Senior Associate, Gene Therapy focusing on Functional Characterization | Senior Associate (m/w/d) Gene Therapy mit Fokus auf funktionaler Charakterisierung

Roche Diagnostics GmbH

Penzberg, Bayern, Deutschland
Published Feb 9, 2026
Full-time
Fixed-term

Job Summary

This Senior Associate role within Pharma Technical Characterization Gx (PTCG) actively shapes the future of medical care by driving the technical development of in vivo gene therapeutics during preclinical and clinical phases. The position acts as a critical link between pharmaceutical research and quality control for market products. Key responsibilities include pioneering innovation by scouting, evaluating, and implementing novel analytical methods, such as digital PCR, functional bioassays, and Next-Generation Sequencing (NGS), specifically for analyzing viral vectors (primarily rAAV). You will independently conduct complex experiments, ranging from method development and equipment qualification to test validation under strict GMP requirements. The ideal candidate holds a degree in a relevant scientific field (e.g., Virology, Biochemistry) and brings over three years of practical experience in molecular biology or virology, coupled with deep expertise in cell culture, flow cytometry, and various PCR techniques. This is an opportunity to join a highly motivated, agile, and interdisciplinary team dedicated to developing smart solutions for the next generation of therapeutic modalities.

Required Skills

Education

Degree in Chemistry, Biochemistry, Biology, Virology, Pharmacy, or a comparable scientific field

Experience

  • More than 3 years of practical and theoretical experience in Molecular Biology or Virology
  • Professional experience in Digital Health or Diagnostics (ideally)
  • Experience with method development, equipment qualification, and test validation under GMP requirements
  • Experience in defining control and testing strategies for gene therapy vectors

Languages

German (Fluent)English (Fluent)

Additional

  • Fixed-term contract for 2 years; Familiarity with GMP principles, including data integrity and method validation