EX-99.1 2 exhibit9912024q4pressrelea.htm EX-99.1 Document
Exhibit 99.1
Media Release
qiagen_logo.jpg


QIAGEN delivers solid Q4 2024 growth ahead of outlook

Q4 2024: Net sales of $521 million (+2% actual rates, +4% constant exchange rates (CER) core growth); diluted EPS of $0.39 and adjusted diluted EPS of $0.61

Net sales of $525 million CER ahead of outlook for at least $520 million CER and
adjusted diluted EPS of $0.61 CER ahead of outlook for at least $0.60 CER

QIAstat-Dx, QuantiFERON and QIAcuity digital PCR continue double-digit growth pace

30.6% adj. operating income margin up 2.6 percentage points vs. 28.0% in Q4 2023

FY 2024: Exceeded outlook for sales and adj. EPS; adj. operating income margin improves 1.8 percentage points to 28.7%

Free cash flow rises 63% to $506 million

2025 outlook for about 4% CER sales growth (about +5% CER core sales growth) and adj. diluted EPS of at least $2.28 CER; targeting adj. operating income margin improvement of at least 150 basis points

Venlo, the Netherlands, February 5, 2025 - QIAGEN N.V. (NYSE: QGEN; Frankfurt Prime Standard: QIA) today announced financial results for the fourth quarter and full-year 2024.

Net sales for Q4 2024 increased 2% to $521 million compared to Q4 2023, while sales at constant exchange rates (CER) of $525 million rose 3% and were above the outlook for at least $520 million CER and core sales (excluding discontinued products such as NeuMoDx and Dialunox) rose 4% CER. The adjusted operating income margin improved by 2.6 percentage points to 30.6%, driven by efficiency gains and benefits from the NeuMoDx decision, enabling reinvestments into targeted growth initiatives. Adjusted diluted earnings per share (EPS) were $0.61, and CER results of $0.61 were above the outlook for at least $0.60 CER.

QIAGEN expects the solid growth pace in H2 2024 to continue in 2025. Net sales are expected to rise about 4% CER (and core sales growth of about 5% CER). Adjusted diluted EPS is expected to be at least $2.28 CER, driven by a goal to improve the adjusted operating income margin by at least 150 basis points to above 30% while absorbing lower non-operating income contributions than in 2024.

"Our teams at QIAGEN concluded 2024 with a solid performance in the fourth quarter, exceeding our outlook for net sales and profitability. These results underscore the resilience of our portfolio, with over 85% of sales coming from highly recurring revenues, and our focus on delivering solid profitable growth in an ongoing challenging environment," said Thierry Bernard, CEO of QIAGEN.

"Our solid sales growth in the second half of 2024 mirrors our plans for further strong growth in 2025 as we reconfirm our 2028 targets. QIAstat-Dx exceeded expectations with four FDA clearances for our syndromic testing system in 2024 and one already in 2025, coupled with over 660 placements in 2024 that was ahead of our target. QuantiFERON delivered 11% CER growth for 2024, with significant opportunities for further expansion since only 40% of the global latent TB testing market has so far been converted from the outdated skin test. QIAcuity also delivered solid growth despite challenging instrument purchase trends as we expanded digital PCR into clinical use in 2024 while expanding our presence with academia, pharma and other customers."




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"We are pleased with our 2024 results that featured strong free cash flow combined with solid sales growth and a significant increase in the outlook for adjusted EPS during the year thanks to operational profitability improvements. Our confidence in QIAGEN's future is reflected in the return of about $300 million to shareholders in January through a synthetic share repurchase. We remain well-positioned to execute on our 2028 commitments for solid profitable growth, supported by our differentiated portfolio and disciplined capital allocation that seeks to strengthen our business while increasing returns to shareholders," said Roland Sackers, CFO of QIAGEN.

