GenScript · 2 months ago
(Sr). Scientist, Upstream Process Development
Pennington, NJ
Full-time
Onsite
Mid, Senior Level
$80K/yr - $110K/yr
3+ years expGenScript Biotech Corporation is a global biotechnology group committed to improving health through biotechnology. The Scientist in Upstream Process Development will lead the translation of research processes to GMP-compliant manufacturing, focusing on developing and optimizing viral vector processes in a fast-paced environment.
BiotechnologyGeneticsManufacturing
Responsibilities
Conduct hands-on experimental work in the development of upstream unit operations (cell culture, transfection, and harvest/clarification) for viral vector (AAV, LVV) manufacturing process
Design, execute, and analyze cell culture experiments using Design of Experiments (DOE) principles and report data summary packages
Collaborate with internal/external partnerships to evaluate and implement new bioprocessing technologies and strategies
Develop and optimize process parameters to improve yield, quality, and consistency of viral vector production with guidance
Independently follow detailed and comprehensive project timelines
Support/drive the start up of AAV/LVV lab operations including, but not limited to: Draft, review, and approval of Standard Operating Procedures (SOPs), Implementation of Lean 6 sigma/5s best practices, and streamlining material flow
Present updates to project or cross functional teams on process development and manufacturing support activities
Read and understand scientific literature in gene and cell therapy, use the knowledge to generate ideas and contribute to process design and development
Perform other duties as assigned based on business needs
Qualification
Required
Bachelor's degree with 5-7 years, or Master's Degree with 3-7 years, or Ph.D. degree with 0-3 years' experience in Biology, Biochemistry, Chemical Engineering or equivalent with particular experience in gene and cell therapy product design
Experience with AAV and/or lentiviral vector production systems
Strong understanding of process scale-up, cGMP manufacturing technology transfer, and manufacturing support
Prior experience with cGMP manufacturing environment
Familiarization with analytical methods for viral vector characterization (qPCR, ELISA, HPLC)
Familiarization of regulatory requirements for gene therapy products (FDA, EMA)
Excellent organizational and project management abilities
Strong analytical and problem-solving skills with attention to detail
Strong interpersonal, verbal, and written communication skills
Company
GenScript
GenScript USA, Inc. is a leading contract research organization (CRO) specialized in biological research and drug discovery/development
5001-10000 employees
H1B Sponsorship
GenScript has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (38)
2024 (28)
2023 (19)
2022 (11)
2021 (11)
2020 (12)
Funding
Current Stage
Public CompanyTotal Funding
unknown2015-12-31IPO
Leadership Team
Larry Wang
Co-Founder & Board Director
Shiniu Wei
Chief Financial Officer
Recent News
Morningstar.com
2025-11-10
Company data provided by crunchbase