Lonza Group AG Overview
Lonza is the world's largest and longest-established pure-play contract development and manufacturing organization (CDMO). It sells development, manufacturing and technology services to pharmaceutical and biotechnology companies across the main modalities:
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mammalian and microbial biologics;
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small-molecule APIs and drug products;
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antibody-drug conjugates (ADCs) and bioconjugates;
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cell and gene therapies;
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mRNA.
Following the March 2026 agreement to sell Capsules & Health Ingredients (CHI) to Lone Star Funds, Lonza is completing a two-year transformation into a focused CDMO. It now operates three business platforms: Integrated Biologics, Advanced Synthesis and Specialized Modalities. Its differentiation rests on four things:
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scale, including Visp, Vacaville (the largest US biologics CDMO site) and Portsmouth;
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an integrated drug-substance-to-drug-product offering;
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a proprietary toolbox: GS Xceed® expression, Ibex®, Synaffix® ADC linkers and the Nona TfR1 BBB technology;
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a quality track record across 125+ years of chemical and biological manufacturing.
FY2025 continuing sales were CHF 6.5bn at a 31.6% CORE EBITDA margin. Management guides FY2026 to 11–12% CER growth and a 33–34% margin.
Company's own description. In its 2026 releases Lonza calls itself the world's leading CDMO "dedicated to serving the healthcare industry." It describes a team of around 20,000 people working with pharma and biotech customers to turn breakthrough innovations into viable therapies, using science, smart technology and lean manufacturing (H1 2026 release boilerplate). The FY2025 FYR and AR2025 present the business as three complementary, integrated CDMO Business Platforms "powered by the Lonza Engine®." The Lonza Engine is the company's term for its combined strengths in science, smart technology and lean manufacturing for complex and emerging modalities (6 Mar 2026 release).
What Lonza does. Lonza takes a customer's molecule, from DNA sequence or chemical route, and develops and manufactures it. Work runs from pre-clinical development through clinical supply to commercial launch and lifecycle manufacturing. Revenue comes from four sources:
Development services: Cell-line development, process and analytical development, formulation and regulatory CMC. Typically billed fee-for-service or per milestone.
Clinical and commercial manufacturing: Drug substance and drug product. Usually batch-based or capacity-reservation contracts, often with take-or-pay or minimum-volume features. Large commercial deals are frequently multi-year and sometimes involve customer co-funding of dedicated capacity, as in the Ibex model and the 2026 Stein ADC line backed by a long-term customer commitment.
Technology licensing: GS Xceed® expression system licences, Synaffix ADC technology licences with upfront/milestone/royalty structures, bYlok® and the Nona TfR1 BBB platform.
Products (Bioscience): Cell-culture media, primary cells, transfection systems (Nucleofector™), endotoxin and microbial testing. Sold as consumables and instruments.
Revenue-model mix. Lonza does not publish an exact split between product, service, subscription and licensing revenue. The analyst estimate is that more than 90% of continuing revenue is service-based CDMO revenue (development plus manufacturing). The rest is Bioscience products, reported within Specialized Modalities, and technology licensing. There is no subscription revenue. Licensing is strategically important as a customer-acquisition funnel but financially small; its amount is not separately disclosed.
Value-chain position. Lonza sits between drug innovators (big pharma, mid-cap and small biotech) and patients. It is an outsourced manufacturer that carries large fixed-asset intensity:
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PP&E of CHF 8.3bn at FY2025 (S&P/StockAnalysis);
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CapEx of CHF 1.3bn in FY2025, 19.6% of sales (FY2025 FYR).
Its upstream suppliers are equipment, single-use consumable, raw-material and media vendors. Downstream, its customers own the regulatory licences and commercialize the drugs.
Customer types:
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Large pharmaceutical companies outsourcing commercial capacity. Examples are the strategic multi-site US biopharma collaboration expanded on 1 Jul 2026 and the Vacaville commercial contracts.
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Mid-size and emerging biotech needing integrated DNA-to-IND and clinical supply. Example: the ImmuneOncia late-stage mAb deal, March 2026.
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Academic and research customers (Bioscience).
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Cell and gene therapy developers (autologous and allogeneic).
End-markets. The main end-markets are:
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biologic therapeutics (mAbs, bispecifics, fusion proteins);
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ADCs and bioconjugates in oncology;
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small-molecule APIs including highly potent APIs (HPAPI);
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cell and gene therapy;
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microbial-derived proteins, peptides and enzymes;
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mRNA/LNP;
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research tools.
Analyst characterization. Lonza is a capital-heavy, scale-advantaged infrastructure provider to biopharma. Its economics depend on asset utilization:
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New plants dilute margins during ramp-up. This was visible in FY2023, when the CORE EBITDA margin fell to 29.8%, and in early Vacaville.
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Mature, full assets earn returns well above group average. Advanced Synthesis reached a 48.1% CORE EBITDA margin in H1 2026.
The CHI exit removes a lower-growth consumer-health and capsule business that lacked CDMO synergy. It turns Lonza into a purer "picks-and-shovels" exposure to biologic and complex-modality pipelines. The key debates are:
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the pace of capacity absorption at Vacaville and Visp large-scale;
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competitive intensity from Asian CDMOs and big-pharma insourcing;
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capital intensity versus free-cash-flow conversion.
Strategy
Stated strategy: "One Lonza." The latest annual report and releases set out four themes:
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Become the world-leading pure-play CDMO by exiting non-CDMO and less attractive CDMO offerings. Delivered: CHI, Cocoon, MODA and Monteggio, described as four divestments in under two years.
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Operate through three complementary, integrated Business Platforms powered by the Lonza Engine® (science, smart technology, lean manufacturing).
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Strengthen customer centricity through a group-wide Strategic Enterprise Account Management team. Lonza reports a significant uplift in an already industry-leading net promoter score (FY2025 FYR).
