Senior Scientist – Cell & Gene Therapy

Responsibilities

• Lead research programs in cell and gene therapy for rare genetic disorders.
• Design and execute preclinical studies for AAV-based gene therapy vectors.
• Develop and optimize viral vector manufacturing processes and analytical assays.
• Prepare IND-enabling study packages and contribute to regulatory strategy.
• Collaborate with academic partners and CROs on translational research programs.

Requirements

• PhD in Molecular Biology, Gene Therapy, Virology, or related field.
• 5-8 years of research experience in cell and gene therapy.
• Expertise in viral vector design, production, and characterization (AAV, lentivirus).
• Experience with GMP-compatible process development for ATMPs.
• Strong publication record and knowledge of ATMP regulatory framework.