Director of Regulatory Inspection Readiness

L7

celldex therapeuticsHampton, NJyesterday
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.
Apply now
Apply now

Level

ManagerL7

Location

Hampton, NJ

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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