virus in a lab to make a traditional vaccine, Moderna just needed to encode the spike protein instructions into mRNA and inject them. Moderna received an award from U.S. government agency BARDA for up to $483 million to accelerate development. It then announced a supply agreement with the U.S. government for an initial 100 million doses of its COVID-19 vaccine. The result was Spikevax - one of the first two mRNA COVID-19 vaccines in history - which achieved 94.5% efficacy in clinical trials and was authorized for emergency use by the FDA in December 2020. Almost overnight, Moderna went from a well-funded biotech startup to one of the most important companies in the world. The IPO and the Road to the S&P 500. Moderna became a public company through its 2018 IPO, which opened the cap table to public investors and shifted control from founders to shareholders. At the time of its IPO, Moderna had never had a single approved product. It went public purely on the strength of its mRNA platform and pipeline - an extraordinary level of investor conviction. The 2018 IPO raised approximately $600 million - the largest biotech IPO in history at that time. The underwriters priced shares at $23 each. By the peak of the COVID-19 vaccine rollout in 2021, MRNA shares had hit $497 - a gain of more than 2,000% in under three years. That surge created enormous paper wealth for the founders. Stéphane Bancel's net worth briefly exceeded $10 billion at the peak. Noubar Afeyan and Robert Langer also saw their stakes become worth billions. The Moderna story had become one of the greatest wealth-creation events in biotechnology history. Where is Moderna today in 2026? The post-COVID world has been a harder one for Moderna. Demand for COVID-19 vaccines has normalized dramatically, and the company has posted significant losses as it works to build out its broader pipeline. Moderna reported revenue of $1.94 billion in 2025, with a net loss of $2.8 billion and total assets of $12.3 billion. The company employs approximately 4,800 people. But Moderna's pipeline tells a more optimistic story. The company is advancing mRNA-based cancer vaccines - personalized treatments designed specifically for an individual patient's tumor - and has reported promising early results in trials with Merck. CEO Stéphane Bancel stated in early 2026: "I believe 2026 will also be the year when the world sees the promise of Moderna as a leading oncology company." In August 2026, the FDA approved Moderna's new mRNA-based flu vaccine - the first mRNA flu shot available to the public - marking another major milestone in the company's mission to use mRNA to fight a wide range of diseases beyond COVID-19. Frequently asked questions (faqs). Q1. Who owns Moderna in 2026? Moderna (NASDAQ: MRNA) is publicly owned with no single controlling shareholder - Vanguard and BlackRock are the largest institutional holders. Q2. Who founded Moderna? Moderna was founded in September 2010 by Noubar Afeyan, Robert Langer, Derrick Rossi, Kenneth Chien, and Timothy Springer, backed by Flagship Pioneering. Q3. Who is the CEO of Moderna in 2026? Stéphane Bancel is the CEO of Moderna, a role he has held since October 2011 after being recruited by co-founder Noubar Afeyan. Q4. What percentage of Moderna does Stéphane Bancel own? Stéphane Bancel owns approximately 7.3% of Moderna, making him the largest individual insider shareholder. Q5. When did Moderna go public? Moderna held its IPO in December 2018 on NASDAQ, pricing shares at $23 - the largest biotech IPO in history at that time. Q6. What is Moderna's revenue in 2025? Moderna reported $1.94 billion in revenue for 2025, with a net loss of $2.8 billion as it funds its broader pipeline beyond COVID-19 vaccines. Q7. Does the U.S. government own part of Moderna? No. The U.S. government funded Moderna's COVID-19 vaccine development through BARDA grants and supply agreements but holds no equity ownership in the company. Q8. What new products is Moderna launching in 2026? In August 2026, the FDA approved Moderna's first mRNA-based flu vaccine - and the company is advancing personalized mRNA cancer vaccines in partnership with Merck. Moderna is a publicly traded company on NASDAQ (ticker: MRNA) with no single controlling owner. It was founded in September 2010 by Noubar Afeyan, Robert Langer, Derrick Rossi, Kenneth Chien, and Timothy Springer - backed from day one by Flagship Pioneering, the venture capital firm that incubated the entire concept. The largest individual insider shareholders today are CEO Stéphane Bancel (~7.3%), Co-founder and Chairman Noubar Afeyan (~5%), and Co-founder Robert Langer (~4%). The biggest institutional holders are Vanguard, BlackRock, Fidelity, and Baillie Gifford. No single entity holds majority control - making Moderna a true public company, accountable to its broad shareholder base. From a codenamed startup experiment in 2010 to a COVID-19 vaccine that reached hundreds of millions of people, to an mRNA flu shot approved by the FDA in 2026 - Moderna's story is far from over.

