Global Leader Emergency Care jobs at Philips in United States, Bothell

• Provides enterprise architecture guidance to IT Architects, facilitates strategic decision-making, and supports the development and implementation of cohesive architectural solutions across the enterprise.
• Spearheads the assessment of current and future capabilities, identifying opportunities for improvement and takes charge of Business Capability Analysis, ensuring that IT strategies align seamlessly with overarching business, market, and financial objectives.
• Leads enterprise architecture roadmap activities, communicates with stakeholders regarding developments and milestones, and the maintains Enterprise Architecture (EA) assets to ensure its alignment with evolving technology landscapes.
• Manages enterprise architecture risk, mitigates potential issues, and collaborates with stakeholders to maintain the integrity and security of the architecture framework across the organization.
• Facilitates enterprise architecture communication, ensures clear and effective information exchange among stakeholders, and promotes collaboration across teams to optimize resource utilization and enhance overall operational efficiency.
• Drives comprehensive enterprise-wide architecture integration acrossProduct andEnterprise IT and ensures cohesive alignment, streamlined processes, and optimal resource utilization throughout the organization's technological landscape.
• Guides and mentors other enterprise IT architects to ensure the effective execution of their work, foster skill development and adherence to organizational standards.
• Leads the delivery of the multi-year enterprise architecture roadmap by providing critical input into the yearly planning cycle, ensures resource allocation, and the seamless integration of long-term architectural goals with annual objectives.

• Bachelor's / Master's Degree in Information Technology, Computer Science, Enterprise Architecture Frameworks, Cloud Architecture, Data Architecture, Agile and DevOps Practices or equivalent.
• Minimum 8 years of experience in IT Solution Design, Business Process Management, Enterprise Architecture, Cloud Architecture or equivalent.
• TOGAF (The Open Group Architecture Framework) certification (preferred)
• Self-motivated, with an ability to work under own initiative, often under time criticalconditions
• Can-do, problem-solvingattitude
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
• Your experience includes medical device or heath technology industries, including compliance with FDA, ISO, and other regulatory requirements.
• Strong experience with digital transformation and change management initiatives.
• Proven ability to bridge the gap between business needs and technical solutions.
• Strong stakeholder engagement, communication, and presentation skills.
• You thrive in cross-functional teams and are comfortable operating within a global, matrixed organization.

• Learn more about .
• Discover
• Learn more about
• Learn more about

As a,,

Your role:

• Lead global product launches and drive the adoption of GI & WH products and solutions.
• Partner with regional teams to optimize Go-To-Market.
• Collaborate with upstream product management, clinical, and research teams to ensure success in the marketplace.
• Oversee product launch readiness and ensure smooth new product introductions.
• Drive demand generation through branding, campaigns, and sales enablement efforts.

You're the right fit if:

• You have a Bachelor’s Degree. MBA preferred.
• You have 5+ years of experience in marketing, or product management. Ultrasound experience required.
• Your skills include excellent communication, presentation, and interpersonal and influence skills at all levels of an organization. As well as a collaborative mindset to work cross-functionally, up and downstream, to design the successful activation plans our value propositions in the regions.
• field. Experience studying and living abroad preferred.
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
• You are an adaptable, open-minded team player with a can-do mentality, able to identify opportunities within business challenges and turn them into actionable plans that drive cross-functional team execution.

How we work together

This is an office role.

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 .
• Discover
• Learn more about
• Learn more about

The pay range for this position in Bothell, WA is $126,000 to $202,000.

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.

We expect the transaction to close at the end of 2025. With Bridgefield’s support and building on our 40+ year legacy of growth and innovation in emergency medical technology, the Emergency Care business will continue passionately pursuing our mission of saving lives, lowering the cost of healthcare, and advancing the science of resuscitation while serving the public access AED, EMS, military, and hospital market segments.

Your Role:

• Provide oversight and leadership of assigned complaint handling and regulatory reporting organizations. Foster a team culture where team members feel valued, listened to, encouraged to grow, and try new things.
• Drive effective preparation for audits and timely resolution to all audit non-conformances including internal and external. When necessary, partner with legal manufacturing sites, Philips compliance team, and trusted partners to support creation/submission/closure of responses to FDA/Competent Authority observations to ensure a positive outcome for Philips. Communicate with the FDA and other regulators, as needed.
• