Full-Time
Global healthcare company manufacturing medical devices
$61.3k - $122.7k/yr
Remote in USA + 2 more
More locations: Chesapeake, VA, USA | Norfolk, VA, USA
Hybrid
Local candidates should reside in Chesapeake, Norfolk, or Suffolk; relocation is not offered. The territory includes Southern Virginia and North Carolina, with 2–3 hours of driving and 1–2 overnight stays per month.
Bachelor's
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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
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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
Avricore grants options. VANCOUVER, British Columbia, Aug. 28, 2026 (GLOBE NEWSWIRE) - AVRICORE HEALTH INC. (TSXV: AVCR) today announces that the Company's board of directors has approved the granting of stock options (the "Options") exercisable for a total of 3,300,000 common shares to its directors, officers, employees and consultants at an exercise price of CAD $0.06 per common share. All Options were granted pursuant to the Company's stock option plan and are subject to the terms of the applicable grant agreements and the requirements of the TSX Venture Exchange. The options shall vest quarterly commencing on the date of grant. The options expire 5 years from the date of the grant, subject to the optionees continuing to act as directors, officers, employees or consultants of the Company. Avricore's wholly-owned subsidiary, HealthTab Ltd, recently entered into a formal collaboration agreement with Abbott, a global healthcare company, to supply and distribute Abbott's point-of-care testing products through the HealthTab(TM) platform in the UK (news release dated August 20, 2026). HealthTab(TM) at the Core of Scalable, Integrated PoCT HealthTab(TM) provides a complete, turnkey solution underpinning national pharmacy-based PoCT networks, including best-in-class instruments, consumables, onboarding, training, and ongoing support for participating sites. At its centre is a secure cloud-based platform that seamlessly connects point-of-care analyzers, patient results, QC data, and pharmacist workflows, creating a unified digital infrastructure for community-based testing. This integrated approach ensures quality-assured testing, consistent data capture across locations, and real-time analytics to support public-health reporting and performance monitoring, while reducing implementation complexity for pharmacy partners. Commitment to Quality and Accuracy HealthTab(TM) is designed to meet the highest standards of analytical performance and reliability. Through its partnership with CEQAL Inc., a world-leading reference method laboratory and member of the CDC Cholesterol Reference Method Laboratory Network (CRMLN), HealthTab operates a comprehensive quality management program that mirrors the rigour of accredited clinical laboratories. This includes centralized lot monitoring of reagents, mandated internal quality control, and regular external quality-assessment (EQA) events, ensuring that results generated across every participating pharmacy are accurate, traceable, and consistent with internationally recognized reference standards. About Avricore Health Inc. Avricore Health Inc. (TSXV: AVCR) is a pharmacy service innovator focused on acquiring and developing early-stage technologies aimed at advancing pharmacy practice and patient care. Through its flagship offering HealthTab(TM), a wholly owned subsidiary, the Company's mission is to make actionable health information more accessible to everyone by creating the world's largest network of rapid testing devices in community pharmacies. Avricore Health Inc. Cautionary Note Regarding Forward-Looking Statements Information in this press release that involves Avricore Health's expectations, plans, intentions, or strategies regarding the future are forward-looking statements that are not facts and involve a number of risks and uncertainties. Avricore Health generally uses words such as "outlook," "will," "could," "would," "might," "remains," "to be," "plans," "believes," "may," "expects," "intends," "anticipates," "estimate," "future," "positioned," "potential," "project," "remain," "scheduled," "set to," "subject to," "upcoming," and similar expressions to help identify forward-looking statements. In this press release, forward-looking statements include statements regarding: the planned expansion of the HealthTab(TM) platform across UK pharmacy sites; the anticipated benefits of the collaboration with Abbott; the expected deployment of additional test assays; projected site deployment targets; and the Company's growth strategy in the UK. Forward-looking statements reflect the then-current expectations, beliefs, assumptions, estimates and forecasts of Avricore Health's management. The forward-looking statements in this press release are based upon information available to Avricore Health as of the date of this press release. Forward-looking statements believed to be true when made may ultimately prove to be incorrect. These statements are not guarantees of the future performance of Avricore Health and are subject to a number of risks, uncertainties, and other factors, some of which are beyond its control and may cause actual results to differ materially from current expectations, including without limitation: the ability of the parties to perform their obligations under the Agreement; failure to meet regulatory requirements; changes in the market; potential downturns in economic conditions; and other risk factors described in Avricore's public filings. These forward-looking statements speak only as of the date on which they are made, and the Company undertakes no obligation to update them publicly to reflect new information or the occurrence of future events or circumstances, unless otherwise required to do so by law. Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.