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Drive operational and quality excellence through cross-platform Group Operations and Quality functions, manufacturing productivity, and disciplined CapEx execution.
A newly formed corporate strategy, innovation and M&A team focuses on value creation as a pure-play CDMO, through organic growth and bolt-on acquisitions across current and future Technology Platforms (FY2025 FYR).
CDMO Organic Growth Model (medium-term framework):
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low-teens organic CER sales growth on average over time;
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CORE EBITDA growing faster than sales;
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CapEx intensity in the mid-to-high-teens percent of sales (FY2025 FYR footnote; H1 2026 release).
Capital allocation framework. CHI upfront proceeds (CHF 1.7bn+) go to a discretionary cash pool to fund prioritized organic growth and bolt-on M&A. CHF 500m will be returned through an expedited share buyback after closing (6 Mar 2026 investor presentation; H1 2026 release). Dividend policy is progressive: +25% to CHF 5.00 for FY2025, with 50% paid from capital-contribution reserves free of Swiss withholding tax.
Guidance (latest):
Lonza's earlier mid-term ambitions (from 2023–2024 investor communications) referenced CORE EBITDA margins in the low-to-mid 30s.
Products & Services
Pricing is not publicly disclosed for any CDMO service. Commercial terms are negotiated per contract (batch pricing, capacity reservation, milestone or royalty for technology licences). Sources: lonza.com offering navigation (accessed Oct 2026); Lonza news releases 2023–2026.
Integrated Biologics
| Offering | Description / capabilities | Target customer | Notes / flagship |
|---|---|---|---|
| GS Xceed® Gene Expression System | CHO glutamine-synthetase expression system with high-titre cell lines; licensed widely, including within approved drugs | Biotech and pharma developing mAbs and recombinant proteins | Flagship licensing franchise; licence plus royalty model (terms not disclosed) |
| GS piggyBac® Transposon Technology | Transposon-based integration for faster, higher-expressing cell lines | Biologics developers | Add-on to GS platform |
| GS Effex® Cell Line | Afucosylated-antibody CHO host for enhanced ADCC | Oncology/immunology mAb developers | Specialty host |
| GS Discovery® Transient Expression | Transient expression for early material | Discovery-stage biotech | Early de-risking |
| bYlok® Bispecific Pairing Technology | Engineering technology to drive correct heavy/light-chain pairing in bispecifics | Bispecific developers | Differentiator for complex formats |
| XS Technologies® Platform | Integrated cell-line, process and media platform for expression | Biologics developers | Platform bundle |
| Early De-risking & Optimization | Developability, manufacturability, formulatability and immunogenicity/immunotoxicity (in silico and in vitro) assessments; early protein expression | Pre-IND biotech | Funnel into DNA-to-IND |
| Integrated DNA-to-IND Programs | End-to-end packages for mAbs, bispecifics, Fab fragments, Fc-fusion proteins, scaffolds and other recombinant proteins | Emerging biotech | Enhanced offering announced 8 Jul 2026 (acceleration, de-risking) |
| Development Services | Biologics process development, analytical development, formulation and primary-packaging development | All biologics customers | Basel, Slough, Portsmouth, Singapore |
| Mammalian Drug Substance Manufacturing | Clinical to commercial scale, from small/mid-scale to 20,000L-class stainless steel (Vacaville, Visp large-scale, Portsmouth, Singapore, Porriño) | Big pharma and late-stage biotech | Vacaville (acquired 2024) is "one of the world's largest biologics facilities" at ~956,000 sq ft (Pharma Manufacturing, Mar 2026); five significant commercial contracts signed. Visp large-scale started commercial operations in H1 2026. |
| OptiALTO® Intensified Fed-Batch Platform | Process-intensification platform to raise volumetric productivity | Commercial programs | N-1 perfusion and intensification is part of the expanded US biopharma collaboration (Jul 2026) |
| Drug Product Manufacture / Services | Aseptic fill-finish of vials and syringes; clinical DP in Basel/Stein; large-scale commercial DP facility under construction in Stein (operations now expected 2028, scope expanded to high-value small-molecule DP) | Integrated DS–DP customers | ~USD 514m Stein investment originally announced (Pharmaceutical Commerce) |
| Tailored License Application Program; Cell Line Development | Licensing and contract cell-line development | Biologics developers | — |
| Biologics Regulatory Affairs | CMC regulatory support | All customers | — |
| TfR1 Blood-Brain-Barrier Technology (from Nona Biosciences) | TfR1-binding single-domain VHH shuttle, usable as an IgG fusion or via GlycoConnect® conjugation | CNS therapy developers | Rights acquired 2 Jul 2026; preclinical data show improved brain delivery versus an industry benchmark in a transgenic model |
Advanced Synthesis
| Offering | Description / capabilities | Target customer | Notes / flagship |
|---|---|---|---|
| Drug Substance / API Services | Early-phase through commercial API development and manufacturing | Small-molecule developers | Visp, Nansha (CN) and others |
| Design2Optimize® | Model-based process development using DoE and simulation to cut development time | Early/late-phase small molecules | Proprietary method |
| AI-Enabled Route Scouting Service | Computational retrosynthesis and route selection | Discovery/early development | Digital differentiation |
| High-Throughput Experimentation; PBPK Modeling; Solid Form Services; Pharmaceutical Method Development | Supporting development science | Small-molecule developers | — |
| Highly Potent API (HPAPI) Technologies | Handling, development and manufacturing at low and high potency | Oncology small molecules, ADC payloads | Visp payload-linker expansion announced 30 Jun 2026, operational 2028 (BioAlps) |