Key figures
In $ millions
(Except EPS and diluted shares)
Q4FY
20242023Change20242023Change
Net sales521 509 %1,978 1,965 %
Net sales - CER525 %1,991 %
Operating income119 111 %98 410 -76 %
Net income88 98 -10 %84 341 -76 %
Diluted EPS$0.39 $0.42 -7 %$0.37 $1.48 -75 %
Diluted shares (in millions)224231225231
Adjusted operating income159 142 12 %567 529 %
Adjusted net income136 127 %491 477 %
Adjusted diluted EPS
$0.61 $0.55 11 %$2.18 $2.07 %
Adjusted diluted EPS - CER
$0.61 11 %$2.20 %
Please refer to accompanying tables in this release for full income statement information and a reconciliation of reported to adjusted figures.
Tables may have rounding differences. Percentage changes are to prior-year periods.

Sales: Q4 2024 results showed 3% CER sales growth compared to Q4 2023, and 4% CER core growth (excluding sales from discontinued products). Diagnostic solutions led the product groups with 10% CER growth (+12% core growth) and driven by QuantiFERON (+14% CER) and QIAstat-Dx (+25% CER). PCR and Genomics product groups also delivered higher sales, while Sample technologies saw a modest decline. Consumables and related revenues grew 4% CER over Q4 2023, while instrument sales declined 6% CER due to ongoing cautious customer capital spending trends throughout 2024. For FY 2024, net sales increased 1% CER - and core sales rose 2% CER - supported by improving growth trends in H2 2024 compared to results in H2 2023.

Operating income: In Q4 2024, operating income rose 8% to $119 million, and included $21 million of pre-tax charges related to ongoing efficiency measures including the discontinuation of NeuMoDx. Adjusted operating income increased 12% to $159 million, with the adjusted operating income margin improving to 30.6% of sales from 28.0% in Q4 2023. This was driven by efficiency gains across QIAGEN that enabled reinvestments into growth initiatives, along with benefits of the NeuMoDx decision. In terms of components, the adjusted gross margin rose to 67.1% of sales from 65.7% in Q4 2023 due to various factors such as higher production capacity utilization. R&D investments were 9.3% of sales in Q4 2024, up slightly from 9.0% in Q4 2023, and aligned with the FY 2024 target. Sales and marketing expenses decreased to 21.8% of sales from 23.1% in Q4 2023, while General and administrative expenses declined to 5.3% of sales from 5.6% in Q4 2023. For FY 2024, the adjusted operating income margin was 28.7% of sales, an increase of 1.8 percentage points from 26.9% in 2023.

EPS: Diluted EPS was $0.39 per share in Q4 2024 compared to $0.42 in Q4 2023. Adjusted diluted EPS for Q4 2024 were $0.61 ($0.61 CER), and above the outlook for at least $0.60 CER. The adjusted tax rate was 19% in Q4 2024, and consistent with the quarterly estimate. For FY 2024, adjusted diluted EPS increased to $2.18 ($2.20 CER) from $2.07 in 2023, reflecting the significant improvements in adjusted operating income during the course of the year compared to the initial outlook for at least $2.10 CER.
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Sales by product groups
In $ millions
Q4FY
2024
sales
2023
sales
Change
CER change
2024
sales
2023
sales
Change
CER change
Sample technologies162 164 -2 %-1 %642 663 -3 %-3 %
Diagnostic solutions196 180 +9 %+10 %749 698 +7 %+8 %
Of which QuantiFERON116 102 +13 %+14 %454 408 +11 %+11 %
Of which QIAstat-Dx32 26 +25 %+25 %109 88 +24 %+24 %
Of which NeuMoDx11 -19 %-19 %32 42 -24 %-24 %
Of which Other40 41 -2 %-2 %154 159 -3 %-2 %
PCR / Nucleic acid amplification82 81 +2 %+3 %300 300 %+1 %
Genomics / NGS66 65 +1 %+2 %234 239 -2 %-1 %
Other15 19 -24 %-21 %53 66 -19 %-15 %
Total net sales521 509 +2 %+3 %1,978 1,965 +1 %+1 %
Tables may have rounding differences. Percentage changes are to prior-year periods.

Sample technologies: Higher sales of consumables for use on QIAGEN instruments, as well as for Human ID / Forensics applications, led the performance in Q4 2024. The EZ2 Connect system reached a milestone of over 1,000 cumulative placements since launch. Overall sales were slightly lower than in Q4 2023 due to a modest sales decline in manual kits and challenging instrument sales trends that continued throughout 2024.