PR Newswire
Aug 7th, 2026
bioMérieux highlights positive impacts of rapid, accurate diagnostics for Patients and accepts industry awards at ADLM 2026.

bioMérieux highlights positive impacts of rapid, accurate diagnostics for Patients and accepts industry awards at ADLM 2026. Aug 07, 2026, 14:10 ET SALT LAKE CITY, Aug. 7, 2026 /PRNewswire/ - bioMérieux, a world leader in the field of in vitro diagnostics, leveraged this year's 2026 Association for Diagnostics & Laboratory Medicine (ADLM) Annual Conference & Clinical Lab Expo for an important conversation about the impact of access to diagnostics while also accepting multiple IMV ServiceTrak(TM) awards. PRESS CONFERENCE The company hosted a press panel, The Power of Diagnostics: How Delays Impact Patients and Providers, to discuss the real-world impacts of delayed or inaccurate diagnostic answers for patients, providers, communities, and the healthcare system. Dr. Charles K. Cooper, Executive Vice President and Chief Medical Officer at bioMérieux, moderated the panel with: * Dr. Omai Garner, Clinical Professor and Director of Clinical Microbiology, UCLA; * Dr. Michael Astion, PhD, Medical Director, Regional Laboratories and Point of Care, Medical Director, Reference Laboratories and PLUGS (Patient-Centered Laboratory Utilization Guidance Services), Department of Laboratories, Seattle Children's Hospital, Professor of Laboratory Medicine and Pathology, University of Washington; * Helaine Bader, MPH Vice President of Education, HealthyWomen; and * Dr. John Hurst, Senior Director, Field Medical Affairs at bioMérieux. Dr. Cooper noted that the panel discussed the "tremendous amount of pressure health care systems face and how access to rapid diagnostics at the point of care often alleviates some of this stress by getting health care clinicians and their patients answers while they wait." "Delay in getting a diagnosis may result in patients not receiving treatment at all because they may not come back for follow-up," said Ms. Bader. "Faster time to diagnosis during a single visit not only provides the patient with immediate answers but also builds trust between the patient and provider and reduces patient frustration, potential complications from the infection and the need for repeat visits." INDUSTRY RECOGNITION During the show, bioMérieux also accepted seven 2026 IMV ServiceTrak(TM) Clinical Laboratory Awards. These awards highlight bioMérieux's continued commitment to delivering industry-leading diagnostic solutions and exceptional customer support to clinical laboratories. 2026 ServiceTrak Awards: ID/AST Systems * Best Customer Satisfaction * Best System Performance * Best Service 2026 ServiceTrak Awards: Blood Culture Systems * Best Customer Satisfaction * Best System Performance * Best Service 2026 Best System Performance * Immunoassay Analyzers "We are thrilled that IMV and the Science and Medicine Group has recognized bioMérieux for the ninth consecutive year for the continued dedication and excellence of our product management, operations, and customer support teams," said Randy Pritchard, General Manager and Sr. Vice President of Clinical Operations, bioMérieux. "This recognition, across our immunoassay, ID/AST Systems, and Blood Culture Systems offerings, highlights our commitment to pioneering diagnostics in the fight against sepsis and antimicrobial resistance." ABOUT BIOMÉRIEUX Pioneering Diagnostics A world leader in the field of in vitro diagnostics since 1963, bioMérieux is present in 46 countries and serves more than 160 countries with the support of a large network of distributors. In 2025, revenues reached €4.1 billion, with over 94% of sales outside of France. bioMérieux provides diagnostic solutions (systems, reagents, software and services) which determine the source of disease and contamination to improve patient health and ensure consumer safety. Its products are mainly used for diagnosing infectious diseases. They are also used for detecting microorganisms in agri-food, pharmaceutical and cosmetic products. www.biomerieux.com. bioMérieux is listed on the Euronext Paris stock market. Symbol: BIM - ISIN Code: FR0013280286 Reuters: BIOX.PA/Bloomberg: BIM.FP SOURCE bioMérieux

Ashland - Local Town Pages
Jul 14th, 2026
bioMérieux to Showcase Company's Latest in Diagnostic Innovations at ADLM 2026.