| Bioavailability Enhancement | Amorphous solid dispersion, spray-dried dispersion, hot-melt extrusion | Poorly soluble molecules | Bend, Oregon is the historic centre of excellence |
| Oral Drug Product | Clinical trial material, formulation, preformulation, process optimization, inhalation (dry-powder) development, integrated offerings | Small-molecule developers | — |
| Regulatory Affairs CMC Services | CMC development and submissions | All | — |
| Bioconjugation Services | Early development, ADC drug-substance manufacturing, analytical services, targeting agent and carrier protein, process development, clinical and commercial ADC manufacturing, payload development | ADC developers | Visp bioconjugate suites (expansion with two suites announced Nov 2024) |
| Ibex® Design ADC DNA-to-IND Program | Integrated ADC development package | Emerging ADC biotech | Built on Ibex® Visp campus |
| ADC Technologies Platform (Synaffix) | GlycoConnect® site-specific conjugation, HydraSpace® polar spacer, toxSYN® payload-linker platform; licensing model with upfront, milestone and royalty | ADC innovators | Acquired 2023; new licensing deals continue (2026) |
| Commercial-scale aseptic ADC Drug Product (Stein) | Dedicated commercial ADC fill-finish under construction, plus an additional multipurpose ADC filling line announced 22 Jul 2026 (operational 2030), backed by a long-term big-pharma collaboration | Commercial ADC customers | End-to-end ADC chain: mAb (Visp) → payload-linker (Visp) → conjugation (Visp) → DP (Stein) |
Specialized Modalities
| Offering | Description / capabilities | Target customer | Notes / flagship |
|---|---|---|---|
| Cell & Gene: process development and cGMP manufacturing | Autologous and allogeneic cell therapies, viral vectors (AAV/LV), exosomes | CGT developers | Portsmouth NH, Houston TX, Geleen NL. A sixth commercial therapy was approved on the C&G platform in H1 2026. |
| Cocoon® Platform (Personalized Medicines) | Automated closed-system autologous manufacturing | Point-of-care CGT | Agreed for divestment to Octane Medical Group (disclosed 6 Mar 2026) |
| Microbial | Strain development, process development, drug-substance manufacturing, analytics (proteins, peptides, enzymes, plasmid DNA) | Biotech and pharma | Visp, Kouřim (CZ). Strong H1 2026 growth after a customer-related plant adaptation. |
| mRNA/LNP | Process development, analytics, mRNA manufacturing, lipid-nanoparticle encapsulation | Vaccine and therapeutic mRNA developers | Legacy of the Moderna collaboration; partnership with Ethris on intranasal spray-dried mRNA vaccines (2026) |
| Bioscience Products | Primary cells and media, Nucleofector™ transfection (Amaxa), cell-culture media, endotoxin/pyrogen and rapid microbial testing, QC software | Research labs, QC labs, manufacturers | Robust CER growth throughout 2025 and H1 2026 |
| MODA® software platform | QC/manufacturing data and quality-execution software | Pharma QC | Agreed for divestment to the parent of STARLIMS (disclosed 6 Mar 2026) |
Discontinued: Capsules & Health Ingredients (pending sale to Lone Star)
| Offering | Description | Status |
|---|---|---|
| Capsugel® hard capsules | Gelatin and plant-based (HPMC/pullulan) hard empty capsules for pharma and nutraceutical | Divestment to Lone Star; Lonza retains 40% |
| Health Ingredients | Branded nutritional ingredients | Same |
| Dosage-form solutions | Encapsulation and formulation services | Same |
| FY2025 / H1 2026 metrics | FY2025 CER growth +3.9%; CORE EBITDA margin 25.9% (24.7% as discontinued-operation basis). H1 2026 sales CHF 541m (+6.3% CER), margin 26.8%. | FY2025 FYR; H1 2026 release |
Financial Narrative
Basis. FY2021–FY2023 are group figures including CHI (excluding LSI). FY2024–FY2025 are continuing operations excluding CHI for P&L lines. Balance-sheet lines are group-level (FY2025 CHI assets are in held-for-sale). The data comes from S&P/StockAnalysis standardized statements, Lonza FYR and AR financial highlights, and the FY2025 APM report.
Income statement
Notes on the income statement:
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FY2024 –18.4% AER is the CHI perimeter break. The FY2024 CER +1.3% is the continuing-basis growth (FY2025 FYR).
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FY2022 and FY2023 IFRS EBITDA are derived from reported EBITDA margins of 34.4% and 28.9% (Lonza AR2023 financial highlights).
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FY2021 net income includes the LSI disposal gain.
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FY2025 net income is a group loss. Continuing operations earned CHF 909m (+51% YoY). Discontinued operations lost CHF 1,184m, mainly a CHF 1,229m goodwill impairment on CHI (AR2025 consolidated statements).
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Company-defined EBIT (continuing) was CHF 908m in FY2024 and CHF 1,239m in FY2025 (FY2025 FYR). S&P's standardized operating income differs because of classification of certain items.
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CORE EPS (continuing) was CHF 15.08 basic / 15.03 diluted in FY2025, versus CHF 13.12 / 13.10 in FY2024 (Lonza FY2025 FYR). H1 2026 EPS was CHF 8.14 versus CHF 5.65 in H1 2025 (Simply Wall St summary of H1 2026 report).
Margins (%)
Revenue CAGR. FY2021–FY2025 reported revenue CAGR is ~4.8% (derived; distorted by the CHI exit). On a like-for-like CDMO basis, CER growth averaged in the mid-teens over 2021–2025. Detail: 20% (2021), 15.1% (2022), 10.9% (2023, group), 1.3% (2024, continuing), 21.7% (2025, continuing; low-teens organic ex-Vacaville).
Commentary. Profitability peaked in 2022 at a 32.1% CORE EBITDA margin. That year combined COVID mRNA volumes with high utilization. 2023 was the trough (29.8%, guided down twice): mRNA volumes rolled off, Moderna terminated, biotech funding was tight, capsule demand was weak, and large new assets started depreciating and ramping.
