Full-Time

Quality Engineer

Multiple Teams

Posted on 9/28/2025

Abbott

Abbott

10,001+ employees

Global healthcare company manufacturing medical devices

Compensation Overview

$60k - $120k/yr

Elkhart, IN, USA

In Person

Office/site: Building 01A, Sturgis, MI, USA. Travel: No. Division: ANSC Nutrition Supply Chain. Job family: Operations Quality. Location context: Abbott Nutrition site in Sturgis, MI.

Category
QA & Testing (1)
Required Skills
Data Analysis
Requirements
  • Bachelor’s Degree plus 2-5 years of relevant experience in Quality Assurance, Manufacturing or Engineering experience OR Master’s Degree plus 1-3 years of relevant experience in Quality Assurance, Manufacturing or Engineering
  • Demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA, GMP
  • Strong project management and leadership skills
  • Advanced computer skills, including statistical/data analysis and report writing skills. Experience implementing various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing)
  • Ability to leverage and/or engage others to accomplish projects
  • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
  • Multitasks, prioritizes and meets deadlines in timely manner.
Responsibilities
  • Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements
  • Lead, coach, and mentor non-exempt and entry level exempt personnel
  • Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues
  • Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues
  • Design and conduct experiments for process optimization and/or improvement
  • Appropriately document experiment plans and results, including protocol writing and reports
  • Lead process control and monitoring of CTQ parameters and specifications
  • Lead and implement various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing)
  • Lead the investigation, resolution and prevention of product and process nonconformances
  • Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member)
  • Lead in the completion and maintenance of risk analysis
  • Work with design engineering in the completion of product verification and validation
  • Work with microbiology to ensure appropriate environmental monitoring and that microbiology requirements are considered in product and process development activities
  • Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
Desired Qualifications
  • Experience working in a broader enterprise/cross-division business unit model
  • ASQ Certified Quality Engineering Certificate

Abbott develops and sells medical technologies and health solutions across cardiovascular care, diabetes management, diagnostics, nutrition, and neuromodulation. Cardiovascular devices help manage heart health; diabetes products enable glucose monitoring; diagnostic tests provide timely results; nutrition products support health; neuromodulation therapies target the nervous system to relieve pain or aid movement. It differentiates itself with a broad, integrated portfolio and a focus on accessibility and affordability of technologies worldwide. Its goal is to improve global health and well-being by delivering life-changing technologies that are accessible and affordable.

Company Size

10,001+

Company Stage

IPO

Headquarters

Lake Bluff, Illinois

Founded

1888

Simplify Jobs

Simplify's Take

What believers are saying

  • Exact Sciences acquisition completed March 2026 expands oncology diagnostics, accessing 600,000+ annual cancer screening patients.
  • Ultreon 3.0 targets 600,000+ complex PCI procedures annually in U.S., capturing high-volume interventional cardiology market.
  • Jenil Sheth's marketing leadership integrates cardiology, oncology expertise to cross-sell Exact Sciences to existing patient base.

What critics are saying

  • COVID-19 testing revenue decline limits diagnostics growth to 3.8% organic Q4 2025, excluding COVID headwinds.
  • Exact Sciences $23B acquisition dilutes 2026 EPS by $0.20, reducing guidance to $5.38–$5.58 midpoint.
  • Dexcom's advanced CGM sensor technology threatens FreeStyle Libre market share in diabetes care segment.

What makes Abbott unique

  • FreeStyle Libre achieved $2B Q4 2025 sales with 15% YoY growth, dominating continuous glucose monitoring.
  • Ultreon 3.0 AI-powered coronary imaging received FDA clearance April 2026, enabling precision-guided interventions.
  • Medical Devices segment achieved 12th consecutive quarter of double-digit organic growth through Q4 2025.

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Benefits

Health Insurance

401(k) Retirement Plan

401(k) Company Match

Flexible Work Hours

Remote Work Options

Paid Vacation

Paid Sick Leave

Paid Holidays

Professional Development Budget

Wellness Program

Company News

MedTech Markets
Apr 29th, 2026
Abbott receives FDA clearance/ce Mark for AI-powered Ultreon 3.0.

