Senior CQV Specialist: Cell Therapy Manufacturing

A leading biotechnology company is seeking a Sr. CQV Specialist in Raritan, NJ. This role supports the cGMP Cell Therapy Manufacturing plant, focusing on validation and compliance. Responsibilities include executing CQV protocols, managing projects, and supporting technical investigations. Candidates should have a Bachelor’s degree, 7+ years of experience in aseptic manufacturing, and proficiency with Microsoft ERP and testing systems. Competitive compensation and comprehensive benefits are offered, including a performance bonus and equity.
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