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Senior CSV Specialist — Cell Therapy GMP Expert
Job in
Raritan, Somerset County, New Jersey, 08869, USA
Listed on 2026-07-31
Listing for:
Merck & Co.
Full Time
position Listed on 2026-07-31
Job specializations:
-
Pharmaceutical
Validation Engineer, Regulatory Compliance Specialist, Pharmaceutical Manufacturing, Quality Engineering
Job Description & How to Apply Below
Legend Biotech is seeking a Sr. CSV Specialist to join the Manufacturing & Supply team in Raritan, NJ. The role provides commissioning, qualification and validation support for computerized systems in CAR-T cell therapy manufacturing, ensuring data integrity and regulatory compliance.
You will own CSV/CQV protocols, manage complex projects, and collaborate with SAP, MES, and other systems, with emphasis on CQV and risk assessments. Strong GMP knowledge and team leadership are essential.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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