Abbott receives FDA clearance/ce Mark for AI-powered Ultreon 3.0. April 29, 2026 | MedTech News Alert (April 28, 2026) Abbott announced FDA clearance and CE Mark approval for its next-generation, artificial-intelligence (AI)-powered coronary imaging platform - the Ultreon 3.0. The new platform incorporates optical coherence tomography (OCT) that provides physicians real-time planning guidance during minimally invasive percutaneous coronary intervention (PCI) to open blocked coronary arteries. Ultreon 3.0 technology allows physicians to use OCT images to more clearly view a patient's arterial blockages using AI technology. AI assesses the type of plaque causing the blockage and assists the physician in choosing the best location and size of the stent for optimal improvement in blood flow. Ultreon 3.0 features advanced software providing one-second OCT pullback - a high-speed infrared light-based imaging technique - capable of capturing detailed cross-sectional views of the coronary artery and offering higher resolution readings compared to traditional intravascular ultrasound (IVUS) that has low or zero contrast. (Limiting use of contrast may be important for some patients, such as those with kidney disease.) According to Abbott, a summary of core benefits of the Ultreon 3.0 AI-driven software include: * A clear understanding of the size, shape, and location of a coronary blockage, allowing optimal stent placement to maximize blood flow and guide treatment planning. * A post-procedure assessment to ensure the stent improved blood flow in the artery. * A streamlined setup and enhanced AI-automated insights that simplify physicians' workflow. * Easily acquired images from inside blood vessels and ability to efficiently plan procedures, specifically tailored for patients with complex coronary disease. Comments from Abbott's chief medical officer of the company's vascular business, Ethan Korngold, M.D.: "Complemented by our leading coronary portfolio, Ultreon 3.0 makes OCT imaging more intuitive and powerful for physicians, reimagining imaging into a tool for precision-guided intervention before and after procedures. Advancements like Ultreon 3.0 showcase Abbott's leadership in AI-powered imaging and as a trusted partner in delivering smarter, more personalized coronary care." According to Abbott, complex PCI is a specialized procedure performed in more than 600,000 patients annually in the U.S. and is used to treat severe coronary artery disease involving the treatment of challenging lesions - or plaques - that have built up in a patient's coronary arteries. Some patients may require multiple stents to address lesions.

The Edge Malaysia
Apr 10th, 2026
Jury orders Abbott to pay US$53 mil in pre-term infant formula trial, says Chicago Tribune

Jury orders Abbott to pay US$53 mil in pre-term infant formula trial, says Chicago Tribune. 10 Apr 2026, 12:11 pm A Chicago jury is said to have ordered Abbott Laboratories to pay Abbott Laboratories US$53 million (RM210.98 million) in compensation to a group of families over its infant formula milk which can allegedly cause a potentially deadly bowel disease. CHICAGO (April 10): A jury in Chicago on Thursday said Abbott Laboratories must pay US$53 million (RM210.98 million) in compensatory damages to a group of families that had accused the company of failing to warn that its formula for premature infants can cause a potentially deadly bowel disease, according to the Chicago Tribune. The verdict came at the end of a lengthy trial in Cook County circuit court, the latest among hundreds of lawsuits alleging that Abbott's cow's milk-based formula products for pre-term infants can cause necrotising enterocolitis, or NEC. Four families' lawsuits were consolidated for trial. The jury will meet again on Friday to determine how much Abbott must pay in punitive damages, according to the Tribune. A spokesperson for Abbott did not immediately respond to a request for comment. Abbott has denied that the products, which it says are essential for premature babies when their mothers cannot produce enough breast milk, cause NEC. NEC, which causes the death of bowel tissue, mostly affects premature newborns and has an estimated mortality rate of more than 20%. The children, who were born in Chicago-area hospitals between 2012 and 2019, developed NEC but survived, according to their lawsuits. Three required surgery, and all live with ongoing health problems, according to the filings. Hundreds more lawsuits. Nearly 1,000 lawsuits have been filed against Abbott, which makes Similac formulas, and Enfamil manufacturer Mead Johnson, a unit of Reckitt. More than 700 of the cases are centralised in an Illinois federal court, with others pending in state courts in states including Illinois, Missouri and Pennsylvania. The products in question are cow's milk-based formula and products for fortifying mother's milk that are specially made for infants in hospital settings, not ordinary formula available to consumers in stores. Illinois-based Abbott also makes medical devices, adult and child nutrition products and medicines. The companies have said that while breast milk protects against NEC, their formulas do not cause it, and that the benefits of breast milk have long been known to clinicians. Abbott CEO Robert Ford suggested in 2024 that the pre-term products might become unavailable because of the litigation. US regulatory agencies and a working group of scientists convened by the National Institutes of Health said in a joint report in 2024 that current evidence supports the hypothesis that it is the absence of breast milk rather than exposure to formula that is associated with an increase in incidence of NEC. Trial results mixed. The companies have had a mixed record in the few cases to go to trial thus far. In 2024, a jury in St Clair County, Illinois ordered Mead Johnson to pay US$60 million to the mother of a premature baby who died after being fed the company's Enfamil baby formula. A few months later, a St Louis jury ordered Abbott to pay US$495 million in damages in another case. Both verdicts have been appealed. The American Academy of Pediatrics filed a brief supporting Mead Johnson in its appeal of the verdict against it last year, saying that formula is part of the standard of care for premature babies. Abbott and Mead Johnson prevailed in one trial in Missouri state court in October 2024, but the judge in that case ordered a new trial after finding that lawyers for the defendants had acted improperly. That ruling is also on appeal. In March, a Florida state judge dismissed a NEC case slated for an upcoming trial after finding that an additional warning to the family's doctors would not have changed their decision to use the formula. No cases have proceeded to trial in federal court, as the judge overseeing that litigation has dismissed three of the four cases selected for bellwether trials. In the most recent dismissal in October, the judge said that Abbott had presented substantial evidence on the need for the formula and shown the plaintiffs' proposed alternative was unfeasible. Uploaded by Felyx Teoh

