GenScript
A senior QC scientist role within GenScript/ProBio's CDMO supporting development and optimization of a GMP QC analytics laboratory for cell and gene therapy products. The position focuses on characterization and release testing of engineered cell lines and viral vectors, ensuring regulatory and biosafety compliance while supporting CMC activities and technology transfer. The role reports to the Sr. QC Manager and involves collaboration with cross-functional teams and occasional travel to support projects.
Headquarters
Piscataway, New Jersey, United States
Company Size
5001-10000 employees
Founded
2002
GenScript is a global biotechnology company that supplies synthetic genes, peptides, proteins, antibodies and a broad catalog of life-science reagents and assay tools. It also provides custom services across discovery and development—gene synthesis, peptide/protein production, antibody discovery and engineering, CRISPR genome‑editing reagents, cell‑line development, and biologics CDMO capabilities. Academic labs, biotech and pharma customers rely on GenScript for scalable, quality‑controlled reagents and end‑to‑end contract services with rapid turnaround and online ordering.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for GenScript.
GenScript ProBio and Comprehensive Cell Solutions, a Business Unit of the New York Blood Center Enterprises, Form a Pioneering Partnership to Expedite Cell and Gene Therapy Development and Manufacturing
Jun 7, 2023
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