Merck
A leading pharmaceutical company is seeking a Senior Specialist, Regulatory Authoring Business Analyst to optimize regulatory authoring processes. The role involves mapping workflows, prioritizing source documents for digitization, and collaborating with cross-functional teams to implement digital solutions. Candidates should have a strong background in manufacturing processes and regulatory requirements, with a minimum of a Bachelor's degree in a related field and at least 5 years of relevant experience. This position offers an opportunity to contribute to a digital transformation initiative.
#J-18808-Ljbffr