Director, Program Management

Posted Yesterday
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Irvine, CA, USA
In-Office
159K-226K Annually
Expert/Leader
Healthtech • Pharmaceutical
The Role
Leads enterprise portfolio strategy, governance, budgeting, resource planning, risk management, and execution for regulated Cordella heart-failure management products. Oversees hardware, software, firmware, mobile, AI/ML, and cloud development from concept through commercialization. Ensures stage-gate, design-control, verification and validation compliance while coordinating cross-functional teams. Builds and mentors program managers, drives executive alignment, manages product launches, and improves organizational project-management maturity.
Summary Generated by Built In

Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

The Director, Program Management leads the strategic and operational oversight of all Cordella product-and-platform-related projects within the Edwards Implantable Heart Failure Management (IHFM) organization. This role ensures the effective deployment of project management methodologies across the product lifecycle-from concept through commercialization-while aligning with corporate strategy and regulatory requirements. This role ensures alignment with corporate objectives, regulatory standards, and market needs while optimizing resource allocation, budget utilization, and portfolio value.

How you will make an impact:

• Portfolio Strategy & Governance: Lead the development and execution of the enterprise-wide product portfolio strategy, for the Cordella system including the PAP sensor, implantation components, online Patient Management platforms, at-home monitoring accessories and apps. Establish governance frameworks for portfolio prioritization, investment decisions, and lifecycle management. Drive portfolio rationalization efforts to ensure alignment with strategic goals and market opportunities.

• Agile & Hybrid Program Management: Champion Agile methodologies for software, firmware, mobile, AI ML, and cloud-based application development. Integrate Agile practices with traditional stage-gate processes to support hybrid development models. Ensure sprint planning, backlog grooming, and iterative delivery align with regulatory and quality standards.

• Budget Management: Own the portfolio-level budget planning and forecasting process. Monitor and report on budget performance across all projects and programs. Partner with Finance to ensure accurate tracking of capital and operational expenditures.

• Resource Planning & Optimization: Lead resource capacity planning across the portfolio to ensure optimal allocation of talent and tools. Identify resource gaps and recommend hiring or outsourcing strategies. Implement tools and processes for real-time visibility into resource utilization.

• Program & Project Execution: Oversee execution of complex programs involving hardware, software, and systems integration. Ensure consistent application of stage-gate processes and design control procedures. Drive schedule management and ensure on-time delivery of milestones and product launches. Manage concurrent development cycles across multiple platforms and technologies.

• Risk Management: Lead proactive risk identification, assessment, and mitigation planning across the portfolio. Facilitate risk reviews and escalation processes to ensure timely resolution. Integrate risk management into stage-gate reviews and executive reporting.

• Verification & Validation (V&V) Oversight: Ensure robust planning and execution of V&V activities across all programs. Collaborate with Quality, Regulatory, and Engineering to align V&V with compliance and product performance requirements. Monitor V&V timelines and resource needs to avoid bottlenecks and delays.

• Cross Functional Leadership: Partner with R&D, Product Management, Regulatory, Clinical, Quality, Manufacturing, Supply Chain, and Commercial teams to ensure integrated portfolio planning and execution. Facilitate executive reviews, drive strategic decisions, and ensure alignment between product development, clinical evidence generation, and market needs.

• Innovation & Technology Integration: Partner with Data Science, AI/ML, and Engineering teams to integrate advanced analytics and intelligent features into product roadmaps. Support innovation pipelines and early-stage concept development through structured project intake and evaluation. Foster a culture of experimentation, rapid prototyping, and continuous learning.

• Team Leadership & Development: Build and lead a high-performing team of project and program managers. Drive accountability, innovation, and continuous improvement while overseeing staffing, budgets, succession planning, coaching, and talent development.

• Elevate BU maturity level specifically in the multiples areas of project management (e.g., governance, resource management and project management knowledge)

What you will need (required):

• Bachelor's Degree or equivalent in related field and direct experience in project and program management or equivalent work experience based on Edwards criteria.

• Hands on experience managing large to midsize projects and/or programs of increasing complexity

What else we look for (preferred):

• Master's Degree or equivalent in related field and 10 -12 years of direct experience in medical device product development, project and program management

• PMP, PfMP, SAFE Certified or equivalent

• Proven success in managing complex portfolios and launching regulated products

• Strong leadership skills and ability to influence change

• Demonstrated ability to direct teams and provide coaching and feedback, including responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relations

• Proven expertise in usage and implementation of project management systems

• Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives

• Deep understanding of medical device regulations and development processes. Experience within a regulated environment

• Deep understanding of Agile, hybrid, and stage-gate methodologies. Familiarity with AI/ML, cloud platforms, and digital health technologies

• Expertise in portfolio management tools and processes

• Strong financial, analytical, and resource planning skills. Ability to lead in a matrixed, global environment

• Expert understanding and knowledge of procedures while looking beyond existing methodologies and own discipline to define and resolve complex problems relevant to developing the strategy on enterprise-wide projects and charting the course of overall programs

• Expert in project and program management, including managing, guiding and mentoring project managers

• Excellent problem-solving, organizational, analytical and critical thinking skills

• Excellent understanding and work experience with project budgets and financial management

• Experience in facilitating change, including collaboration with management and executive stakeholders

• Ability to work with abstract ideas or situation and translate it into concrete plan and specific objectives

• Ability to interact with senior management, and others concerning matters of significance to the company

• Ability to develop relationships and leverage them to influence change

• Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.

For California, the base pay range for this position is $159,000 - $226,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience).  Applications will be accepted while this position is posted on our Careers website.  


Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

Skills Required

  • Bachelor's degree or equivalent in a related field, plus direct project and program management experience or equivalent work experience
  • Hands-on experience managing large to midsize projects or programs of increasing complexity
  • Master's degree or equivalent in a related field
  • 10–12 years of direct experience in medical device product development, project management, and program management
  • PMP, PfMP, SAFe certification, or equivalent
  • Success managing complex portfolios and launching regulated products
  • Strong leadership and change-influence skills
  • Experience directing teams, coaching employees, and handling hiring, termination, and employee relations
  • Expertise implementing and using project management systems
  • Excellent documentation, communication, negotiation, interpersonal, and relationship-management skills
  • Deep understanding of medical device regulations, development processes, and regulated environments
  • Deep understanding of Agile, hybrid, and stage-gate methodologies
  • Familiarity with AI/ML, cloud platforms, and digital health technologies
  • Expertise in portfolio management tools and processes
  • Strong financial, analytical, budget, and resource-planning skills in a matrixed global environment
  • Expert-level project and program management experience, including mentoring project managers
  • Experience facilitating organizational change and collaborating with executive stakeholders
  • Ability to translate abstract ideas into concrete plans and objectives
  • Ability to build relationships and influence significant company decisions
  • Ability to comply with company, environmental health and safety, and pollution-prevention requirements

Edwards Lifesciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Edwards Lifesciences and has not been reviewed or approved by Edwards Lifesciences.

  • Healthcare Strength Health coverage is considered strong, with multiple plan choices, HSA options, and fertility support, and the company highlights holistic well‑being programs.
  • Retirement Support A company 401(k) match and well‑regarded retirement offerings add clear long‑term value to total compensation.
  • Equity Value & Accessibility An Employee Stock Purchase Plan with a discount and look‑back feature makes equity ownership accessible and enhances the total rewards package.

Edwards Lifesciences Insights

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The Company
HQ: Irvine, CA
13,687 Employees
Year Founded: 1958

What We Do

Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today. Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives. Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life. For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms

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