Dexcom and Abbott await Medicare CGM coverage expansion for non-insulin diabetes patients. Note* - All images used are for editorial and illustrative purposes only and may not originate from the original news provider or associated company. Two of the biggest names in diabetes technology - Dexcom and Abbott - are closely monitoring an anticipated Medicare CGM coverage expansion that could open access to continuous glucose monitors for millions of Americans with Type 2 diabetes who do not use insulin. A major policy shift on the horizon. Currently, Medicare coverage for continuous glucose monitors is restricted to individuals with Type 1 or Type 2 diabetes who either take insulin or have a documented history of problematic low blood sugar episodes. The Centers for Medicare and Medicaid Services is expected to broaden this coverage to include people with diabetes who do not take insulin - a move that both companies have indicated could meaningfully reshape the landscape for glucose monitoring in the United States. Dexcom CEO Jake Leach addressed the anticipated policy update during the company's late July earnings call, stating that the company expects to receive a response from the CMS before the end of the year, with coverage anticipated to go into effect by mid-2027. Scale of the opportunity for Dexcom. Dexcom estimates that approximately 25 million people in the United States have Type 2 diabetes and do not take insulin. Of that group, Leach noted that roughly half are of Medicare age. He described the CMS decision as having "the potential to completely reshape diabetes care in the U.S." To support the coverage expansion, Dexcom presented findings from a randomized, controlled trial earlier this summer at the American Diabetes Association's Scientific Sessions. The 26-week study demonstrated that participants using a CGM achieved a larger hemoglobin A1C reduction compared to a control group and spent five more hours per day within a normal glucose range. Dexcom reported second-quarter sales of $1.31 billion, reflecting a 13% increase year over year. Abbott's preparation and outlook. Competitor Abbott is equally positioned to benefit from the planned Medicare CGM coverage expansion. During Abbott's July earnings call, CEO Robert Ford told investors that the company expects the U.S. Type 2 expansion to make approximately 10 million additional Medicare recipients eligible for coverage, while also driving broader commercial insurance uptake. Ford confirmed that Abbott is actively preparing its sales force, distribution networks, and related resources ahead of the anticipated decision. "This could be a multibillion-dollar opportunity, and it could happen in the fall," Ford said. "I just can't forecast... when exactly it's going to happen." Abbott's diabetes care segment reported sales of $2.19 billion for the quarter, a 10.5% increase compared to the same period the prior year. With both Dexcom and Abbott reporting strong quarterly results in their respective diabetes care segments and preparing for what could be a significantly expanded patient base, the industry is keeping a close watch on CMS timelines. The Medicare CGM coverage decision, expected before year-end, is widely seen as a consequential development for the continuous glucose monitors market and for the broader diabetes management sector in the United States. Hospital & Healthcare Management brings together the global healthcare industry - from hospital administrators and clinical directors to health technology innovators and policy leaders - through trusted editorial, market intelligence, and digital engagement. Its 2026 Media Pack offers integrated solutions to reach your audience: * Magazine & Digital Editions Showcase your brand within premium healthcare industry coverage read by executives and decision - makers worldwide. * Industry Insights & Reports Align with data - driven analysis, trend reports, and regional roundups across the global hospital and healthcare management value chain. * Brand Authority & Credibility Position your company as a thought leader through expert commentary, interviews, and special features. - Never miss a story with notifications - Browse free from any location or device. Media Packs Expand Your Reach With Its Customized Solutions Empowering Your Campaigns To Maximize Your Reach & Drive Real Results! - Book a Conference Call
