Senior Program Manager

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đŸ”„ 13 hours ago

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Logo of Fortive

Fortive

10,000+ employees

Founded 2016

🏱 Enterprise

⚕ Healthcare Insurance

💰 Post-IPO Equity on 2020-03

Enterprise ‱ Healthcare Insurance

Fortive is a global industrial technology company that specializes in delivering advanced healthcare solutions, intelligent operating solutions, and precision technologies. With a team of 18,000 employees, Fortive works on solving tough technical challenges, empowering safer, smarter, and more efficient industrial operations. The company emphasizes sustainability, integrity, and continuous improvement, striving for a future that's stronger, safer, and smarter. Fortive has been recognized as one of America's Most Responsible Companies, demonstrating its commitment to positive social and environmental impact.

📋 Description

‱ Lead high-impact medical device development programs across hardware, systems, and consumables from concept through commercialization. ‱ Align and lead cross-functional teams across Engineering, Quality, Regulatory, Operations, Marketing, and external partners. ‱ Develop and continuously refine integrated program plans, proactively managing scope, schedule, resources, dependencies, and critical path. ‱ Proactively identify, assess, and mitigate program risks, prioritizing actions based on business impact. ‱ Facilitate structured, data-driven problem solving for complex technical and organizational challenges. ‱ Ensure alignment of programs with evolving business priorities, customer needs, and applicable medical device regulatory requirements. ‱ Own executive-level communication, influence cross-functional alignment, resolve trade-offs, and maintain momentum across complex programs. ‱ Promote a collaborative, high-performance environment that encourages innovation and continuous improvement. ‱ Serve as a role model for program management excellence by sharing best practices and mentoring peers.

🎯 Requirements

‱ 6+ years of program management experience leading end-to-end product development and commercialization of regulated products. ‱ 4+ years in the Medical Device industry, including hands-on experience leading programs that resulted in FDA 510(k) clearance. ‱ Demonstrated ability to lead large, global, and interdependent programs in technical domains. ‱ Hands-on experience with process improvement and metrics, including use of tools like Jira, Confluence, and Fortive Business Systems (FBS). ‱ Track record of mentoring and developing high-performing project teams. ‱ Proven ability to coach, mentor, and elevate team performance in a PMO or cross-functional environment. ‱ Aspiration and readiness to take on formal people leadership within a PMO.

đŸ–ïž Benefits

‱ Health insurance ‱ 401(k) matching ‱ Paid time off ‱ Flexible working hours ‱ Professional development opportunities

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