Senior Medical Product & Project Manager — Global Impact

Minimed; Los Angeles (CA); On-site; USD 124,000 - 212,000; Full time

Job summary

MiniMed is seeking a passionate Configuration Management professional to join our team in Northridge, CA. You will lead cross-functional initiatives to plan, develop, and sustain products and processes, ensuring precise BOM control and smooth transfer to manufacturing while aligning with regulatory expectations.

This full-time on-site role requires strong collaboration, meticulous requirements management, and the ability to drive issues to resolution across global projects.

Qualifications

• Bachelor’s degree with 4+ years of relevant experience; advanced degree with 2+ years is also acceptable.
• Experience leading cross-functional teams and coordinating multi-disciplinary programs.
• Ability to translate complex requirements into actionable plans and drive them to successful delivery.

Responsibilities

• Leads cross-functional teams to evaluate, develop and manage projects for new product development and lifecycle management of products and processes.
• Oversees operational aspects of projects and serves as liaison between project management and line management.
• Manages development and implementation processes of products and services across departments.
• Reviews project status, manages schedules and prepares status reports.
• Monitors projects from initiation through delivery and intervenes when needed.
• Gathers requirements and ensures stakeholder needs are met through planning and elicitation.
• Owns BOM and change orders for transfer to manufacturing sites.
• Travel 15-20% domestically and internationally.

Skills

Medical device regs

Detail oriented

Problem solving

Education

Bachelor’s degree

Advanced degree

Job description

MiniMed is seeking a passionate Configuration Management professional to join our team in Northridge, CA. You will lead cross-functional initiatives to plan, develop, and sustain products and processes, ensuring precise BOM control and smooth transfer to manufacturing while aligning with regulatory expectations.

This full-time on-site role requires strong collaboration, meticulous requirements management, and the ability to drive issues to resolution across global projects.