Lonza(LONN)
Basel, SwitzerlandCDMO (Contract Manufacturing)
Focus: Lonza is a global CDMO (Contract Development and Manufacturing Organization) headquartered in Basel, Switzerland, serving biopharmaceutical clients across multiple therapeutic modalities. With 10,001–50,000 employees and a public listing (LONN), it operates at enterprise scale in the outsourced manufacturing sector.
Profile data last refreshed 2h ago · AI intelligence enriched 1w ago
Funding Stage
PUBLIC
Employees
10001-50000
Open Jobs
653+972 this month
Hot — 1370 jobs added in 30d
Net +972 (1370 new, 398 removed). Aggressive expansion phase.
Should You Work at Lonza?
AI assessmentLonza is a stable, scaling CDMO with strong operational hiring—ideal for manufacturing, QA, and engineering careers; less appealing for those seeking early-stage drug development or scientific leadership roles.
Why Work Here
- Large, publicly-traded CDMO with 619 active job openings signals sustained hiring momentum and career stability.
- Heavy investment in Quality Assurance (102 roles) and Manufacturing (90 roles) indicates commitment to operational excellence and regulatory compliance—core competencies in the CDMO sector.
Data completeness
4/9 — Basic
Company HealthSolid
Pipeline
Early-stage
9 total
LOE Risk
Protected
No near-term cliffs
Hiring
Stable
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.
Pipeline & Clinical Trials
L-Carnitine
Healthy VolunteersClinical Trials (1)
NCT02635594Effects of Carnipure® Tartrate on Postprandial Endothelial Function and Recovery
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
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.