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Medline

Manufacturer and distributor of medical supplies

Quality Engineer - Advanced Wound Care

Full-Time
$79k - $119k/yr+ Bonus and/or incentive
Junior
Bachelor's
Northfield, IL, USA
Hybrid

About the job

Requirements
  • A Bachelor's degree in Engineering, Science, Math, or another related technical field is required.
  • At least 2 years of experience in Quality or Engineering is required.
  • Experience developing ways of accomplishing goals with little or no supervision, depending on oneself to complete objectives, and determining when escalation of issues is necessary.
  • Experience using time management skills to prioritize, organize, and track details in order to meet deadlines of multiple projects.
  • Experience problem solving, overcoming obstacles, and reaching a positive and successful solution through mathematical or systematic operations.
  • Experience using Microsoft Office Suite products, including Word, Excel, PowerPoint, and Outlook.
  • Intermediate skill in Microsoft Excel, including conditional formatting, tables, formulas, and charting.
  • Working knowledge of government and industry quality assurance codes and standards, including 21 CFR 820 and ISO 13485.
  • Position requires up to 15% travel.
Responsibilities
  • Independently set basic quality standards for in-process activities while leading efforts to develop methods for testing, sampling, and training.
  • Evaluate production processes and recommend improvements.
  • Qualify vendors and conduct vendor management.
  • Generate and maintain Device Master Records, product specifications, design control files, and CE technical files.
  • Manage the development and implementation of methods and procedures for process control, process validation, process improvement, testing, and inspection to ensure product quality and functionality.
  • Design experiments to understand sources of variation affecting products and processes.
  • Apply statistical process control methods to analyze data and evaluate current processes and process changes.
  • Design and perform experimental product testing and analysis to maintain quality levels and minimize defects and failure rates.
  • Generate and analyze reports and defective products to determine trends and lead corrective actions.
  • Use probability and statistical quality control concepts to guide decisions.
  • Direct and collaborate with supplier representatives on quality problems, ensure corrective action implementation, and contribute to supplier quality improvement programs.
  • Lead supplier qualifications.
  • Provide Quality expertise in Product Development, Design Control activities, Risk Management, and CE Technical Files.
  • Build appropriate product documentation, including Device Master Records, in compliance with applicable regulations.
  • Work with Regulatory Groups and Suppliers to produce 510(k) submissions and letters to file as required.
  • Coordinate product testing with internal and external laboratories as required.
  • Ensure compliance with domestic and international regulations associated with product lines and processes.
  • Perform quality reviews of design documentation for compliance with stated requirements, including vendor quality documents and company quality records.
  • Lead investigations of product and process non-conformances and out-of-specification results and develop effective corrective and preventive actions.
Desired Qualifications
  • At least 2 years of industry experience in Medical Devices, Drugs, and/or fields directly related to the role.

About the company

Medline Industries designs, produces, and distributes medical supplies for healthcare settings. It combines manufacturing and distribution to control product quality and sell directly to hospitals and other healthcare providers, offering a wide range of Medline-branded and third-party products. Its products include gowns, uniforms, gloves, and other medical consumables, produced and then delivered through a direct-to-provider model. The company differentiates itself with vertical integration that bypasses traditional distributors, a long-standing family-led culture that continued after a 2021 private-equity-led majority investment, and the scale to serve healthcare systems with a broad catalog. The goal is to supply healthcare providers with a comprehensive, high-quality catalog of medical products while expanding market reach and maintaining reliability through direct manufacturing-and-distribution control.

Company Size

10,001+

Company Stage

IPO

Headquarters

Northfield, Illinois

Founded

1966

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What believers are saying

  • August 5, 2026 sales rose 11.6% to $7.7 billion.
  • First-half 2026 new customer signings drove organic sales guidance to 9%-10%.
  • Tariff refunds added $243 million in Q2, boosting cash and EBITDA.

What critics are saying

  • FDA warning letters on June 2, 2026 cite contamination and cleaning failures.
  • August 2026 recall of neonatal breathing circuits exposes quality control gaps.
  • A second major quality breakdown could trigger consent orders, plant shutdowns, or delisting.

What makes Medline unique

  • Medline controls manufacturing and distribution, letting it sell directly to providers.
  • Its scale spans 45,000 employees and more than 100 countries.
  • Prime Vendor bundles products with clinical tools like Skin Health and NE1 Wound.