Since 2024 the continuing CDMO business has re-expanded margins steadily: 30.2% (FY2024), 31.6% (FY2025), 34.8% (H1 2026), and guidance of 33–34% for FY2026. The drivers are maturing growth projects, Advanced Synthesis mix and operating leverage, partly offset by Vacaville dilution.
The gap between IFRS and CORE EBITDA narrowed in FY2025: CHF 1,970m versus CHF 2,064m, a 1.4-ppt gap versus 3.7 ppts in FY2024. This reflects lower restructuring and divestiture charges, although one-off environmental and impairment costs persisted.
Balance sheet
Notes on the balance sheet. Short-term debt is the S&P short-term debt plus current portion of LTD, excluding leases. Lonza's own net-debt definition (AR2025 financial highlights) shows net cash in 2021–2022.
FY2025 goodwill and intangibles fell because CHI assets were reclassified to held-for-sale and goodwill was impaired. "Other current assets" of CHF 2,795m at FY2025 are mostly CHI assets held for sale. This also inflates FY2025 working capital.
H1 2026 balance sheet (30 Jun 2026, S&P): cash CHF 487m; total debt CHF 4,167m; equity CHF 8,152m; total assets CHF 18,258m.
Cash flow
Dividends paid are an analyst estimate: prior-year DPS multiplied by approximate shares outstanding. They are not company-reported cash-flow lines.
Lonza-defined cash metrics (FY2025 FYR):
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Operational free cash flow before acquisitions and divestitures, group: CHF 674m in FY2025 (+42.5%) versus CHF 473m in FY2024.
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CDMO free cash flow: CHF 545m in FY2025 versus CHF 313m, "nearly doubled."
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CapEx intensity: 30% of sales in 2022; 25% in 2023; 19.6% in 2025; 15.7% in H1 2026.
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H1 2026 FCF: CHF 0.4bn (+CHF 0.3bn YoY).
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S&P TTM to Jun 2026: OCF CHF 1,435m, CapEx CHF 1,228m, FCF CHF 207m.
Ratios
Notes on the ratios:
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ROE and ROA are derived from net income and year-end balances.
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The FY2024 and FY2025 net debt/CORE EBITDA ratios conflict between sources. The FY2025 FYR reports 1.4x (FY2025) and 1.5x (FY2024). The AR2025 historical table shows 1.6x and 1.7x. The difference is the perimeter of CORE EBITDA (continuing versus total group including CHI).
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The FY2024 cash conversion cycle and asset turnover are distorted: the P&L is restated to exclude CHI while the balance sheet still includes CHI.
Trend commentary. The defining financial feature of the period is a deliberate leveraging-up to fund capacity. Lonza went from CHF 958m net cash (2021, post-LSI) to CHF 3.26bn net debt (2025). The drivers were roughly CHF 7.5bn of cumulative CapEx over 2021–2025, the USD 1.2bn Vacaville acquisition, and about CHF 2.5bn of buybacks over 2021–2025 (net repurchases per S&P).
Returns compressed as the asset base grew faster than earnings: PP&E rose 77% from 2021 to 2025. They are now inflecting:
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CapEx intensity is normalizing toward the mid-to-high-teens range of the CDMO Organic Growth Model.
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The FY2026 CORE EBITDA margin is guided at 33–34%.
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The CHI proceeds (CHF 1.7bn upfront) should take leverage "well below" the target range (6 Mar 2026 release).
The FY2025 statutory loss is purely a non-cash CHI write-down and does not reflect continuing-business economics.
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View Subscription PlansFinancial Detail
Business Platform Details
| Business Platform | Contents | Head |
|---|---|---|
Integrated Biologics (IB) | Mammalian drug substance (clinical and commercial, all scales: Visp, Portsmouth, Vacaville, Slough, Singapore, Porriño and others), biologics drug product (Basel, Stein), expression technologies (GS Xceed®, GS piggyBac®, GS Effex®, bYlok®, XS Technologies®), early de-risking, DNA-to-IND programs | Gordon Bates |
Advanced Synthesis (AS) | Small molecules (API/drug substance, HPAPI, bioavailability enhancement, oral drug product; Visp, Bend OR, Nansha/Guangzhou and others), bioconjugates/ADCs (Visp incl. Ibex, conjugation suites), Synaffix ADC technology platform, payload-linkers | Christian Seufert |
Specialized Modalities (SM) | Cell & Gene (Portsmouth, Houston/Pearland, Geleen), Microbial (Visp, Kouřim), mRNA/LNP, Bioscience products (research media, cells, Nucleofector™, testing) | Daniel Palmacci |
Corporate | Group functions, central hedging program (FY2025 hedging impact on sales CHF 71m, CORE EBITDA CHF 35m), residual activities | — |