The Outlook Online
Apr 10th, 2026
Keller Postman secures $70 million in verdicts for all four plaintiffs in historic Abbott formula trial.

Keller Postman secures $70 million in verdicts for all four plaintiffs in historic Abbott formula trial. PR Newswire Today at 3:41pm PDT CHICAGO, April 10, 2026 /PRNewswire/ - Keller Postman has secured a jury verdict of $70 million for four infants who suffered necrotizing enterocolitis ("NEC") as a result of being fed Similac Special Care. Defendant Abbott Laboratories, which manufactures Similac Special Care, was held liable by a unanimous jury for the defective design of its product, for failing to warn of the risk of NEC posed by it, and for the company's negligence leading to the infants' injuries. "The jury's verdicts on behalf of these four infants confirm once again what Abbott has known for years and chosen to ignore: that Abbott's cow's milk-based formula causes NEC in premature infants, often with devastating and irreversible consequences. Four families walked into that courtroom asking for justice, and four families received it. We are so proud to have stood beside them, and we are not done," said Ben Whiting, Senior Partner at Keller Postman. "For decades, Abbott Laboratories has shown a flagrant disregard for the health of the most fragile infants," said Amelia Frenkel, Partner at Keller Postman. "We hope that this verdict is a wakeup call to the company: Business as usual cannot continue. Safety has to come first for every preterm baby born today and tomorrow and into the future." The four cases were filed on behalf of four pre-term babies born at Chicago-area hospitals. They are among more than 1,700 lawsuits Abbott faces nationally over whether its cow's milk-based preterm infant formula causes NEC - a life-threatening condition in which tissue lining the intestine becomes inflamed and dies. This is the first time Abbott has faced a verdict in Illinois state court. Today's verdict builds on Keller Postman's landmark 2024 victory - a $60 million jury verdict against Mead Johnson, the first trial ever to hold a cow's milk-based formula manufacturer accountable for causing NEC in premature infants. Together, these outcomes send an unmistakable message: manufacturers who have long known of the dangers of their products and continued to market them to the most vulnerable infants will be held accountable. Keller Postman is representing thousands of families across the United States, with cases filed in Illinois, California, Florida, Pennsylvania, and Missouri. The firm will continue to litigate aggressively to ensure that its clients receive just compensation and that future parents are fully informed that breast milk, donor milk, and human milk-based formulas offer safer alternatives to defendants' products for preterm infants. Keller Postman's attorney team includes partners Ben Whiting and Amelia Frenkel, counsel Jamie Price, and associate Laura Shannon. At trial, they were joined by an Olson Grimsley trial team including Sean Grimsley, Kenzo Kawanabe, Abigail Hinchcliff, and Samara Hoose. About Keller Postman: Keller Postman is a national law firm dedicated to representing plaintiffs in the largest and most significant mass actions in the country. The firm's first-class legal team committed case managers, and tech-forward approach to complex litigation allow Keller Postman to outwork and out-innovate the other side. Its attorneys consistently deliver justice to families, consumers, veterans, and others injured by powerful defendants. SOURCE Keller Postman LLC This is a paid placement. For further inquiries, please contact PR Newswire directly.

MedTech Dive
Apr 10th, 2026
Pulse Biosciences hires Liane Teplitsky as COO.