Diagnostic solutions: Q4 2024 sales grew 10% CER, and rose 12% CER excluding NeuMoDx, led by double-digit CER gains in consumables sales that absorbed a decline in instrument sales over Q4 2023. The QuantiFERON test for latent tuberculosis (TB) detection delivered 14% CER sales growth on solid demand in all regions as only about 40% of the global latent TB testing market has been converted to blood-based testing. QIAstat-Dx delivered 25% CER sales growth on double-digit gains in both consumables and instruments. The syndromic testing system surpassed the 2024 goal with over 660 new placements and reached more than 4,600 cumulative placements since launch. The NeuMoDx system remains on track for discontinuation in mid-2025.

PCR / Nucleic acid amplification: Q4 2024 sales rose 3% CER over the year-ago period driven by the QIAcuity digital PCR system, which saw double-digit CER growth in consumables and reached over 2,700 cumulative placements since launch despite ongoing challenging instrument purchasing trends. Sales of other PCR consumables grew at a low single-digit CER rate compared to Q4 2023.

Genomics / Next-generation sequencing (NGS): Sales for Q4 2024 grew 2% CER over Q4 2023, supported by growth in universal consumables used on third-party NGS systems. QIAGEN Digital Insights (QDI) sales increased at a single-digit CER rate, driven by growth in the clinical portfolio that more than offset a modest decline in the discovery portfolio. QDI's results in 2024 were adversely impacted by the ongoing transition to SaaS (software-as-a-service) subscription models, particularly in the pharmaceutical sector, from longer-term licensing agreements.

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Key cash flow data
In $ millionsQ4FY
20242023Change20242023Change
Net cash provided by operating activities192 151 +27 %674 459 +47 %
Purchases of property, plant and equipment(49)(52)-5 %(167)(150)+12 %
Free cash flow142 100 +43 %506 310 +63 %
Net cash used in investing activities(7)(59)NM(249)(88)NM
Net cash used in financing activities(489)(8)NM(423)(434)NM
Tables may have rounding differences. Percentage changes are to prior-year periods.

Net cash from operating activities was $674 million in 2024, a 47% increase from $459 million in 2023 that reflected reduced working capital requirements and a strong focus on cash flow optimization. Free cash flow rose 63% to $506 million in 2024, absorbing a slight increase in investments into property, plant and equipment.

As of December 31, 2024, cash, cash equivalents and short-term investments were $1.2 billion compared to $1.1 billion at the end of 2023. Key cash flow activities in 2024 included the repayment of $500 million in convertible notes that matured in November, net proceeds of $494.2 million from the issuance of new convertible notes in September, the return of approximately $300 million in January through a synthetic share repurchase and the repayment of $101.5 million of German private debt placements in June. The leverage ratio declined to 0.3x (net debt to adjusted EBITDA) as of December 31, 2024 compared to 0.6x at the end of 2023, but increased to 0.7x after completion of the approximately $300 million synthetic share repurchase in January 2025.

Portfolio update

QIAGEN is accelerating momentum in its Sample to Insight portfolio through targeted developments:

QIAstat-Dx: The QIAstat-Dx Gastrointestinal Panel Mini B&V (bacterial and viral) has received U.S. regulatory clearance, supporting outpatient diagnostics for gastrointestinal conditions. This panel detects five common bacterial and viral causes of gastrointestinal illnesses. A second version for outpatient use with five targets focused exclusively on bacterial infections is planned to soon be submitted for FDA clearance. Additionally, the QIAstat-Dx Rise system has also recently been submitted for FDA clearance, building on the launch of this higher-throughput system in Europe in 2022. These developments build on the FDA clearance of four QIAstat-Dx panels in 2024, enabling QIAGEN to offer a comprehensive menu of tests in the U.S. for diagnosis of respiratory, gastrointestinal and meningitis / encephalitis conditions.

QIAcuity digital PCR: This breakthrough system now supports multiplexing of up to 12 targets from a single sample, up from the previous limit of five. This enhancement, which requires no hardware changes, was enabled by the recent release of QIAcuity Software 3.1 and the new QIAcuity High Multiplex Probe PCR Kit. These innovations help provide deeper insights for translational research, microbiome analysis, pathogen detection as well as for novel cell and gene therapies.

