Celldex Therapeutics, Inc. seeks an experienced Director to lead the inspection management program, ensuring readiness for FDA/ international inspections and partner audits. You will coordinate across Quality, Manufacturing, Supply Chain, Regulatory Affairs, Clinical Development, and Commercial functions to support a transition to commercial readiness. The role requires a strong background in GMP compliance, regulatory inspections, and CAPA management, with global CMOs experience preferred.

Also on the board Same function, level within a rung

Level

Manager

Location

Hampton, NJ

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

today

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