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Benefits

Health Insurance

Life Insurance

Disability Insurance

401(k) Company Match

Paid Vacation

Paid Sick Leave

Growth & Insights and Company News

Headcount

6 month growth

↑ 0%

1 year growth

↑ 0%

2 year growth

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DistilInfo
Sep 28th, 2026
James River Home Health selects Medline vendor.

James River Home Health selects Medline vendor. Medline announced it signed a new Prime Vendor agreement with James River Home Health & Hospice, a home health and hospice provider serving patients and families across its care network, a James River Home Health Medline Prime Vendor arrangement aimed at supporting the provider's growth. What the James River Home Health Medline Prime Vendor agreement includes. Through the agreement, James River gains access to Medline's medical-surgical product portfolio and distribution capabilities, intended to streamline ordering and timely, reliable delivery of supplies. The Prime Vendor model typically consolidates a provider's purchasing with one distributor, which can simplify logistics and standardize the products clinicians use. Clinical tools added to the arrangement. James River will also implement Medline's Skin Health Program and use the NE1 Wound Tool, which helps clinical staff assess and document wounds. Pairing supply purchasing with clinical programs suggests the agreement is meant to support care consistency as well as procurement. James River's rationale for the James River Home Health Medline Prime Vendor deal. David Gilligan, CFO of James River Home Health & Hospice, described the organization as a growing provider focused on expanding access to high-quality care. He said building infrastructure and partnerships to support clinicians and maintain consistency is a priority, and that Medline's scale, expertise, and post-acute focus make it a strong partner as James River serves more patients. Why consistency matters as providers grow. Expanding home-based providers often add clinicians and locations quickly, which can produce variation in the supplies and documentation practices staff use. Standardizing on a single vendor and shared tools is one way to keep practices uniform across a growing network. Medline's perspective on the James River Home Health Medline Prime Vendor agreement. Renee Fisher, senior vice president of national field sales for post-acute care at Medline, said the company is proud to work with James River as it expands access to home-based care. She said the combination of reliable product access and post-acute supply chain solutions is meant to let James River's teams stay focused on patients and families. About Medline. Medline describes itself as the largest provider of medical-surgical products and supply chain solutions serving all points of care, employing more than 45,000 people worldwide and operating in more than 100 countries. The company trades on Nasdaq under MDLN and is headquartered in Northfield, Ill. How the James River Home Health Medline Prime Vendor agreement fits home-based care trends. The announcement reflects a theme raised at recent home-based care events, where operators said growth must rest on operational infrastructure and discipline. Supply chain reliability, clinical documentation, and compliance are part of that backbone, particularly as federal fraud enforcement and documentation scrutiny continue to affect home health and hospice providers. Why Wound documentation is a notable detail. Wound assessment and documentation are areas where consistent records matter for both clinical care and payer or regulatory review. Providing a standard tool for staff may help James River document care uniformly, though the announcement did not describe outcomes or metrics. What the James River Home Health Medline Prime Vendor agreement means going forward. The agreement gives James River a single supply and clinical program partner as it grows, and it gives Medline another post-acute customer. Because financial terms, contract length, and the size of James River's network were not disclosed, the practical impact on costs and operations cannot be assessed from the announcement alone. What to watch going forward. Observers will likely watch whether James River reports operational or clinical results from the Skin Health Program and NE1 Wound Tool, and whether more home health and hospice providers pursue similar prime vendor and clinical program bundles. As a company announcement, the James River Home Health Medline Prime Vendor news is best read as a signal of provider growth and vendor consolidation in post-acute care rather than as evidence of measured performance gains.

GlobeNewswire
Sep 25th, 2026
MDLN Stock Drop alert: Medline Stock plummets 13% after product quality issues revealed - BFA Law notifies investors of its ongoing Securities Fraud investigation.