Sample technologies: QIAGEN has surpassed a milestone of over 1,000 placements of the EZ2 Connect automated sample preparation instrument. This versatile platform supports kits to gain DNA and RNA from a wide range of sample types, opening up possibilities for downstream applications involving diagnostics, genomics and cancer as well as epidemiology and forensics.

Companion diagnostics: QIAGEN recently received FDA approvals for two new companion diagnostic tests to help guide treatment decisions, expanding the portfolio to 16 FDA-approved companion diagnostic tests based on the PCR technology.

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The therascreen KRAS RGQ PCR Kit was approved for use in identifying patients with metastatic colorectal cancer eligible for Amgen's Lumakras (sotorasib) in combination with Vectibix (panitumumab), and the therascreen BRAF V600E RGQ PCR Kit was approved for use with Array Biopharma’s Braftovi (encorafenib) in patients with metastatic melanoma.

QIAGEN Digital Insights (QDI): The QDI portfolio has been enhanced with new Artificial Intelligence features through a new AI extension for its Ingenuity Pathway Analysis (IPA). This software helps distill complex differential expression analyses into actionable insights. Additionally, QIAGEN is collaborating with Genomics England on the Generation Study, which aims to sequence the genomes of 100,000 newborns to screen for over 200 selected genetic conditions. The QIAGEN Clinical Knowledge Base contributes clinically relevant variant content for genes included in the point-of-care sequencing test, enabling rapid variant interpretation and reporting.

QIAGEN completes return of about $300 million to shareholders

In January 2025, QIAGEN completed the return of about $300 million to shareholders through a synthetic share repurchase. This follows a similar return of about $300 million at the start of 2024 as part of a commitment to return at least $1 billion to shareholders between 2024 and the end of 2028. This type of repurchase, which combines a direct capital repayment with a reverse stock split, offers a more efficient way to return cash to shareholders than an open-market repurchase while also enhancing earnings per share through a reduction in the number of shares outstanding.

Evolving the QIAGEN organization

As part of the QIAefficiency initiative launched in 2024 to simplify and improve operations, QIAGEN reorganized its global structure as of January 2025 by transforming its three Business Areas - Molecular Diagnostics, Life Sciences and QIAGEN Digital Insights - into two new global functional teams. The Product Portfolio & Innovation team, led by Nitin Sood, will integrate functions spanning Global Marketing, Clinical Medical Regulatory Affairs, R&D and Product Management. The Commercial Operations team, led by Fernando Beils, will unify and strengthen QIAGEN's sales and regional marketing teams. Both leaders will continue to serve on the Executive Committee.

Outlook

For 2025, QIAGEN has initiated an outlook that anticipates a continuation of the solid growth trends from H2 2024. Net sales are expected to rise about 4% CER (about 5% CER in the core business). Adjusted diluted EPS is expected to be at least $2.28 CER, supported by a goal to improve the adjusted operating income margin by at least 150 basis points to above 30% while absorbing lower non-operating income contributions and a higher adjusted tax rate than in 2024. For Q1 2025, net sales are expected to rise about 3% CER (about 4% CER in the core business) from $459 million in Q1 2024. Adjusted diluted EPS are expected to be at least $0.50 CER compared to $0.46 in Q1 2024.

Based on exchange rates as of February 1, 2025, for FY 2025, currency movements against the U.S. dollar are expected to have a negative impact on net sales of about two percentage points and a negative impact of about $0.02-$0.03 per share on adjusted EPS results. For Q1 2025, currency movements against the U.S. dollar are expected to have a negative impact on net sales of about two percentage points and a negative impact of about $0.01 per share on adjusted EPS results.

