Scientist I - Upstream Process Development

Are you a passionate scientist eager to advance the field of gene therapy? We are seeking a talented Scientist I to join a dynamic Upstream Process Development team, where you will play a key role in designing, optimizing, and scaling viral vector manufacturing processes.

This is an exciting opportunity to contribute to both internal and external client programs, developing cutting-edge technology and platforms for viral vector production. If you thrive in a collaborative environment and are driven by scientific excellence, we want to hear from you!

Your Impact:

• Design and execute experiments to develop, optimize, and scale upstream processes for gene therapy projects.
• Collaborate with cross-functional teams to integrate upstream processes with downstream processes and analytical methods.
• Evaluate and implement innovative technologies and methodologies to enhance process efficiency and productivity.
• Analyze and interpret experimental data, troubleshoot process issues, and make data-driven recommendations for process improvements.
• Document all experiments, results, and procedures in a clear and organized manner to ensure compliance with GDP standards.
• Stay current with industry trends and research to maintain a high level of scientific knowledge and expertise.
• Mentor, manage, and support junior team members, contributing to a collaborative and productive work environment.
• Present development updates to clients and align on delivery of key project milestones.

What You Bring:

• Ph.D. in a relevant scientific discipline (e.g., Bioprocess Engineering, Cell Biology, Biochemistry, or related field) with 0-2 years industry experience, a Masters degree with 2-4 years of industry experience, or a Bachelors degree with 3-5 years industry experience.
• Proven experience in developing upstream processes for gene therapies and/or viral vector production (bioreactors, expansion/feeding strategies, and harvest unit operations).
• Ability to scale fermentation/suspension cell culture systems from benchtop to clinically relevant scales.
• Strong understanding of cell and gene therapy and regenerative medicine concepts.
• Excellent analytical and problem-solving skills with a demonstrated ability to work independently and as part of a team.
• Proficient in DOE, data analysis and statistical software (JMP experience desired).
• Knowledge of cGMP, QBD and regulatory requirements is a plus.
• Strong communication skills, both written and verbal.
• Exceptional attention to detail and a commitment to quality in all aspects of work.