Research Scientist • Senior

Who you are

You have a strong background in biotechnology and experience in upstream process development, particularly in the context of viral vector processes. You are comfortable working in a laboratory setting and have a keen understanding of GMP compliance and technology transfer. Your ability to develop and scale-up processes is complemented by your analytical skills, allowing you to evaluate and optimize methodologies effectively.

You thrive in collaborative environments and are adept at communicating complex scientific concepts to both technical and non-technical stakeholders. Your experience in a fast-paced biotechnology setting has equipped you with the skills to manage multiple projects simultaneously while maintaining a focus on quality and compliance. You are committed to continuous learning and staying updated with the latest advancements in the field.

Desirable

Experience with cell and gene therapy processes is a plus, as is familiarity with regulatory requirements for biologics development. A background in working with cross-functional teams to drive projects from research to commercialization will set you apart. You are also encouraged to bring innovative ideas to the table, contributing to the overall mission of improving human health through biotechnology.

What you'll do

In this role, you will lead the development and optimization of upstream processes for viral vector production. You will be responsible for translating research findings into scalable manufacturing processes that comply with GMP standards. Your work will involve designing experiments, analyzing data, and collaborating with other scientists and engineers to ensure successful technology transfer.

You will also play a key role in troubleshooting and resolving issues that arise during the manufacturing process, ensuring that production timelines are met without compromising quality. Your contributions will directly impact the efficiency and effectiveness of our drug development efforts, helping to accelerate the delivery of innovative therapies to patients.

Collaboration is essential in this position, as you will work closely with various departments, including quality assurance, regulatory affairs, and project management. You will participate in meetings to discuss project progress, share insights, and align on objectives. Your ability to communicate effectively will be crucial in fostering a productive team environment.

What we offer

GenScript offers a supportive and inclusive workplace where you can grow your career in biotechnology. We provide opportunities for professional development and encourage our employees to pursue continuous learning. You will be part of a mission-driven organization dedicated to making a positive impact on human health.

We value innovation and creativity, and we encourage you to bring your ideas to the table. Our team is committed to collaboration and mutual support, ensuring that everyone has the resources they need to succeed. We also offer competitive compensation and benefits packages to recognize your contributions to our success.