Debiopharm
Switzerland - LausanneCDMO (Contract Manufacturing)
Focus: Debiopharm is a Swiss-based CDMO (Contract Development & Manufacturing Organization) specializing in oncology, infectious diseases, and other therapeutic areas with a lean team of 1-50 employees. The company operates as a private entity focused on contract development and manufacturing services rather than proprietary drug development.
Profile data last refreshed 3h ago · AI intelligence enriched 2mo ago
Funding Stage
PRIVATE
Employees
1-50
Open Jobs
12-6 this month
Cooling — net -6 jobs in 30d
6 added, 12 removed. Slower than typical.
Should You Work at Debiopharm?
AI assessmentBest suited for early-stage specialists seeking hands-on CDMO/manufacturing experience and oncology pipeline exposure; avoid if you need structured career progression or large-company resources.
Why Work Here
- Exposure to early-stage oncology pipeline with 14 Phase 1 programs spanning multiple indications from AML to solid tumors
- Diverse therapeutic area coverage across oncology, infectious diseases, endocrinology, cardiovascular, and nephrology enables broad technical skill development
Data completeness
4/9 — Basic
Company HealthStrong
Pipeline
Late-stage
3 Phase 3+
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
Alisporivir
Hepatitis CClinical Trials (1)
NCT01970904Pharmacokinetics, Pharmacodynamics and Safety of DEB025 Plus Ribavirin in Chronic Hepatitis C Genotype 2 and 3 Treatment naïve Patients
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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.