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Program Manager: Image Guided Therapy Devices, SPOC
3 months ago
The Program Manager (SPOC) will be responsible for leading and managing strategic initiatives aimed at driving organizational goals (BOM productivity savings, Margin Improvements, etc.) and achieving business objectives
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.
The SPOC role in internal business development (Class III medical device) is essential for promoting collaboration, alignment, and efficiency across the organization's various functions and departments. By serving as an independent Single Point Of Contact, the SPOC helps streamline processes, optimize resources, and drive successful outcomes of BoM productivity savings in achieving business goals and objectives.
Your role:
Leading global cross functional teams for assigned BoM Productivity Savings funnel building projects:
Strategy Development: Collaborating with senior leadership to define strategic objectives for SPOC. Developing plans and roadmaps for productivity savings, supply assurance, supplier transfers, and margin improvement.
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.
Centralized Communication: Acting as the Single Point Of Contact for all internal stakeholders involved in business initiatives. Like, ISC Engg Team, Procurement, Commodities, IGTD BU R&D, SQE etc.
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.
You will be a part of a high-impact, global organization within Philips that works across all modalities – The Sustaining Engineering Team (STET).
STET has been established as an entrepreneurial organization that focuses on fast-paced, high-quality portfolio transfers within the Philips global supply base to mitigate risk & maximize profitability.
You're the right fit if:
- You've acquired 15+ years of extensive program management experience, ideally within the medical device or healthcare sector, and familiarity with regulatory compliance standards for medical devices, encompassing FDA regulations, ISO standards, and other pertinent guidelines.
- Your skills include project and program management: Proficiency in project and program management methodologies, such as PMI (Project Management Institute) standards, Agile, Scrum, and Waterfall.
- You have a 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.
- You have the following 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. Knowledge of regulatory requirements and quality assurance standards applicable to medical devices, including FDA regulations, ISO13485, and Good Manufacturing Practices (GMP). Experience in developing and implementing quality management systems (QMS)
- You have proven leadership abilities to inspire and motivate cross-functional teams, foster collaboration, and drive accountability for program deliverables.
- You're an excellent communicator and have people skills to engage with diverse stakeholders, including executives, project teams, vendors, regulatory agencies, and end-users
- You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.
About Philips
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.
- Learn more about our business.
- Discover our rich and exciting history.
- Learn more about our purpose.
- Read more about our employee benefits.
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 here.
Additional Information
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Plymouth, MN.
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This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.
Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.