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Associate Director, Regulatory Affairs - Power Platform Solutions Specialist

Merck
October 1, 2026
Full-time
Remote friendly (North Wales, PA)
Worldwide
IT
Role: Associate Director, Regulatory Affairs – Power Platform Solutions Specialist, focusing on supporting and configuring the Microsoft Power Platform within Global Regulatory Affairs and Clinical Safety. Responsibilities: execute application build and configuration, manage solution lifecycle, develop and support data migration and scripts, troubleshoot issues, and ensure compliance through technical documentation. Collaborates with system architects, operations, and global stakeholders to deliver scalable, secure solutions aligned with regulatory requirements. Requirements: Bachelor's degree in Computer Science, Life Sciences, or related field; 5+ years in enterprise applications, with hands-on experience in Microsoft Power Platform, Dataverse, Power Apps, Power Automate, and solution lifecycle management. Preferred: experience supporting regulated pharma/biotech processes, Power BI, APIs, SharePoint, and enterprise support tools. High-Value: supporting pharmaceutical/regulatory data management systems, solution configuration, and compliance in a regulated, GxP environment. Work setup: hybrid with approximately 10% travel.