This position manages the complete lifecycle of critical reagents—including reference standards, positive controls, anti-sera, and other critical materials—used in the release and stability testing of vaccine and biological products. Responsibilities span reagent acquisition, certification and qualification testing, implementation, ongoing monitoring, and replacement as needed. The role applies GMP/GLP requirements and supports regulatory submissions and inspection readiness. It is a full-time, permanent position with a Monday–Friday, 8 a.m.–5 p.m. schedule. Candidates within commuting distance of West Point, Pennsylvania are encouraged to apply.
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Job Type
Full-time
Career Level
Mid Level