Updated on 17 February 2026
EU GMP Clinical Manufacturing Partner for Phase I Supply
About
We are seeking an EU-based GMP partner to support clinical manufacturing and supply for Phase I, with a focus on execution quality, speed, and clean tech transfer discipline.
Partnership scope can include:
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Optimization for clinical manufacturing readiness and scale-appropriate execution
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GMP batch execution and quality systems alignment
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QC strategy support (release logic, stability approach, documentation)
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CMC documentation contributions suitable for clinical entry
We value partners that are transparent, pragmatic, and comfortable operating on milestone-driven plans. Details can be shared under CDA.
Organisation
Similar opportunities
Expertise
CMC Leadership for Biologics: From Concept to Commercial Manufacturing
- Biotech, Pharma and Cosmetics
Ramtin Rahbar
Co-founder and Chief Technical Officer at Ness Therapeutics
Toronto, Canada
Project cooperation
EU work packages to accelerate Phase I readiness
- Execution
- Technical
- Biotech, Pharma and Cosmetics
Ramtin Rahbar
Co-founder and Chief Technical Officer at Ness Therapeutics
Toronto, Canada
Expertise
Clinical Trial Operations & Project Manager | Clinical Data Manager | Quality & Regulatory Expert
- Healthcare
- Biotech, Pharma and Cosmetics
Madhuparna Ganguly
Clinical Operations & Project Manager | MBA @ SwissTPH | Clinical Research Scientist - QA & RA at University of Geneva
Zurich, Switzerland