Senior CQV Specialist – Cell Therapy Manufacturing
Job in
Raritan, Somerset County, New Jersey, 08869, USA
Listed on 2026-09-03
Listing for:
Merck & Co.
Full Time
position Listed on 2026-09-03
Job specializations:
-
Manufacturing / Production
Validation Engineer, Pharmaceutical Manufacturing, Regulatory Compliance Specialist
Job Description & How to Apply Below
Legend Biotech USA Inc. is seeking a Sr. CQV Specialist in Raritan, NJ to support cGMP cell therapy manufacturing. You will lead commissioning, qualification, and validation activities across the plant, ensuring data integrity and compliance with regulatory standards.
You will coordinate with cross-functional teams, manage vendor relations and contribute to audits. A Bachelor’s degree in a relevant field and 7+ years’ experience in aseptic manufacturing are required.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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