Senior Director, Program Management

🔥 0 minutes ago

🏄 California, Illinois, +3 more states – Remote

🏄 California – Remote 🌽 Illinois – Remote 🍂 Massachusetts – Remote ❄️ Minnesota – Remote 🤠 Texas – Remote

💵 $169.6k - $233.2k / year

⏰ Full Time

🟠 Senior

📋 Program Manager

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Siemens Healthineers

WebsiteLinkedInAll Job Openings

10,000+ employees

⚕️ Healthcare Insurance

🧬 Biotechnology

💰 $1.5M Grant on 2021-05

Healthcare Insurance • Biotechnology • Medical Device

Siemens Healthineers is a leading MedTech company focused on pioneering breakthroughs in healthcare. They offer a comprehensive portfolio that addresses the entire care continuum for serious diseases, including medical imaging, laboratory diagnostics, point-of-care testing, and digital health solutions. With a commitment to innovation, sustainability, and improving patient access to care, Siemens Healthineers collaborates with healthcare professionals and organizations globally to advance medical technology and enhance patient outcomes.

📋 Description

• Lead the execution of strategic Systems and Informatics product development programs within the Core Laboratory Solutions business. • Provide cross-functional leadership across R&D, Marketing, Quality, Regulatory Affairs, Manufacturing, Supply Chain, Service, and Operations to successfully develop and commercialize innovative laboratory diagnostic solutions. • Drive predictable execution across complex, global product development programs while balancing business objectives, technical risk, quality, schedule, and cost. • Manage substantial program budgets while leading global cross-functional teams, external development partners, suppliers, and OEMs. • Lead executive program governance by providing clear communication of program health, key milestones, risks, mitigation plans, dependencies, and critical decisions to Integrated Business Planning (IBP) governance teams and senior leadership. • Ensure successful completion of all Product Delivery Excellence (PDx) phase gate requirements while driving consistent execution and continuous improvement across programs. • Identify, assess, and proactively manage technical, regulatory, operational, and business risks throughout the product lifecycle. • Build strong partnerships across global organizations while influencing without direct authority to achieve enterprise objectives. • Drive a culture of accountability, transparency, collaboration, and disciplined execution across cross-functional teams.

🎯 Requirements

• Extensive experience leading complex, integrated medical device product development programs involving hardware, software, automation, systems integration, and laboratory diagnostic solutions within a regulated environment. • Demonstrated success leading multidisciplinary R&D teams through all phases of product development, verification, validation, regulatory approval, commercialization, and sustaining engineering. • Proven ability to align program execution with business strategy while maintaining a strong product value proposition. • Experience leading global cross-functional teams across R&D, Marketing, Quality, Regulatory Affairs, Manufacturing, Supply Chain, Service, and Operations. • Strong knowledge of medical device product development processes, Design Controls, risk management, and FDA and international regulatory requirements. • Demonstrated ability to proactively identify program constraints, evaluate technical and business trade-offs, and drive timely executive decisions. • Excellent leadership, communication, negotiation, and influencing skills with the ability to build alignment across diverse global organizations. • Experience managing third-party development partners, strategic suppliers, and OEM relationships.

🏖️ Benefits

• medical insurance • dental insurance • vision insurance • 401(k) retirement plan • life insurance • long-term and short-term disability insurance • paid parking/public transportation • paid time off • paid sick and safe time