Focus: Takeda is a Tokyo-based multinational pharmaceutical company with 49,000 employees specializing in small molecules and enzymes across gastroenterology, rare diseases, neuroscience, and oncology. It is one of the world's largest pharmaceutical companies by headcount and revenue scale.
Profile data last refreshed 38m ago · AI intelligence enriched 1w ago
Hot — 2224 jobs added in 30d
Net +742 (2224 new, 1482 removed). Aggressive expansion phase.
5 recent layoff filings (12 mo) — 637 affected
Source: state DOL filings via Big Local News
Takeda offers a stable Big Pharma foundation with strong current franchises and global reach, but the looming patent cliff (2028–2029) combined with recent layoffs signal near-term restructuring risk; best suited for candidates seeking established-market expertise rather than long-term growth trajectory.
Automated analysis based on publicly available data (FDA, SEC, ClinicalTrials.gov). May be incomplete or delayed. This score does not reflect insider knowledge and should not be used as the sole basis for investment or employment decisions.
Takeda's largest single revenue contributor (26% of revenue), providing a stable cash stream until patent expiry in 2032.
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
Generated by Claude from Takeda's SEC filings, pipeline programs, hiring velocity, FDA actions, and WARN data. Inference, not editorial — verify before quoting.
Second-largest revenue driver; faces patent cliff in 2029, exposing the company to significant revenue erosion in the medium term.
Established neuroscience franchise supporting revenue, though lifecycle stage and patent data indicate no defined expiration in dataset.
Oncology franchise with patent protection until 2033, contributing meaningfully to specialty pharma positioning.
Recent FDA expansion approval for intravenous formulation (June 2026) positions this GI franchise as a growth driver; 16.99M shares granted June 2026 suggest company confidence.
GI market mainstay with patent protection until 2032, contributing to Takeda's gastroenterology portfolio depth.
GI-focused product facing patent expiration in 2028, making it a near-term cliff risk requiring pipeline replacement.
Rare disease franchise supporting niche indication; lifecycle and patent data indicate no defined expiration in dataset.
43 discontinued, 19 duplicate formulations not shown
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Takeda Pharmaceutical FY Pretax Loss Y142.36B Vs Pft Y175.08B - Moomoo
Takeda Pharmaceutical FY Pretax Loss Y142.36B Vs Pft Y175.08B Moomoo
Largest Mass. biotech employer is axing thousands of jobs. Cambridge employees are next - MassLive
Largest Mass. biotech employer is axing thousands of jobs. Cambridge employees are next MassLive
Is Zasocitinib’s Phase 3 Beat And New Shelf Filing Altering The Investment Case For Takeda Pharmaceutical (TSE:4502)? - simplywall.st
Is Zasocitinib’s Phase 3 Beat And New Shelf Filing Altering The Investment Case For Takeda Pharmaceutical (TSE:4502)? simplywall.st
Takeda’s zasocitinib bests Sotyktu in phase III psoriasis trial - BioWorld News
Takeda’s zasocitinib bests Sotyktu in phase III psoriasis trial BioWorld News
Fierce Pharma Asia—Astellas CEO’s 5-year plan; Takeda’s psoriasis win; RA’s China bridge program - Fierce Pharma
Fierce Pharma Asia—Astellas CEO’s 5-year plan; Takeda’s psoriasis win; RA’s China bridge program Fierce Pharma
Showing 6 of 10 news items
Based on last 4 crawl cycles
Source: USCIS H-1B Employer Data Hub
Recent peer-reviewed publications with author affiliations at this company
Analysis of healthcare resource utilization before and after initiation of maribavir for cytomegalovirus treatment.
Bleeding rates, healthcare utilization, and costs among patients with hemophilia a without inhibitors treated with concomitant octocog alfa or extended half-life factor VIII while on emicizumab prophylaxis.
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Source: state DOL filings, aggregated via Big Local News
Cambridge-based R&D roles face significant attrition risk; restructuring appears tied to pipeline deprioritization ahead of patent cliffs; candidates should clarify program viability and site stability during interviews.
Showing 5 of 10 publications
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