Pulse Biosciences hires Liane Teplitsky as COO. The appointment gives a former Abbott leader oversight of efforts to bring a pulsed field ablation device to market. Published April 10, 2026 Name: Liane Teplitsky New title: Chief operating officer, Pulse Biosciences Previous title: CEO, Artedrone Pulse Biosciences has appointed Liane Teplitsky as chief operating officer, giving the former Abbott employee a key role in efforts to develop and launch a pulsed field ablation device. In March, Pulse committed to spending most of its R&D budget on the nPulse Cardiac Catheter, a PFA device for treating atrial fibrillation. Encouraged by first-in-human data on 150 patients in Europe, the company decided to cut investment in a surgical clamp program and spending on sales and marketing in support of its percutaneous soft-tissue ablation system. As COO, Teplitsky will lead Pulse's clinical, regulatory, quality and commercial functions as the company executes its new strategy. Pulse CEO Paul LaViolette said in a statement that Teplitsky's experience will be instrumental in accelerating the company's strategic priorities. Teplitsky most recently served as CEO of Artedrone, the developer of an autonomous robotic technology for stroke treatment. Affluent Medical recently acquired Artedrone and merged it with Caranx Medical to create Carvolix. Affluent CEO Sébastien Ladet took the top job at Carvolix. Before joining Artedrone, Teplitsky worked as president of global robotics, technology and data solutions at Zimmer Biomet. Teplitsky spent almost 10 years at Abbott and St. Jude Medical before joining Zimmer. The executive's career at the companies, which merged in 2017, included roles in cardiovascular disease and electrophysiology. At Pulse, Teplitsky will oversee a pivotal nPulse Cardiac Catheter trial in the U.S. and Europe, plus planned regulatory filings. The Food and Drug Administration approved the trial last year. Pulse enrolled the first patients this month. Pulse is assessing the device's safety and ability to isolate all targeted pulmonary veins in about 215 drug-resistant, symptomatic, paroxysmal atrial fibrillation patients. To support the trial, Pulse has expanded Chief Medical Officer David Kenigsberg's role at the company. Kenigsberg will maintain his active routine clinical practice while providing "increased leadership capacity" at Pulse as the company runs the pivotal trial. Teplitsky and Kenigsberg form part of a C-suite that began to take shape early last year, when LaViolette became CEO and Jon Skinner joined as CFO. The appointments followed a period of leadership turnover at the company.

Sports Insight
Apr 7th, 2026
Shokz to power six of the 2026 Abbott World MARATHON Majors Races as Official Headphone Partner.

Shokz to power six of the 2026 Abbott World MARATHON Majors Races as Official Headphone Partner. 0 67 2 minutes read * Shokz confirms that it will be the official headphone partner for six 2026 Abbott World Marathon Majors Races, including the TCS London Marathon * The partnership has been announced alongside all-new 'Chasing Stars' initiative, designed to support runners and give them the opportunity to participate in six of Abbott World Marathon Majors Races where Shokz is the official headphone partner. * As part of the Chasing Stars marathon initiative, Shokz has launched a range of marathon-exclusive OpenRun Pro 2, including a special TCS London Marathon Co-branded Edition London, April 2026 - Shokz, the pioneer of open-ear audio, has been appointed Official Headphone Partner of six Abbott World MarathonMajors Racesin 2026, including the Boston Marathon(R) presented by Bank of America, TCS London Marathon, TCS Sydney Marathonpresented by ASICS, BMW BERLIN-MARATHON, Bank of America Chicago Marathon, and TCS New York City Marathon, making Shokz the first brand to partner across six Majors. To mark this milestone, Shokz is launching Chasing Stars, a global runner recruitment programme that is now open for applications, with 200 runners set to be selected worldwide. Of those chosen, 50 runners will receive entries to six Abbott World Marathon Majors Races with which Shokz has partnered, offering a unique opportunity to take part in some of the world's most exciting events. The programme is designed to support everyday runners throughout their marathon journey, from training through to race day, and includes access to exclusive race kits, Shokz headphones and opportunities to participate in future race events. As part of the Chasing Stars launch, Shokz is introducing its first-ever OpenRun Pro 2 TCS London Marathon Co-branded Edition, alongside additional co-branded editions for each of the six Abbott World Marathon Majors Races with which Shokz has partnered. Marking Shokz's second year of TCS London Marathon sponsorship, the London edition features a distinctive deep blue and gold design with London-specific detailing, offering runners both a high-performance training companion and a meaningful keepsake. The marathon-exclusive OpenRun Pro 2 range will be available to purchase ahead of race day via local Shokz websites and at race expos where Shokz serves as the Official Headphone Partner. Backed by Shokz Global Ambassador Eliud Kipchoge and Global Athlete Eilish McColgan, Chasing Stars draws inspiration from the Six Star Finisher tradition. The initiative brings the full marathon journey to life, from training through to race day, spotlighting real runners from around the world and reinforcing a simple idea: running is about chasing your own goal, your own way. Runners in the UK can apply to join Chasing Stars via the Shokz website at uk.shokz.com. JD, the leading retailer for youth fashion and sportswear brands unveils their spring campaign. Saucony to deliver its RUSH depot to shoreditch for London Marathon week. SPORTSSHOES.COM LAUNCHES 'COUCH TO £5k' CHALLENGE AT FLAGSHIP RUNNING EXPERIENCE STORE ON SHOREDITCH HIGH STREET, LONDON. Crews unveiled for the CHANEL J12 boat race 2026 as channel 4 confirm debut broadcast will be presented by clare balding. Nike and WSL football launch New data-driven era in women's football, powered by sportable.

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