Merck
A leading pharmaceutical company seeks a Senior Specialist, Regulatory Authoring Business Analyst to enhance regulatory authoring processes by optimizing data management and mapping workflows. This role involves collaboration with cross-functional teams to implement digital solutions, ensuring efficient execution and compliance in operations. Applicants should possess extensive experience in regulatory authoring, project management skills, and knowledge of manufacturing processes. A comprehensive benefits package and competitive salary range of $114,700 - $180,500 are offered.
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