2027 Spring Co-op Global Quality - Commercial Specification Committee
Core
Build digital tools and automated workflows to review pharmaceutical specification packages (JoS) against regulatory guidance and compile regulatory intelligence for Bristol-Myers Squibb.
Role type
Junior IC data engineer (pharma regulatory)
Builds
Automated review tools, regulatory intelligence repositories, and administrative automation workflows
Domain
Pharmaceutical quality / Regulatory science
Deliverable
production ML models
Required skills
Python, data analysis, structured data pipelines, regulatory science principles, gap analysis
Preferred skills
AI-assisted document review, dashboard development, template automation
Technologies
Python, Excel, SharePoint, AI tools
Responsibilities
Develop logic for automated JoS package review tools; Analyze Health Authority query data to build knowledge repositories; Implement automated administrative processes and tracking dashboards; Pre-populate specification proposal templates
Seniority
Co-op / Intern