As a Development Scientist, you’ll optimize production methods for viral vectors and ensure smooth operations during peak demand.
You’ll also take on key responsibilities for the high-revenue LentiBOOST™ product by providing scientific support, while mentoring and training top-tier Quality Control and Production teams.
Plus, you’ll have the chance to explore automation opportunities, such as using a liquid handler for small-scale rAAV manufacturing, unlocking new revenue streams and advancing the field of gene therapy.

QUALIFICATIONS:

• Ph.D., Master’s degree, or equivalent experience in Virology, Biotechnology, or Quality Assurance.
• Experience with tools like Design of Experiments (DoE) and automation processes for manufacturing.
• A clear understanding of regulatory requirements, especially in Good Manufacturing Practices (GMP), and how they apply to viral vector production and clinical trials.
• Strong organizational and communication skills.
• A collaborative mindset and the ability to work effectively in multidisciplinary teams.
  Take the chance to develop your skills in an exciting environment, implement new technologies, and make a real impact on the future of gene therapy. If you’re ready to take your career to the next level and make a significant contribution, we look forward to hearing from you!

• Oversee production processes to address challenges related to scalability.
• Optimize viral vector production and purification methods using Design of Experiments (DoE) and automation techniques.
• Support Lentiboost technology by managing manufacturing, inventory, customer inquiries, and GMP service providers.
• Develop, update, and review SOPs, providing hands-on training to Quality Control, R&D, and Manufacturing teams.
• Assist with technical documentation, patent inquiries, audits, and transduction performance tests.