MDLN Stock Drop alert: Medline Stock plummets 13% after product quality issues revealed - BFA Law notifies investors of its ongoing Securities Fraud investigation. BFA Law is investigating whether Medline Inc. committed securities fraud relating to statements about Medline's manufacturing and product quality. NEW YORK, Sept. 25, 2026 (GLOBE NEWSWIRE) - Leading securities law firm Bleichmar Fonti & Auld LLP announces an investigation into Medline Inc. (NASDAQ:MDLN) for potential securities fraud after its significant stock drops. If you invested in Medline securities, you are encouraged to obtain additional information by visiting: https://www.bfalaw.com/cases/medline-class-action-lawsuit. Key Details of the Medline ($MDLN) Class Action Investigation: * Investigation Overview: Securities fraud relating to Medline's statements about its manufacturing and product quality. * Stock Declines: June 2, 2026 - 7% Stock Drop August 5, 2026 - 13% Stock Drop * Action: Contact BFA Law to discuss your rights Why is Medline Being Investigated for Securities Fraud? Medline is a healthcare manufacturing and supply-chain company that retails and distributes medical and surgical products. BFA is investigating whether Medline misled investors about its manufacturing and product quality. Why did Medline's Stock Drop? On June 2, 2026, the FDA published a warning letter detailing Medline's "significant violations of Current Good Manufacturing Practice regulations for finished pharmaceuticals" and stating that Medline "failed to thoroughly investigate any unexplained discrepancy or failure of a batch or any of its components to meet any of its specifications." Following that announcement, Medline shares fell approximately 7% on June 2, 2026. Then, before market hours on August 5, 2026, Medline acknowledged that at least some of remediation steps taken to address the issues in the FDA's warning letter had "result[ed] in earnings loss" during the company's 2Q26 earnings call. Following that announcement, Medline shares fell approximately 13% on August 5, 2026. What Can You Do? If you invested in Medline securities, you may have legal options and are encouraged to submit your information to the firm. All representation is on a contingency fee basis; there is no cost to you. Shareholders are not responsible for any court costs or expenses of litigation. The firm will seek court approval for any potential fees and expenses. Submit your information by visiting: Or contact: Why Bleichmar Fonti & Auld LLP? BFA is a leading international law firm representing plaintiffs in securities class actions and shareholder litigation. It has been named a top plaintiff law firm by Chambers USA, The Legal 500, and ISS SCAS, and its attorneys have been named "Elite Trial Lawyers" by the National Law Journal, "Litigation Stars" by Benchmark Litigation, among the top "500 Leading Plaintiff Financial Lawyers" by Lawdragon, "Titans of the Plaintiffs' Bar" by Law360 and "SuperLawyers" by Thomson Reuters. Most recently, The Legal 500 awarded BFA the most client satisfaction accolades of any plaintiff's securities litigation law firm, with clients noting: "[t]here is no better service provider in the practice area," "[t]he interest of the client is always front and center," and "[t]here isn't a better firm in this space." One testimonial described the firm as "nimble and entrepreneurial," with a "relentless focus on adding value for clients." Among its recent notable successes, BFA recovered over $900 million in value from Tesla, Inc.'s Board of Directors, as well as $420 million from Teva Pharmaceutical Ind. Ltd. Attorney advertising. Past results do not guarantee future outcomes.

Benzinga
Sep 8th, 2026
Kaplan Fox urges Medline Inc. (MDLN) investors to contact the firm about possible securities law violations.