Discontinued: CHI | Capsugel hard capsules, health ingredients, dosage-form solutions; held for sale pending close with Lone Star | Jean-Christophe Hyvert |
Revenue by Segment
| Segment (sales, CHF Mn) | FY2024 | FY2025 |
|---|---|---|
Integrated Biologics | 2,883 | 3,649 |
Advanced Synthesis | 1,323 | 1,611 |
Specialized Modalities | 1,099 | 1,034 |
Corporate | 175 | 237 |
Total continuing sales | 5,480 | 6,531 |
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View Subscription PlansRevenue by Segment — Integrated Biologics
| Segment (CORE EBITDA, CHF Mn) | FY2024 | FY2025 |
|---|---|---|
Integrated Biologics | 1,045 | 1,287 |
Advanced Synthesis | 484 | 674 |
Specialized Modalities | 192 | 176 |
Corporate | -68 | -73 |
Total CORE EBITDA | 1,653 | 2,064 |
Segment CORE EBITDA margin (%)
| Segment CORE EBITDA margin (%) | FY2024 | FY2025 |
|---|---|---|
Integrated Biologics | 36.2 | 35.3 |
Advanced Synthesis | 36.6 | 41.8 |
Specialized Modalities | 17.5 | 17.0 |
Group | 30.2 | 31.6 |
Segment growth and mix (%)
| Segment growth and mix (%) | FY2024 | FY2025 |
|---|---|---|
IB CER growth | 0 | 32.2 |
AS CER growth | 0 | 22.4 |
SM CER growth | 0 | -3.0 |
IB share of total sales | 52.6 | 55.9 |
AS share of total sales | 24.1 | 24.7 |
SM share of total sales | 20.1 | 15.8 |
Segment Revenue
| Platform | H1 2026 CER growth | H1 2026 CORE EBITDA margin | Change vs H1 2025 |
|---|---|---|---|
Integrated Biologics | +10.0% | 36.0% | flat |
Advanced Synthesis | +27.7% | 48.1% | +6.8 ppts |
Specialized Modalities | +22.6% | 28.0% | +10.7 ppts |
Group (continuing) | +16.0% (+11.2% AER) | 34.8% | +4.4 ppts |
Group continuing (CHF Mn) | H1 2025 | H1 2026 | — |
Sales | 3,034 | 3,374 | — |
CORE EBITDA | 922 | 1,175 | — |
EBITDA | 877 | 1,152 | — |
EBIT | 573 | 789 | — |
Revenue by Segment (FY2021–FY2023)
| Division (sales, CHF Mn) | FY2021 | FY2022 | FY2023 |
|---|---|---|---|
Biologics | 2,699 | 3,274 | 3,719 |
Small Molecules | 767 | 819 | 901 |
Cell & Gene | 602 | 693 | 696 |
Capsules & Health Ingredients (derived) | 1,204 | 1,266 | 1,161 |
Corporate | 137 | 171 | 240 |
Total group sales | 5,409 | 6,223 | 6,717 |
Revenue by Segment by Division
| Division (CORE EBITDA, CHF Mn) | FY2021 | FY2022 | FY2023 |
|---|---|---|---|
Biologics | 979 | 1,228 | 1,294 |
Small Molecules | 215 | 248 | 283 |
Cell & Gene | 106 | 116 | 64 |
Capsules & Health Ingredients | 414 | 418 | 327 |
Corporate (derived) | -49 | -15 | 31 |
Total group CORE EBITDA | 1,665 | 1,995 | 1,999 |
Division CORE EBITDA margin (%)
| Division CORE EBITDA margin (%) | FY2021 | FY2022 | FY2023 |
|---|---|---|---|
Biologics | 36.3 | 37.5 | 34.8 |
Small Molecules | 28.0 | 30.3 | 31.4 |
Cell & Gene | 17.6 | 16.7 | 9.2 |
Capsules & Health Ingredients | 34.4 | 33.0 | 28.2 |
Income Statement and Margin Analysis (%)
| Metric | FY2021 | FY2022 | FY2023 | FY2024 | FY2025 |
|---|---|---|---|---|---|
Revenue (CHF Mn) | 5,409 | 6,223 | 6,717 | 5,480 | 6,531 |
Revenue growth AER (%) | 20.0 | 15.1 | 7.9 | -18.4 | 19.2 |
Revenue growth CER (%) | 20.0 | 15.1 | 10.9 | 1.3 | 21.7 |
Gross profit (CHF Mn) | 2,110 | 2,438 | 2,403 | 2,006 | 2,349 |
Operating income, S&P standardized (CHF Mn) | 846 | 1,387 | 1,365 | 1,110 | 1,397 |
EBITDA, IFRS reported (CHF Mn) | 1,365 | 2,141 | 1,941 | 1,452 | 1,970 |
CORE EBITDA (CHF Mn) | 1,665 | 1,995 | 1,999 | 1,653 | 2,064 |
Pre-tax income (CHF Mn, derived from S&P pretax margin) | 760 | 1,448 | 790 | 708 | 1,101 |
Net income attributable (CHF Mn) | 2,944 | 1,215 | 654 | 636 | -275 |
EPS basic, reported (CHF) | 39.52 | 16.34 | 8.88 | 8.92 | -3.93 |
Dividend per share for the fiscal year (CHF) | 3.00 | 3.50 | 4.00 | 4.00 | 5.00 |
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View Subscription PlansMargin Analysis (%)
| Metric | FY2021 | FY2022 | FY2023 | FY2024 | FY2025 |
|---|---|---|---|---|---|
Gross margin (%) | 39.0 | 39.2 | 35.8 | 36.6 | 36.0 |
Operating margin, S&P (%) | 15.6 | 22.3 | 20.3 | 20.3 | 21.4 |
EBITDA margin, IFRS (%) | 25.2 | 34.4 | 28.9 | 26.5 | 30.2 |
CORE EBITDA margin (%) | 30.8 | 32.1 | 29.8 | 30.2 | 31.6 |
Net margin (%) | 54.4 | 19.5 | 9.7 | 11.6 | -4.2 |
Balance Sheet
| Metric | FY2021 | FY2022 | FY2023 | FY2024 | FY2025 |
|---|---|---|---|---|---|
Total assets (CHF Mn) | 16,459 | 17,356 | 16,848 | 19,733 | 17,907 |
Cash & short-term investments (CHF Mn) | 3,184 | 2,224 | 1,669 | 1,711 | 719 |
Short-term debt incl. current LTD (CHF Mn) | 169 | 678 | 192 | 468 | 309 |
Long-term debt (CHF Mn) | 2,234 | 1,554 | 2,637 | 4,350 | 4,015 |
Total debt incl. leases, S&P (CHF Mn) | 2,749 | 2,587 | 3,160 | 5,228 | 4,679 |
Net debt, Lonza definition (CHF Mn) | -958 | -186 | 922 | 2,859 | 3,258 |
Shareholders' equity incl. minorities (CHF Mn) | 9,823 | 10,665 | 9,512 | 9,388 | 7,966 |
Goodwill (CHF Mn) | 2,986 | 2,863 | 2,752 | 3,370 | 1,960 |
