Post-Doc – Innovative manufacturing concepts on Biologics (all genders) (full-time, temporary for 24 months)
Core
Design, execute, and assess studies to identify key risks and mechanisms for co-formulating biologics in parenteral drug products during early clinical stages.
Role type
Post-Doc in pharmaceutical manufacturing process development
Builds
Robust manufacturing processes for biologics drug products
Domain
Biopharmaceuticals / Parenteral drug development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Experimental design, statistical data evaluation, root cause analysis, aseptic handling, protein aggregation detection, particle characterization, complex equipment operation
Preferred skills
Protein aggregation work experience, analytical methods for protein denaturation, German language skills
Technologies
Analytical instruments for protein characterization, aseptic processing equipment
Responsibilities
Plan and perform systematic studies on innovative formulation concepts; Publish results in peer-reviewed journals and present at conferences; Collaborate with international multidisciplinary teams; Participate in root cause analyses of development projects; Maintain scientific standards and safe laboratory practices; Engage with scientific literature to apply insights to projects
Seniority
Post-Doc, independent researcher