Location: Minnetonka, Minnesota, USA (100% Onsite)
Locals Preferred
Experience: 3-5 years

Key Responsibilities
-Develop and manage project plans, budgets, schedules, and risk registers.
-Drive design and development of medical devices in compliance with regulatory standards.
-Collaborate with cross-functional teams (engineering, quality, regulatory) to ensure alignment and compliance.
-Oversee product testing, validation, and verification activities.
-Maintain accurate documentation to support regulatory submissions and product lifecycle management.
-Primary Focus: Advance alternate source projects to completion (currently 4 active projects).
-Collaboration: Work with internal teams and external suppliers to meet project goals.
Nature of Role:
-Approximately 70% project management
-Approximately 30% task coordination (tasks largely handled by other team members)
-Tools: Uses Microsoft Project for project management (familiarity preferred, not required).
-Background: Engineering background preferred; experience in any technical field will also be considered.
Work Style: Highly deadline-driven, capable of managing multiple ongoing initiatives.

Core Skills
-Project management
-Cross-functional collaboration
-Regulatory compliance
-Technical documentation
-Strong communication skills

Education & Experience
-Bachelor’s degree (other degrees acceptable with relevant experience).
-3-5 years of work experience.