bioMérieux to Showcase Company's Latest in Diagnostic Innovations at ADLM 2026. PR Newswire Today at 8:43am PDT ANAHEIM, Calif., July 14, 2026 /PRNewswire/ - bioMérieux, a global leader in in vitro diagnostics, today announced it will showcase its latest diagnostic solutions and innovations at the 2026 Association for Diagnostics & Laboratory Medicine (ADLM) Annual Conference & Clinical Lab Expo, taking place in Anaheim, California, July 26 through 30. Attendees are invited to visit bioMérieux at booth #2501 in Hall B to explore the company's comprehensive portfolio and connect with experts across clinical microbiology, molecular diagnostics, and laboratory informatics. Featured Technologies at Booth #2501 This year's company presence is anchored by the theme: "A legacy of diagnostic leadership. Your partner for what's ahead." The theme reflects bioMérieux's continued commitment to advancing diagnostic excellence over the past 63 years, while supporting laboratories and healthcare practitioners in navigating the future of medicine. At the expo, bioMérieux will highlight a range of innovative platforms designed to showcase the company's end-to-end laboratory ecosystem including: BIOFIRE(R) FILMARRAY(R) TORCH System, a multiplex PCR technology that tests for a comprehensive group of targets in about an hour, BIOFIRE(R) SPOTFIRE(R) System, a multiplex PCR platform that brings reliable diagnostics to point-of-care clinical settings, VITEK(R) MS PRIME, a mass spectrometry system for routine microbial identification, and the VIDAS(R) 3, an automated benchtop immunoassay system. Visitors will be able to explore how bioMérieux's solutions connect microbiology, molecular diagnostics, laboratory automation, informatics, and stewardship initiatives to help laboratories improve efficiency, accelerate decision-making, and optimize patient care. In addition, visitors can explore bioMérieux's latest data and IT solutions, and Lab Consultancy offerings, designed to help laboratories optimize operations, improve outcomes, and drive digital transformation. Educational Symposiums As part of its commitment to advancing clinical knowledge and best practices, and demonstrating the value of diagnostics, bioMérieux will host two symposiums included in the conference's agenda: * From Central Lab to POC: Rethinking Vaginitis Diagnostics * Tuesday, July 28 from 12:00 p.m. until 12:20 p.m. in Exhibit Hall Theater 2 * Attendees will examine current diagnostic limitations, the consequences of delayed results, and how point-of-care testing aligns with real-time decision making. * The Syndromic Standard: Explore the Clinical Impact of MPCR GI Panels for Gastroenteritis * Tuesday, July 28 from 2:45 p.m. until 3:35 p.m. in Exhibit Hall Theater 1 * Attendees will learn about the latest developments in reducing diagnostic uncertainty, improving time-to-treatment, and advancing patient outcomes. Press Conference and Panel Discussion The company will also host a press conference panel, The Power of Diagnostics: How Delays Impact Patients and Providers, on Wednesday, July 29 from 9:00 a.m. until 9:45 a.m. in room 213D. Panel experts from bioMérieux, rural medicine, and patient advocacy will discuss the real-world impacts of delayed or inaccurate diagnostic answers for patients, providers, communities, and the healthcare system, especially as they affect women, minority communities, and other underserved populations. The panel will feature real-world examples from patient and provider experiences and potential solutions for today and the future. Conference attendees and members of the media are invited to attend. For media looking to register for event credentials: visit https://myadlm.org/media/press-registration. For more information on the bioMérieux press conference contact: [email protected]. ABOUT BIOMÉRIEUX Pioneering Diagnostics A world leader in the field of in vitro diagnostics since 1963, bioMérieux is present in 46 countries and serves more than 160 countries with the support of a large network of distributors. In 2025, revenues reached €4.1 billion, with over 94% of sales outside of France. bioMérieux provides diagnostic solutions (systems, reagents, software and services) which determine the source of disease and contamination to improve patient health and ensure consumer safety. Its products are mainly used for diagnosing infectious diseases. They are also used for detecting microorganisms in agri-food, pharmaceutical and cosmetic products. bioMérieux is listed on the Euronext Paris stock market. Symbol: BIM - ISIN Code: FR0013280286 Reuters: BIOX.PA/Bloomberg: BIM.FP SOURCE bioMerieux This is a paid placement. For further inquiries, please contact PR Newswire directly.

Nutrition Insight
Jul 13th, 2026
BioMérieux's new commercial DNA test rapidly screens dietary supplement label claims.