Other intangibles (CHF Mn) | 2,454 | 2,231 | 1,988 | 2,002 | 328 |
Working capital (CHF Mn) | 3,585 | 2,637 | 2,139 | 1,861 | 3,209 |
PP&E (CHF Mn) | 4,694 | 6,120 | 6,617 | 8,532 | 8,304 |
Cash Flow
| Metric | FY2021 | FY2022 | FY2023 | FY2024 | FY2025 |
|---|---|---|---|---|---|
Operating cash flow (CHF Mn) | 1,217 | 1,020 | 1,388 | 1,274 | 1,156 |
Capital expenditure (CHF Mn) | 1,301 | 1,826 | 1,648 | 1,381 | 1,321 |
Free cash flow, S&P = OCF − CapEx (CHF Mn) | -84 | -806 | -260 | -107 | -165 |
Share repurchases, net (CHF Mn) | 174 | 51 | 1,011 | 717 | 507 |
Dividends paid (CHF Mn, derived est.) | 223 | 223 | 257 | 286 | 282 |
Cash acquisitions (CHF Mn) | 48 | 10 | 93 | 1,075 | 56 |
Returns & Leverage Ratios (%) and Financial Ratios (x)
| Ratio | FY2021 | FY2022 | FY2023 | FY2024 | FY2025 |
|---|---|---|---|---|---|
ROE, year-end equity (%) | 30.0 | 11.4 | 6.9 | 6.8 | -3.5 |
ROA, year-end assets (%) | 17.9 | 7.0 | 3.9 | 3.2 | -1.5 |
Current ratio (x) | 2.51 | 1.86 | 1.77 | 1.52 | 1.89 |
Debt/equity, total debt (x) | 0.28 | 0.24 | 0.33 | 0.56 | 0.59 |
Net debt / CORE EBITDA (x, Lonza AR2025 series) | -0.6 | -0.1 | 0.5 | 1.7 | 1.6 |
Asset turnover (x) | 0.33 | 0.36 | 0.40 | 0.28 | 0.36 |
Days inventory outstanding (days, derived) | 166 | 175 | 134 | 181 | 147 |
Days sales outstanding (days, derived) | 63 | 69 | 62 | 86 | 59 |
Days payables outstanding (days, derived) | 53 | 46 | 40 | 49 | 45 |
Cash conversion cycle (days, derived) | 176 | 198 | 156 | 218 | 161 |
Financial Analysis
| Ratio | Period | Value | Source |
|---|---|---|---|
ROIC | TTM Jun 2026 | 11.2% | S&P/StockAnalysis |
ROE | TTM Jun 2026 | 12.9% (continuing-earnings basis per S&P) | S&P/StockAnalysis |
Interest coverage (EBIT / net financial result) | FY2025 | 8.9x (1,239 / 140, derived) | FY2025 FYR; AR2025 |
Interest coverage | FY2024 | 4.6x (908 / 199, derived) | FY2025 FYR; AR2025 |
Interest coverage (S&P) | TTM Jun 2026 | 10.2x | S&P/StockAnalysis |
Net debt / equity | FY2025 | 0.4x (Lonza) | FY2025 FYR |
Effective tax rate | TTM | 17.8% | S&P/StockAnalysis |
Revenue by Region
| Region, MarketScreener aggregator (CHF Mn, unreconciled) | FY2021 | FY2022 | FY2023 | FY2024 | FY2025 |
|---|---|---|---|---|---|
United States | 2,117 | 2,415 | 2,136 | 2,309 | 2,525 |
Switzerland | 656 | 996 | 1,168 | 719 | 963 |
United Kingdom | 170 | 139 | 171 | 239 | 212 |
Rest of Europe | 218 | 207 | 195 | 183 | 32 |
Rest of Asia | 31 | 36 | 29 | 28 | 8 |
Share Price and Margin Analysis (%)
| Metric | FY2022 | FY2023 | FY2024 | FY2025 |
|---|---|---|---|---|
Year-end share price (CHF) | 452.9 | 353.7 | 535.8 | 537.8 |
Calendar-year price change (%) | -40.6 | -21.9 | 51.5 | 0.4 |
Share Price & Returns
| Period | Performance | Source |
|---|---|---|
Last price | CHF 565.60 (2 Oct 2026) | S&P/StockAnalysis |
YTD 2026 | ≈ +5.2% (vs 537.8 YE2025, derived) | Derived |
1-year | +5.8% | S&P/StockAnalysis |
3-year | ≈ +60% from YE2023 (353.7) to Oct 2026 (derived; not an exact 36-month figure) | Derived |
50-day / 200-day MA | CHF 566.4 / CHF 531.1 | S&P/StockAnalysis |
Beta (5Y) | 0.81 | S&P/StockAnalysis |
Average daily volume | ~133k shares (20-day); 138,868 avg in 2025 | S&P; AR2025 |
Valuation Multiples
| Multiple | Lonza |
|---|---|
P/E trailing | 36.6x (on S&P earnings basis) |
P/E forward | 27.9x |
EV/EBITDA (TTM) | 17.8x |
EV/Sales (TTM) | 6.3x |
P/B | 4.85x |
P/TBV | 6.8x |
PEG | 1.42 |
FCF yield | 0.5% (S&P FCF basis) |
Dividend yield | 0.88% |
Per-Share Data
| Metric | FY2021 | FY2022 | FY2023 | FY2024 | FY2025 |
|---|---|---|---|---|---|
Dividend per share (CHF) | 3.00 | 3.50 | 4.00 | 4.00 | 5.00 |
Credit Ratings
| Agency | Rating | Outlook | Source |
|---|---|---|---|
S&P Global Ratings | BBB+ | Stable | Lonza bond releases 2024; credit info page (last changed Jan 2019) |
Moody's | Not rated / not disclosed | — | — |
Fitch | Not rated / not disclosed | — | — |
Capital Instruments
| Instrument | Issuer | Coupon | Amount | Maturity |
|---|---|---|---|---|
Swiss straight bond | Lonza Swiss Finanz AG | 0.35% | CHF 150m | 22 Sep 2026 (scheduled) |
Term loan (syndicated) | Lonza | Floating | USD 200m | 2026 |
Swiss straight bond | Lonza Swiss Finanz AG | 2.25% | CHF 185m | 16 May 2028 |
Swiss straight bond | Lonza Swiss Finanz AG | 2.10% | CHF 450m | 12 Sep 2029 |
Eurobond (EMTN) | Lonza Finance International NV | 3.25% | EUR 600m | 4 Sep 2030 |
Swiss straight bond | Lonza Swiss Finanz AG | 2.60% | CHF 215m | 16 May 2031 |
Eurobond (EMTN) | Lonza Finance International NV | 3.875% | EUR 500m | 25 May 2033 |
Eurobond (EMTN) | Lonza Finance International NV | 3.50% | EUR 600m | 4 Sep 2034 |
Eurobond (EMTN) | Lonza Finance International NV | 3.875% | EUR 1,000m | 24 Apr 2036 |
Revolving credit facility | Lonza | Floating | CHF 1,000m (undrawn headroom) | — |
“—” = not publicly disclosed.
