Merck is seeking a Regulatory Affairs professional to lead global regulatory strategies for assigned pharmaceutical products. You will author and review CMC submission components for approvals and variations, coordinate with manufacturing divisions and external CMOs, and assess regulatory risks to ensure conformance. The role requires experience with Veeva and strong communication skills. Hybrid work arrangement in the United States, with salary range reflecting seniority, and eligibility for

Also on the board Same function, level within a rung

Level

Manager

Location

North Wales, PA

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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