The Staff ALM Administrator’s primary objective is to support and coordinate data migration, configuration changes, implementation, and general management of Insulet’s Application Lifecycle Management (ALM) tool(s) within R&D
Job Summary
The Staff ALM Administrator’s primary objective is to support and coordinate data migration, configuration changes, implementation, and general management of Insulet’s Application Lifecycle Management (ALM) tool(s) within R&D.
Key responsibilities include data migration, system administration of Helix and Polarion ALM, configuration management, user management, training and support, documentation, integration, monitoring, reporting, and troubleshooting.
For U.S.-based positions only, the annual base salary range for this role is $119,600.00 - $179,375.00, with eligibility for incentive compensation and a comprehensive benefits package.
Matching Summary
The Staff ALM Administrator’s primary objective is to support and coordinate data migration, configuration changes, implementation, and general management of Insulet’s Application Lifecycle Management (ALM) tool(s) within R&D.
Salary
Base: $119,600.00 - $179,375.00; Bonus/Equity: May be eligible for incentive compensation; Benefits: Comprehensive benefits package including medical, dental, vision, 401(k) with match, PTO
Skills & Requirements
Must-have
Helix and Polarion ALM systems administration
ALM tool data migration
ALM system configuration management
ALM user and license management
ALM system troubleshooting
Nice-to-have
Collaboration under Quality Management System
Experience with custom dashboards and reporting
Integration of external tools into ALM
Key Requirements
8+ years of experience with R&D ALM systems
B.S. in Engineering or technical discipline
Experience managing collaboration under a QMS
Demonstrated expertise in product development and commercialization
Experience managing cross-functional project teams
Five (5) years of experience in regulated medical device industry
Experience with design and development processes in compliance with FDA 21 CFR part 820, ISO 13485, IEC 62304, or ISO 14971