Analyst Conclusions
Management guidance (FY2026, as of 22 Jul 2026):
-
CER sales growth of 11–12%;
-
CORE EBITDA margin of 33–34% (raised);
-
FX headwind of –2 to –3% on sales;
-
CapEx intensity in the middle of the mid-to-high-teens range;
-
H2 growth and margins lower than H1 because of AS phasing, Vacaville shutdown and a higher prior-year base;
-
CHI (discontinued): mid-single-digit CER growth; closing before YE2026, then a CHF 500m buyback.
Consensus expectations: about 10.8% p.a. revenue growth and about 20% p.a. EPS growth over three years; average target CHF 688 (S&P/StockAnalysis).
Bull case:
-
Margin structurally re-based upward. CORE EBITDA margin moved from 29.8% (2023) to 34.8% (H1 2026). AS runs at 41–48% and SM recovered to 28% in H1 2026. As Visp large-scale and Vacaville fill under the five-plus commercial contracts and the multi-billion-CHF US collaboration, operating leverage could push group margins toward the mid-30s sustainably. CapEx intensity falling to the mid-to-high teens would turn FCF (CHF 545m CDMO in FY2025) into a compounding story.
-
Geopolitics favour Lonza. As the largest US biologics CDMO with Swiss-based ADC integration, Lonza is a prime beneficiary of supply regionalization and of US customers de-risking from Chinese CDMOs. WuXi-type peers face structural headwinds.
-
Pure-play re-rating and optionality. The CHI exit removes a sub-30%-margin, lower-growth business. It brings CHF 1.7bn upfront plus upside to at least CHF 3bn total, funds bolt-ons and a CHF 500m buyback, and simplifies the equity story toward premium CDMO multiples.
Bear case:
-
Growth decelerates sharply in H2 2026 and 2027. H1 2026 was flattered by phasing and a low base. Vacaville is flat and goes into shutdown, AS margins normalize, and the shares fell about 4% on H1 results despite a margin beat. With low-teens organic growth as the model, a forward P/E of about 28x and EV/EBITDA of about 18x leave little room for a miss.
-
Capital intensity and returns remain mediocre. S&P-basis FCF was negative every year from 2021 to 2025. TTM ROIC is about 11% against a WACC of about 8%. Statutory ROE has been single-digit or negative since 2023. The Capsugel round-trip shows a history of capital misallocation, and Vacaville's full potential is a next-decade story.
-
Execution and leadership risk persists. Cell & Gene performance has been volatile. Big pharma's US in-house CapEx wave and Samsung's capacity build could erode utilization and pricing. Board and executive renewal is rapid (average board tenure about 1.3 years; new CCO from 2027) during a period of complex separation and large project delivery (Stein 2028/2030, Visp 2028).
Concluding analyst verdict.
Lonza enters late 2026 as a cleaner, more profitable and more strategically coherent company than at any point in the past decade. The CHI sale, three smaller divestments and the One Lonza reorganization have turned a conglomerate-tinged supplier into a pure-play CDMO.
The evidence of operating improvement is concrete:
-
continuing sales grew 21.7% CER in FY2025;
-
the CORE EBITDA margin moved from 30.2% to 31.6%, then to 34.8% in H1 2026, with full-year guidance raised to 33–34%;
-
the Advanced Synthesis platform now earns returns rivalling the best in contract manufacturing.
Lonza's strategic positioning is unusually strong. It combines the broadest modality coverage in the industry, the largest US biologics footprint at a time when customers want regional supply, and a vertically integrated Swiss ADC chain backed by customer commitments.
The equity case is not without friction. Statutory returns have lagged the narrative, and S&P-basis free cash flow was negative throughout 2021–2025 as about CHF 7.5bn went into CapEx and a large acquisition. Management's own guidance implies a visibly weaker second half. At about 28x forward earnings and about 18x EV/EBITDA, the shares already discount a good part of the margin story. The July 2026 sell-off on a margin beat shows how sensitive the stock is to growth cadence. Leadership and board renewal has been rapid, and Cell & Gene and Vacaville still need to prove their economics.
Overall, Lonza looks like a high-quality compounder in transition from build to harvest. The decisive variable for the next 12–24 months is cash conversion, not growth. If CapEx intensity normalizes to the mid-to-high teens while margins hold in the 33–35% band, operational FCF should step up materially and justify the premium. The CHI proceeds and buyback provide downside support. The verdict is constructive, with valuation-driven patience. The data supports a positive fundamental stance, but entry discipline around H2 2026 phasing and the first pure-play FY2027 guidance is warranted.