Investor presentation and conference call

A conference call is scheduled for Thursday, February 6, 2025, at 16:00 Frankfurt Time / 15:00 London Time / 10:00 New York Time. A live audio webcast will be accessible in the investor relations section of the QIAGEN website (www.qiagen.com), with a recording available after the event. The presentation will be published ahead of the call in this section: QIAGEN Investor Relations - Events and Presentations.
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Use of adjusted results

QIAGEN reports adjusted results, as well as results on a constant exchange rate (CER) basis, along with other non-U.S. GAAP (generally accepted accounting principles) measures, to provide deeper insights into its performance. These include metrics such as core sales (excluding discontinued products), adjusted gross margin, adjusted gross profit, adjusted operating income, adjusted operating expenses, adjusted operating income margin, adjusted net income, adjusted net income before taxes, adjusted diluted EPS, adjusted EBITDA, adjusted EPS, adjusted income taxes, adjusted tax rate, and free cash flow. Free cash flow is calculated by subtracting capital expenditures for property, plant and equipment from cash flow from operating activities. Adjusted results are non-GAAP financial measures that QIAGEN considers complementary to GAAP-reported results but not as substitutes. These measures exclude items that QIAGEN believes are outside of ongoing core operations, fluctuate significantly between periods, or hinder the comparability of results with competitors and prior periods. QIAGEN also uses non-GAAP and constant currency financial measures internally in planning, forecasting and reporting, and also for employee compensation. Additionally, adjusted results are used to compare current performance with historical results, which have consistently been presented on an adjusted basis.

About QIAGEN

QIAGEN N.V., a Netherlands-based holding company, is the leading global provider of Sample to Insight solutions, enabling customers to extract and gain valuable molecular insights from samples containing the building blocks of life. Our Sample technologies isolate and process DNA, RNA and proteins from blood, tissue and other materials. Assay technologies prepare these biomolecules for analysis while bioinformatics software and knowledge bases can be used to interpret data to find actionable insights. Automation solutions bring these processes together into seamless and cost-effective workflows. QIAGEN serves over 500,000 customers globally in Life Sciences (academia, pharma R&D and industrial applications, primarily forensics) and Molecular Diagnostics for clinical healthcare. As of December 31, 2024, QIAGEN employed more than 5,700 people in over 35 locations worldwide. For more information, visit www.qiagen.com.

Forward-Looking Statement

Certain statements in this press release may constitute forward-looking statements within the meaning of Section 27A of the U.S. Securities Act of 1933, as amended, and Section 21E of the U.S. Securities Exchange Act of 1934, as amended. These statements, including those regarding QIAGEN's products, development timelines, marketing and / or regulatory approvals, financial and operational outlook, growth strategies, collaborations and operating results - such as expected adjusted net sales and adjusted diluted earnings - are based on current expectations and assumptions. However, they involve uncertainties and risks. These risks include, but are not limited to, challenges in managing growth and international operations (including the effects of currency fluctuations, regulatory processes and logistical dependencies), variability in operating results and allocations between customer classes, commercial development for our products to customers in the Life Sciences and clinical healthcare, changes in relationships with customers, suppliers or strategic partners; competition and rapid technological advancements; fluctuating demand for QIAGEN's products due to factors such as economic conditions, customer budgets and funding cycles; obtaining and maintaining regulatory approvals for our products; difficulties in successfully adapting QIAGEN's products into integrated solutions and producing these products; and protecting product differentiation from competitors. Additional uncertainties may arise from market acceptance of new products, integration of acquisitions, governmental actions, global or regional economic developments, natural disasters, political or public health crises, and other "force majeure" events. There is also no guarantee that anticipated benefits from acquisitions will materialize as expected. For a comprehensive overview of risks, please refer to the “Risk Factors” contained in our most recent Annual Report on Form 20-F and other reports filed with or furnished to the U.S. Securities and Exchange Commission.




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Contacts

Investor Relations
Public Relations
John Gilardi
+49 152 018 11711
Thomas Theuringer
+49 2103 29 11826
Domenica Martorana
+49 152 018 11244Lisa Specht+49 2013 29 14181
e-mail: ir@QIAGEN.com
e-mail: pr@QIAGEN.com