BioMérieux's new commercial DNA test rapidly screens dietary supplement label claims. Key takeaways. * BioMérieux has launched a new commercial DNA test that verifies probiotic dietary supplement label claims in under 90 minutes. * Developed with the natural products brand NOW, the on-site test identifies 18 common probiotic species to reduce operational costs and delays. * The system provides manufacturers and third-party labs with a rapid, standardized alternative or complement to traditional sequencing. Laboratory diagnostics specialist BioMérieux has launched Gene-Up Probiotic Species ID, a new solution for verifying dietary supplement label claims in less than 90 minutes, addressing the cost, complexity, and delays of traditional workflows. This new commercial DNA test allows internal quality teams and external labs to easily identify specific probiotic species in their own facilities. BioMérieux developed the system in collaboration with Now, a natural supplements brand with more than 50 years of experience in product testing. Now was previously reliant on third-party reference laboratories for multi-strain species identification on mixed formulations. It partnered with bioMérieux to develop a faster, more capable verification solution that prioritizes scientific rigor and operational efficiency. "Waiting weeks for compendial-based species identification created bottlenecks across our operations, from delayed production release to increased holding costs and unnecessary product risk," says Maria Mendres, microbiology manager at Now. "Our partnership with BioMérieux to develop Gene-Up Probiotic Species ID gives us, as well as the industry at large, the ability to generate accurate, on-site species-level results in 90 minutes or less." Mendres adds that this speed and accessibility have helped the brand hit production targets and minimize waste, while strengthening its ability to consistently deliver validated label claims. Traditional challenges of species-level identification. According to BioMérieux, demonstrating probiotic efficacy requires reliable species-level identification. However, it notes that many existing quality control approaches are costly, complex, or slow. This puts an operational strain on quality teams and limits routine testing. Gene-Up Probiotic Species ID accurately identifies 18 of the most commonly used probiotic species across capsules and powders in 90 minutes or less.The company stresses that these pressures are driving demand for faster, more practical testing solutions that support quality, transparency, and consistency without compromising scientific robustness. Gene-Up Probiotic Species ID accurately identifies 18 of the most commonly used probiotic species across capsules and powders, including Lactobacillus acidophilus, L. rhamnosus, and Bifidobacterium lactis, in 90 minutes or less. "Probiotic manufacturers are navigating a rapidly evolving landscape where ensuring reliable species verification is becoming essential, not only for quality control, but also for minimizing operational risk, supporting accurate label claims, and maintaining market access in a highly competitive category," says Alejo Migones, SVP of Global Food Safety & Quality at BioMérieux. Third-party screening applications. In addition to manufacturers, Gene-Up Probiotic Species ID has been adopted by third-party reference laboratories seeking to broaden their probiotic testing capabilities. Because the assays offer a rapid and standardized approach to bacterial species identification, they serve as a complementary option to sequencing for routine testing and high-throughput screening. The solution is designed for laboratory workflows and supports timely label verification. BioMérieux says this helps laboratories manage increasing sample volumes, while reserving sequencing resources for more complex analytical needs. BioMérieux's xPRO Program. This is the latest diagnostic innovation from BioMérieux's xPro Program, which connects industry leaders with BioMérieux partners to accelerate the development and commercialization of next-generation molecular diagnostics that solve pressing quality and safety challenges. BioMérieux operates in 46 countries and serves more than 160 countries with the support of a large network of distributors. The company offers diagnostic solutions that determine the source of disease and contamination in supply chains. Its products are mainly used for diagnosing infectious diseases. In addition to species identification with Gene-Up Probiotic Species ID, the company provides tools for detection, enumeration, and environmental monitoring. "In the US, where the probiotics market continues to grow, and consumer scrutiny continues to rise, Gene-Up Probiotic Species ID gives manufacturers the confidence to stand behind their products and deliver precise species identification that supports label integrity and protects brand reputation," says Miguel Villa, SVP of Industrial Applications, North America at BioMérieux. The launch follows a recent analysis of over 350 products from US drugstores, which found that probiotic supplements contain limited microbial diversity and lack a clear link to the intended health benefit. The authors of the study have created HaPaPro, a tool that identifies beneficial microbes using over 1,000 computer models.

PR Newswire
Jul 8th, 2026
bioMérieux launches 90-minute PCR test to verify probiotic species in supplements

bioMérieux has launched GENE-UP PROBIOTIC SPECIES ID, a PCR testing solution that verifies probiotic species in dietary supplements within 90 minutes. The system was developed with NOW, a natural products manufacturer, to replace slower traditional methods that could take weeks. The solution identifies 18 commonly used probiotic species in capsules and powders, including Lactobacillus acidophilus and Bifidobacterium lactis. It enables manufacturers to conduct in-house quality control testing and verify label claims more efficiently. The product is currently available only in the United States, with a global rollout planned. Third-party laboratories are also adopting the technology to expand their probiotic testing capabilities and manage higher sample volumes. The development is part of bioMérieux's xPRO Programme, which partners with industry leaders to create molecular diagnostics. bioMérieux, headquartered in France, reported €4.1 billion in revenue in 2025.