ABOT 1HCY26 profit rises 17%. MG News | August 28, 2026 at 10:17 AM GMT+05:00 August 28, 2026 (MLN): Abbott Laboratories (Pakistan) Limited (PSX: ABOT) reported a 17% increase in its net profit for the half-year ended June 30, 2026 (1HCY26), reaching Rs4.14bn compared to Rs3.54bn in the corresponding period last year. Reflecting this solid bottom-line growth, basic and diluted earnings per share (EPS) for the six-month period improved to Rs42.29, up from Rs36.19 in 1HCY25. The primary catalyst behind the financial expansion was a combination of steady local revenue growth and expanded gross margins. Net sales grew by 4% year-on-year to Rs38.03bn, up from Rs36.41bn in 1HCY25, as a 6% increase in local sales (Rs37.15bn) offset a 41% decline in export sales (Rs875.69m). Meanwhile, the cost of sales decreased slightly by 1% to Rs23.58bn, enabling gross profit to expand 15% to Rs14.45bn compared to Rs12.61bn in the prior year. On the operational front, overheads expanded to support distribution and administration. Selling and distribution expenses rose 11% to Rs6.15bn, administrative expenses grew 22% to Rs776.09m, and other charges increased 7% to Rs887.41m. Supported by a 43% boost in "other income", operating profit before finance costs rose 20% to Rs7.24bn. Below the operating line, finance costs remained minimal, dropping 5% to Rs35.64m. Although the company absorbed a minimum tax differential levy of Rs159.45m, profit before taxation grew by 17% to reach Rs7.04bn. The company absorbed an 18% higher net income tax expense of Rs2.90bn for the six-month period. Supported by local top-line strength, gross margin expansion, and higher secondary income, Abbott Laboratories (Pakistan) Limited securely closed the half-year with its net profit reaching Rs4.14bn. | STATEMENT OF PROFIT OR LOSS FOR THE HALF YEAR ENDED JUNE 30, 2026 (Rs.000) | | Description | 2026 | 2025 | change % | | Sales - net | / | / | / | | Local | 37,150,866 | 34,913,845 | 6.4% | | Export | 875,685 | 1,493,944 | -41.4% | | (Total net sales subtotal) | 38,026,551 | 36,407,789 | 4.4% | | Cost of sales | (23,576,445) | (23,792,889) | -0.9% | | Gross Profit | 14,450,106 | 12,614,900 | 14.5% | | Selling and distribution expenses | (6,145,400) | (5,527,267) | 11.2% | | Administrative expenses | (776,092) | (638,195) | 21.6% | | Other charges | (887,408) | (826,334) | 7.4% | | Other income | 593,980 | 416,745 | 42.5% | | Operating profit before finance costs | 7,235,186 | 6,039,849 | 19.8% | | Finance costs | (35,643) | (37,704) | -5.5% | | Profit before minimum tax differential and income tax | 7,199,543 | 6,002,145 | 19.9% | | Minimum tax differential | (159,446) | - | / | | Profit before income tax | 7,040,097 | 6,002,145 | 17.3% | | Current tax | (3,075,855) | (2,647,573) | 16.2% | | Deferred tax | 175,989 | 188,600 | -6.7% | | (Income tax subtotal) | (2,899,866) | (2,458,973) | 17.9% | | Profit for the period | 4,140,231 | 3,543,172 | 16.9% | | Earnings per share - basic and diluted (Rupees) | 42.29 | 36.19 | 16.9% |
Abbott has received CE Mark approval for its Amulet 360 Left Atrial Appendage Occluder, a next-generation device to reduce stroke risk in patients with atrial fibrillation. The device seals the left atrial appendage, potentially eliminating the need for long-term blood-thinning medication. Amulet 360 features a redesigned, softer body that conforms better to different anatomies than its predecessor. The VERITAS Study, involving 400 patients across more than 30 hospitals, showed the device was successfully implanted in 99.8% of patients. Complete closure with no significant leaks was achieved in 93.9% of patients by 45 days, with no complications reported within seven days post-implantation. First European cases were completed in Germany and Denmark. Abbott plans to expand availability across Europe in coming weeks. The device remains investigational in the US.