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QIAGEN N.V.
CONDENSED CONSOLIDATED STATEMENTS OF INCOME
(unaudited)
(In $ thousands, except per share data)Three monthsTwelve months
ended December 31,ended December 31,
2024202320242023
Net sales$521,202 $509,162 $1,978,214 $1,965,311 
Cost of sales:
Cost of sales174,401 177,018 952,323 667,425 
Acquisition-related intangible amortization13,511 16,044 58,541 64,198 
Total cost of sales187,912 193,062 1,010,864 731,623 
Gross profit333,290 316,100 967,350 1,233,688 
Operating expenses:
Sales and marketing113,860 117,478 450,929 459,912 
Research and development48,605 45,966 193,494 198,511 
General and administrative27,852 28,474 113,432 119,254 
Acquisition-related intangible amortization1,809 2,692 9,596 10,764 
Restructuring, acquisition, integration and other, net22,066 10,875 102,188 35,309 
Total operating expenses214,192 205,485 869,639 823,750 
Income from operations119,098 110,615 97,711 409,938 
Other income (expense):
Interest income15,092 19,261 68,016 78,992 
Interest expense(11,143)(12,441)(43,841)(53,410)
Other income (expense), net2,805 1,441 (739)(5,711)
Total other income, net6,754 8,261 23,436 19,871 
Income before income tax expense125,852 118,876 121,147 429,809 
Income tax expense37,530 21,212 37,556 88,506 
Net income$88,322 $97,664 $83,591 $341,303 
Diluted earnings per common share$0.39 $0.42 $0.37 $1.48 
Diluted earnings per common share (adjusted)$0.61 $0.55 $2.18 $2.07 
Diluted shares used in computing diluted earnings per common share224,245 230,745 224,717 230,619 


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QIAGEN N.V.
RECONCILIATION OF REPORTED TO ADJUSTED RESULTS
(In $ millions, except EPS data)
(unaudited)

Three months ended December 31, 2024
Net
Sales
Gross
Profit
Operating
Income
Pre-tax
Income
Income
Tax
Tax
Rate
Net
Income
Diluted EPS*
Reported results521.2 333.2 119.1 125.8 (37.5)30 %88.3 $0.39 
Adjustments:
Business integration, acquisition and restructuring related items (a)— 3.0 25.1 25.1 (4.6)20.5 0.09 
Purchased intangibles amortization
— 13.5 15.3 15.3 (3.8)11.5 0.05 
Non-cash interest expense charges (b)
— — — 2.4 — 2.4 0.01 
Non-cash other income, net (c)
— — — 0.5 — 0.5 0.00 
Certain income tax items (d)
— — — — 13.2 13.2 0.06 
Total adjustments— 16.6 40.3 43.3 4.8 48.1 0.22 
Adjusted results521.2 349.8 159.4 169.1 (32.7)19 %136.4 $0.61 
*Using 224.2 M diluted shares    


Twelve months ended December 31, 2024
Net
Sales
Gross
Profit
Operating
Income
Pre-tax
Income
Income
Tax
Tax
Rate
Net
Income
Diluted EPS*
Reported results1,978.2 967.3 97.7 121.1 (37.5)31 %83.6 $0.37 
Adjustments:
Business integration, acquisition and restructuring related items (a)— 298.9 401.1 401.1 (78.6)322.5 1.44 
Purchased intangibles amortization
— 58.5 68.1 68.1 (16.8)51.3 0.23 
Non-cash interest expense charges (b)
— — — 17.0 — 17.0 0.08 
Non-cash other income, net (c)
— — — 3.1 — 3.1 0.01 
Certain income tax items (d)
— — — — 13.2 13.2 0.06 
Total adjustments— 357.5 469.3 489.4 (82.2)407.2 1.81 
Adjusted results1,978.2 1,324.8 567.0 610.5 (119.7)20 %490.8 $2.18 
*Using 224.7 M diluted shares

(a) Includes costs incurred in connection with streamlining operations and improving overall efficiency as well as costs related to various contemplated and completed acquisition projects and their subsequent integration.
(b) Cash Convertible Notes were recorded at an original issue discount that is recognized as incremental non-cash interest expense over the expected life of the notes.
(c) Adjustment includes the net impact of changes in fair value of the Call Options and the Embedded Cash Conversion Options related to the Cash Convertible Notes.
(d) These items represent updates in QIAGEN's assessment of ongoing examinations or other tax items that are not indicative of the Company's normal future income tax expense.

