Merck
A leading pharmaceutical company is seeking a Senior Specialist, Regulatory Authoring Business Analyst. The role involves optimizing regulatory authoring processes and enhancing data management within a hybrid work model. Candidates should have a minimum of 5 years experience in regulatory submission documentation and a Bachelor's degree in a related field. The role includes business process mapping, stakeholder management, and project oversight, ensuring efficient and compliant CMC operations. A comprehensive benefits package is offered.
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