Philips Program Manager Image Guided Therapy Devices SPOC 

United States, Minnesota 

800224126

Program Manager: Image Guided Therapy Devices, SPOCJob Description

This role requires strong leadership, project management, and communication skills, as well as the ability to collaborate effectively across various departments like ISC Engineering, Commodities, and stakeholders. The Program Manager, SPOC will oversee the funnel building, planning, execution, and monitoring of cross functional R&D BU projects to ensure successful implementation and alignment with business goals.

Project Planning and Execution:Leading planning, execution, and monitoring of transformational projects. Define project scope, objectives, timelines, and resource requirements to ensure efficiency and budget adherence.

Stakeholder Engagement:Liaison with key stakeholders to gain buy-in & align, support for transformational initiatives and manage escalations.

Risk Management:Identifying potential risks and developing mitigation strategies.

Continuous Improvement:Identifying opportunities to streamline processes and optimize resources.

Performance Monitoring and Reporting:Establish KPIs and metrics to measure project progress.

-Experience:15+ years of extensive program management experience, ideally within the medical device or healthcare sector. Familiarity with regulatory compliance standards for medical devices, encompassing FDA regulations, ISO standards, and other pertinent guidelines.

-Education:Bachelor’s Degree in engineering, biomedical engineering, healthcare management, business administration, or a related field. Master's Degree, MBA, or advanced certification in project/program management is often preferred.

-Project and Program Management Skills:Proficiency in project and program management methodologies, such as PMI (Project Management Institute) standards, Agile, Scrum, and Waterfall.

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Technical Knowledge:

• In-depth understanding of medical device technologies, including design, development, manufacturing processes, and regulatory pathways for market approval.

• Familiarity with healthcare standards and regulations, including HIPAA (Health Insurance Portability and Accountability Act) and GDPR (General Data Protection Regulation).

• Knowledge of healthcare IT systems, electronic medical records (EMR), and interoperability standards.

-Regulatory Compliance and Quality Assurance:Knowledge of regulatory requirements and quality assurance standards applicable to medical devices, including FDA regulations, ISO 13485, and Good Manufacturing Practices (GMP). Experience in developing and implementing quality management systems (QMS)

You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.

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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion .

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