Tables may contain rounding differences.
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QIAGEN N.V.
CONDENSED CONSOLIDATED BALANCE SHEETS

(In $ thousands, except par value)December 31, 2024December 31, 2023
Assets(unaudited)
Current assets:
Cash and cash equivalents$663,555 $668,084 
Short-term investments489,437 389,698 
Accounts receivable, net349,278 381,877 
Inventories, net279,256 398,385 
Prepaid expenses and other current assets178,327 309,516 
Total current assets1,959,853 2,147,560 
Long-term assets:
Property, plant and equipment, net753,611 765,037 
Goodwill2,425,418 2,475,732 
Intangible assets, net303,815 526,821 
Other long-term assets246,925 200,040 
Total long-term assets3,729,769 3,967,630 
Total assets$5,689,622 $6,115,190 
Liabilities and equity
Current liabilities:
Current portion of long-term debt$53,481 $587,970 
Accrued and other current liabilities406,876 407,168 
Accounts payable83,272 84,155 
Total current liabilities543,629 1,079,293 
Long-term liabilities:
Long-term debt, net of current portion1,338,067 921,824 
Other long-term liabilities240,587 306,309 
Total long-term liabilities1,578,654 1,228,133 
Equity:
Common shares, 0.01 EUR par value, authorized—410,000 shares, issued—223,904 and 230,829 shares, respectively
2,601 2,702 
Additional paid-in capital1,666,070 1,915,115 
Retained earnings2,448,122 2,456,800 
Accumulated other comprehensive loss(474,539)(433,830)
Less treasury stock, at cost — 1,614 and 2,627 shares, respectively
(74,915)(133,023)
Total equity3,567,339 3,807,764 
Total liabilities and equity$5,689,622 $6,115,190 

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QIAGEN N.V.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS


(In $ thousands)Twelve Months Ended December 31,
20242023
Cash flows from operating activities:(unaudited)
Net income$83,591 $341,303 
Adjustments to reconcile net income to net cash provided by operating activities, net of effects of businesses acquired:
Depreciation and amortization203,268 205,336 
Non-cash impairments203,408 4,158 
Amortization of debt discount and issuance costs18,428 30,162 
Share-based compensation expense43,627 47,100 
Deferred tax (benefit) expense(23,041)10,731 
Other items, net including fair value changes in derivatives8,817 7,623 
Change in operating assets, net113,013 (94,825)
Change in operating liabilities, net22,440 (92,133)
Net cash provided by operating activities673,551 459,455 
Cash flows from investing activities:
Purchases of property, plant and equipment(167,174)(149,710)
Purchases of intangible assets(4,068)(13,092)
Purchases of short-term investments(685,915)(976,448)
Proceeds from redemptions of short-term investments584,979 1,270,551 
Cash paid for acquisitions, net of cash acquired— (149,532)
Cash received (paid) for collateral asset25,414 (66,583)
Purchases of investments, net(2,465)(2,870)
Other investing activities— 29 
Net cash used in investing activities(249,229)(87,655)
Cash flows from financing activities:
Proceeds from long-term debt, net of issuance costs494,211 — 
Repayment of long-term debt(601,536)(400,000)
Capital repayment(292,099)— 
Proceeds from exercise of call options related to cash convertible notes— 36,762 
Payment of intrinsic value of cash convertible notes— (36,762)
Tax withholding related to vesting of stock awards(34,160)(17,675)
Cash received (paid) for collateral liability11,350 (16,315)
Other financing activities(662)163 
Net cash used in financing activities(422,896)(433,827)
Effect of exchange rate changes on cash and cash equivalents(5,955)(558)
Net decrease in cash and cash equivalents(4,529)(62,585)
Cash and cash equivalents, beginning of period668,084 730,669 
Cash and cash equivalents, end of period$663,555 $668,084 
Reconciliation of free cash flow(1)
Net cash provided by operating activities$673,551 $459,455 
Purchases of property, plant and equipment(167,174)(149,710)
Free cash flow$506,377 $309,745 
(1) Free cash flow is a non-GAAP financial measure and is calculated from net cash provided by operating activities reduced by purchases of property, plant and equipment.
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