Abbott's Libre Duo 10 Day receives FDA authorization for continuous glucose and ketone monitoring. Abbott's Libre Duo 10 Day receives FDA authorization as the first wearable to continuously monitor glucose and ketone levels for people with diabetes. M.Pharm (Reg. Affairs) Abbott announced that the U.S. Food and Drug Administration (FDA) has authorized Libre Duo 10 Day, the first wearable device in the world to continuously monitor both glucose and ketone levels in a single system. The device is intended for people with diabetes aged 2 years and older and is designed to provide real-time glucose monitoring while detecting rising ketone levels that may signal an increased risk of diabetic ketoacidosis (DKA). Abbott plans to launch Libre Duo 10 Day in the United States later this year. First dual glucose-ketone monitoring system. Libre Duo 10 Day received FDA marketing authorization through the De Novo premarket review pathway after receiving Breakthrough Device designation. The FDA said the device is the first wearable in the United States to continuously monitor ketone levels and the first worldwide to continuously monitor ketones and glucose together. According to Abbott, the system is also the first to meet the FDA's integrated continuous glucose monitoring (iCGM) standard and the newly established integrated continuous glucose and ketone monitoring (iCGK) standard. How Libre Duo 10 Day works. The wearable continuously measures glucose and ketone levels in interstitial fluid beneath the skin every minute, day and night. Readings are transmitted wirelessly to a compatible smartphone, allowing users to view current glucose and ketone levels and their trends. The system can provide automatic alerts when ketone levels reach a concerning threshold. Unlike blood or urine ketone tests, which provide a single point-in-time measurement, Libre Duo 10 Day continuously tracks ketones and is designed to alert users when levels rise. The system provides up to 10 days of wear and is intended for people with diabetes aged 2 years and older, including those with type 1 or type 2 diabetes who use insulin or other glucose-lowering therapies such as SGLT2 inhibitors. Clinical evidence and DKA risk. The FDA's authorization was supported by six clinical studies involving more than 600 participants aged 2 years and older. These studies evaluated the accuracy of the system's glucose and ketone monitoring across a range of concentrations. The FDA reported that the device accurately tracked clinically meaningful differences in ketone levels throughout the 10-day wear period, including identifying elevated ketones before DKA developed. DKA can develop rapidly when insufficient insulin causes the body to break down fat for energy, resulting in potentially dangerous ketone accumulation. If untreated, DKA can progress to coma or death. Continuous ketone monitoring could provide earlier awareness of rising ketones compared with conventional point-in-time testing. Libre ecosystem and AID integration. Libre Duo 10 Day uses Abbott's latest-generation U.S. Libre app and integrates with the broader Libre digital health ecosystem, including LibreView for healthcare professionals and LibreLinkUp for caregivers. Abbott expects compatibility with Beta Bionics' iLet and Sequel Med Tech's twiist automated insulin delivery (AID) systems by the end of 2026, followed by devices from Insulet and Tandem in 2027. Abbott and MiniMed are also collaborating on integration with MiniMed smart dosing systems, expected in 2027. Safety and limitations. The FDA emphasizes that ketone information should be interpreted alongside glucose readings and symptoms. Abbott states that the Urgent High Ketones alarm may not detect every instance of ketone levels above 3.0 mmol/L. If readings or alarms do not match symptoms or expectations, users should follow the product's safety instructions and seek medical attention when appropriate. Abbott previously received CE Mark for Libre Duo and Libre Duo 10 Day in May 2026. The FDA authorization establishes a new category of continuous ketone-monitoring technology in the United States and expands the Libre platform beyond glucose monitoring, potentially enabling earlier recognition of ketone elevations associated with DKA. Reference. About the Writer Kalyani Boharapi (LinkedIn) is a pharmacy professional and healthcare writer currently pursuing an M.Pharm in Regulatory Affairs at Dr. D. Y. Patil College of Pharmacy, with interests in pharmaceutical regulations, drug development, and healthcare innovation. She has academic exposure to dossier preparation, scientific writing, and regulatory documentation. Kalyani has also completed certification courses in Generative AI, AI in Pharma, and Bioinformatics, and actively participates in pharmaceutical conferences to stay updated with emerging trends and advancements in the healthcare and pharmaceutical industry.