All figures are from public sources as cited and are current as of 7 October 2026.
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View Subscription PlansExecutive Leadership
Executive Leadership Team
| Name | Title | Tenure / key background (where verified) |
|---|---|---|
Dr. Wolfgang Wienand | Chief Executive Officer | CEO since 1 Jul 2024; previously CEO of Siegfried Holding (2019–2024). Age ~54 (Simply Wall St). |
Philippe Deecke | Chief Financial Officer | Holds ~0.0049% of shares (Simply Wall St). |
Maria Soler Nunez | Chief Quality Officer | Previously led Group Operations (AR2025 references her foundation-laying in Operations). |
Nicoleta Baumgärtner | Chief Human Resources Officer | — |
Andreas Bohrer | Chief Legal & Corporate Affairs Officer | ~11.6 years with Lonza. |
Jason Berndt | Head of Group Operations (EVP) | Appointed within the last year (Simply Wall St). |
Gordon Bates | Head of Integrated Biologics | Previously President and Head of Small Molecules. |
Christian Seufert | Head of Advanced Synthesis | — |
Daniel Palmacci | Head of Specialized Modalities | Previously President, Cell & Gene. |
Jean-Christophe Hyvert | Head of Capsules & Health Ingredients | Expected to depart with CHI at closing; former President, Biologics and Cell & Gene. |
Directors' Remuneration
| Item | FY2024 | FY2025 |
|---|---|---|
CEO total compensation (CHF Mn) | 6.42 | 5.72 |
Executive Committee aggregate (CHF Mn) | 21.6 | 23.0 |
Board of Directors aggregate (CHF Mn) | 2.76 | 3.34 |
Board of Directors
| Name | Role | Notes |
|---|---|---|
Jean-Marc Huët | Chair | Re-elected Chair at AGM 8 May 2026. |
Claudia Süssmuth-Dyckerhoff | Vice-Chair (independent) | Elected AGM 2026; healthcare and life-sciences board experience. |
Christoph Mäder | Lead Independent Director | — |
Juan Andres | Independent | — |
Sami Atiya | Independent | Elected AGM 2026. |
Eric Drapé | Independent | Elected AGM 2025. |
Stephen Fry | Independent | Elected AGM 2026. |
Marion Helmes | Independent | — |
Angelica Kohlmann | Independent | — |
David Meline | Independent | — |
Major Shareholders
| Rank | Holder | Stake (%) | Source / date |
|---|---|---|---|
| 1 | BlackRock, Inc. | 9.85 (notified) / 9.91–9.96 (aggregator) | AR2025; Simply Wall St 2026 |
| 2 | UBS Asset Management / UBS Fund Mgmt (CH) | 6.25–6.32 | AR2025; Simply Wall St |
| 3 | The Vanguard Group | 3.0–4.35 | Simply Wall St (varies by listing view) |
| 4 | Norges Bank Investment Management | ~3.15 (below 3% notification threshold by YE2025 per AR) | Simply Wall St; AR2025 |
| 5 | Invesco Ltd. | ~1.2–1.4 | Simply Wall St |
| 6 | JP Morgan Asset Management | ~1.2 | Simply Wall St |
| 7 | Pictet Asset Management | ~1.1–1.2 | Simply Wall St |
| 8 | Baillie Gifford & Co. | ~1.2 | Simply Wall St (Aug 2026 view) |
| 9 | Amundi Asset Management | ~1.0 | Simply Wall St |
| 10 | Comgest S.A. / Union Investment | ~0.8–0.9 | Simply Wall St |
Competitive Landscape
Peer Comparison
| Platform | Key competitors |
|---|---|
Integrated Biologics (mammalian DS/DP) | Samsung Biologics (KR); WuXi Biologics (CN); Fujifilm Diosynth Biotechnologies (JP/US/EU); Boehringer Ingelheim BioXcellence (DE); Thermo Fisher Patheon Pharma Services (US); AGC Biologics (JP/US/EU); Celltrion (CMO activity); Rentschler (DE); Celonic (CH/DE); National Resilience (US) |
Advanced Synthesis (small molecules, ADC/bioconjugates, HPAPI) | WuXi AppTec / WuXi STA (CN); WuXi XDC (CN, ADC); Siegfried (CH); Cambrex (US, Permira-owned); Asymchem (CN); Piramal Pharma Solutions (IN); Recipharm (SE, EQT); Corden Pharma (DE/CH); Axplora (FR); Catalent (now Novo Holdings, US); Abzena (ADC) |
Specialized Modalities (C&G, microbial, mRNA, Bioscience) | Charles River (C&G manufacturing); Minaris (ex-Hitachi/Resonac, now private); Oxford Biomedica (UK, vectors); Catalent Gene Therapy (Novo); AGC Biologics; Fujifilm (microbial); Thermo Fisher (viral vectors; Bioscience reagents); Merck KGaA / MilliporeSigma (Bioscience reagents, ADC Bioconjugates); Sartorius (media, tools) |
Peer Comparison FY2025
| Metric | Lonza (FY2025, continuing) | Samsung Biologics (FY2024) | WuXi Biologics (FY2024) | Siegfried (FY2024) |
|---|---|---|---|---|
Revenue | CHF 6,531m | ~KRW 4.5tn (~CHF 2.9bn) | ~RMB 18.7bn (~CHF 2.3bn) | ~CHF 1.3bn |
Revenue growth | +21.7% CER | ~+23% | ~+9% | low single digit |
Profitability | CORE EBITDA margin 31.6% (H1 2026: 34.8%) | Operating margin ~29% | — | — |
R&D intensity | ~1.5–2% (aggregator) | — | — | — |
Listing | SIX / SGX | KRX | HKEX | SIX |
Notes | Broadest modality coverage; largest US biologics CDMO | Pure mammalian scale leader in Asia (Plant 5 onward) | US Biosecure Act exposure | Small molecules / DP only |



