Related skills
project management cross-functional collaboration qms regulatory compliance pdm📋 Description
- Lead cross-functional medical device programs from concept to launch
- Build integrated program plans, schedules, and deliverables
- Drive milestone tracking, dependencies, and blockers
- Facilitate core team meetings, design reviews, and executive updates
- Identify critical paths and proactively manage risks
- Partner with Quality and Regulatory for verification, validation, and regulatory submissions
🎯 Requirements
- BS in Engineering, Science, or related field
- 5+ years of program or project management in medical devices
- Design controls and phase-gate development knowledge
- Verification and validation experience
- Comfortable across R&D, Quality, Regulatory, Ops, and external vendors
- Excellent written and verbal communication
🎁 Benefits
- Hybrid onsite work arrangement
- Robust benefits package
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