Associate Director, Regulatory Affairs - Power Platform Solutions Specialist

Merck; North Wales (Montgomery County); Sur place; USD 140 000 - 190 000; Plein temps

Avantages offerts par ce poste

Hybrid work

Travel opportunities (approx. 10%)

Résumé du poste

Scorpion Therapeutics is seeking an Associate Director, Regulatory Affairs – Power Platform Solutions Specialist to lead the configuration and optimization of the Microsoft Power Platform within Global Regulatory Affairs and Clinical Safety. The role emphasizes data migration, script development, and compliance documentation.

You will collaborate with system architects, operations, and global stakeholders to deliver scalable, secure regulatory solutions, with hybrid work and travel approximately

Qualifications

• Bachelor's degree in Computer Science, Life Sciences, or related field.
• 5+ years’ experience with enterprise applications and Microsoft Power Platform.
• Hands-on experience with Dataverse, Power Apps, Power Automate, and solution lifecycle management.

Responsabilités

• Execute application build and configuration for regulatory platforms.
• Manage solution lifecycle and data migration scripts.
• Troubleshoot issues and ensure compliance through technical documentation.
• Collaborate with system architects, operations, and global stakeholders to deliver scalable, secure solutions aligned with regulatory requirements.

Connaissances

Power Platform

Dataverse

Power Apps

Power Automate

Solution lifecycle

Regulatory compliance

Formation

Bachelor's degree in Computer Science/Life Sciences

Outils

Microsoft Power Platform

Dataverse

Power Apps

Power Automate

SharePoint

Description du poste

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.