Kaplan Fox urges Medline Inc. (MDLN) investors to contact the firm about possible securities law violations. Stock score locked: want to see it? Benzinga Rankings give you vital metrics on any stock - anytime. New York, New York-(Newsfile Corp. - September 8, 2026) - Kaplan Fox & Kilsheimer LLP is investigating potential securities violations against Medline Inc. ("Medline" or the "Company") (NASDAQ:MDLN). If you are a Medline investor and have suffered losses, or if you have information that could assist in the Medline investigation, you may CLICK HERE to contact us. You may also contact Kaplan Fox by emailing [email protected] or by calling (646) 315-9003. On June 2, 2026, the Federal Drug Administration ("FDA") published a warning letter dated May 28, 2026 addressed to Medline summarizing "significant violations of Current Good Manufacturing Practice regulations for finished pharmaceuticals[.]" The FDA further states that Medline "failed to thoroughly investigate any unexplained discrepancy or failure of a batch or any of its components to meet any of its specifications." Following this news, the price of Medline stock fell $2.56 per share, or 7.16%, to close at $33.19 per share on June 2, 2026. According to a June 3, 2026 Reuters article, the latest FDA warning letter relates to "violations of manufacturing quality standards" and is "the second such action against the (C) ompany in two months." Further, the Reuters article states that according to the FDA, "the Company failed to thoroughly investigate microbial contamination incidents in finished drug products and also cited inadequate cleaning practices." WHY CONTACT KAPLAN FOX? Kaplan Fox & Kilsheimer LLP is a nationally recognized law firm focused on complex litigation, with offices in New York, Oakland, Los Angeles, Chicago, and New Jersey. Founded in 1956, the firm has spent more than 50 years prosecuting securities, antitrust, and consumer protection actions in federal and state courts nationwide, recovering more than $10 billion for clients and the classes it has represented. Kaplan Fox is widely regarded as one of the nation's premier plaintiffs' securities litigation firms and has received recognition from Chambers and Partners, Benchmark Litigation, Super Lawyers, and Lawdragon. Serving as lead or co-lead counsel in many landmark cases, the firm has secured some of the largest recoveries in the history of securities litigation, including a $2.425 billion recovery on behalf of Bank of America shareholders in In re Bank of America - the largest recovery ever obtained for claims under Section 14(a) of the Securities Exchange Act - $800 million recovered for the Arkansas Teacher Retirement System and other pension funds in ATRS v. Allianz Global Investors, and a $475 million settlement in In re Merrill Lynch. For decades, Kaplan Fox has represented public pension funds, institutional investors, businesses, and individuals in high-stakes litigation. Through its successful advocacy and precedent-setting victories, the firm has helped shape important areas of securities and corporate law while advancing accountability and protecting investor interests. This press release may be considered Attorney Advertising in some jurisdictions under the applicable law and ethical rules. Past results do not guarantee future outcomes. If you have any questions about this investigation, please contact: Pamela A. Mayer KAPLAN FOX & KILSHEIMER LLP 800 Third Avenue, 38th Floor New York, New York 10022 (646) 315-9003 [email protected] Laurence D. King KAPLAN FOX & KILSHEIMER LLP 1999 Harrison Street, Suite 1501 Oakland, California 94612 (415) 772-4704 [email protected] Contacting or submitting information to Kaplan Fox & Kilsheimer LLP does not create an attorney-client relationship, nor an obligation on the part of Kaplan Fox to retain you as a client.

American Hospital Association
Sep 8th, 2026
FDA issues highest recall for certain breathing circuits, catheters, spinal cord stimulators.

FDA issues highest recall for certain breathing circuits, catheters, spinal cord stimulators. Sep 08, 2026 - 04:36 PM The Food and Drug Administration has identified Class I recalls of the following products: Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits and certain reprocessed electrophysiology and ultrasound catheters by Medline, and all unused Infinion CX Leads by Boston Scientific. The FDA also issued early alerts for other medical products: certain VentStar Resus Neo hoses by Draeger, and certain convenience kits and IV start kits by AVID Medical. Correction notices were issued for certain Medline convenience kits containing recalled BD ChloraPrep Applicators, as well as Portrait Mobile Monitoring Solutions devices by GE Healthcare. Additionally, voluntary recalls were issued for certain lots of intravenous fluids by American Regent and B. Braun Medical.

GlobeNewswire
Sep 3rd, 2026
Medline announces participation in the Morgan Stanley 24th Annual Global Healthcare Conference.

Medline announces participation in the Morgan Stanley 24th Annual Global Healthcare Conference. September 03, 2026 08:30 ET | Source: Medline Inc. NORTHFIELD, Ill., Sept. 03, 2026 (GLOBE NEWSWIRE) - Medline Inc. ("Medline") (Nasdaq: MDLN) today announced that Jim Boyle, chief executive officer, and Mike Drazin, chief financial officer, are scheduled to present at the Morgan Stanley 24th Annual Global Healthcare Conference in New York, NY, on Tuesday, September 15, 2026, at 12:20pm ET. A webcast of the presentation will be available on the Events page of Medline's Investor Relations website at ir.medline.com. A replay of the webcast will be available on Medline's Investor Relations website for 90 days following the event. About Medline Medline is the largest provider of medical-surgical products and supply chain solutions serving all points of care. Through its broad product portfolio, resilient supply chain and leading clinical solutions, Medline helps healthcare providers improve their clinical, financial and operational outcomes. Headquartered in Northfield, Illinois, the company employs more than 45,000 people worldwide and operates in more than 100 countries. To learn more about how Medline makes healthcare run better, visit www.medline.com. Contacts Investor Relations: Karen King Global Head of Investor Relations Patrick Flaherty Director, Investor Relations Media Relations: Ben Fox Vice President, Corporate Communications (224) 327-9999 [email protected] Recommended reading.