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Home›Jobs›GenScript›(Sr). Scientist, Downstream Process Development
GenScript

About GenScript

Empowering biotech with innovative gene synthesis solutions

🏢 Corporate, Tech👥 1K-5K📅 Founded 2002📍 Piscataway, New Jersey, United States

Key Highlights

  • Headquartered in Piscataway, NJ, with a global presence
  • Serves over 20,000 customers, including top pharma companies
  • Raised over $200 million in funding to date
  • Employs 1,000-5,000 professionals in biotech

GenScript Biotech Corporation, headquartered in Piscataway, New Jersey, is a leading global biotechnology company specializing in gene synthesis, peptide synthesis, and antibody development. With over 1,000 employees, GenScript serves more than 20,000 customers worldwide, including major pharmaceuti...

🎁 Benefits

GenScript offers competitive salaries, equity options, generous PTO, flexible remote work policies, and comprehensive health benefits to support emplo...

🌟 Culture

GenScript fosters a research-driven culture that emphasizes innovation and collaboration, encouraging employees to contribute to groundbreaking advanc...

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GenScript

(Sr). Scientist, Downstream Process Development

GenScript • Pennington, NJ

Posted 5d ago🏛️ On-SiteSeniorResearch scientist📍 Pennington
Apply Now →

Overview

GenScript is seeking a Senior Scientist in Downstream Process Development to support and lead the translation of research processes to GMP-compliant manufacturing. This role involves developing and scaling up viral vector processes.

Job Description

Who you are

You have a strong background in downstream process development, ideally with experience in viral vector processes. Your expertise in translating research processes into GMP-compliant manufacturing will be crucial in this role. You are comfortable working in a laboratory environment and have a keen understanding of the technical aspects of process development. You thrive in collaborative settings and are eager to contribute to a team focused on advancing biotechnology solutions.

Desirable

Experience in cell and gene therapy, as well as familiarity with regulatory requirements for biopharmaceutical manufacturing, will set you apart. You are proactive in your approach and have a track record of successfully leading projects from research to implementation. Your ability to communicate complex scientific concepts clearly will enhance collaboration with cross-functional teams.

What you'll do

In this role, you will report to the Associate Director of Downstream Viral Vector Process Development & MSAT Department. You will be responsible for developing, scaling up, and evaluating the technology transfer of viral vector processes. Your work will directly impact the efficiency and effectiveness of our manufacturing processes, ensuring that they meet the highest standards of quality and compliance. You will lead efforts to optimize existing processes and implement new technologies that enhance our capabilities in biopharmaceutical development.

You will collaborate closely with other scientists and engineers to troubleshoot and resolve issues that arise during the development and manufacturing phases. Your insights will help shape the direction of our projects, and you will play a key role in mentoring junior team members, sharing your knowledge and expertise to foster their growth.

What we offer

At GenScript, you will be part of a mission-driven organization dedicated to improving human health through biotechnology. We offer a supportive work environment where innovation is encouraged, and your contributions will be valued. You will have access to cutting-edge technologies and resources that will enable you to excel in your role. We are committed to your professional development and provide opportunities for continuous learning and advancement within the company. Join us in making a meaningful impact in the field of biotechnology.

Interested in this role?

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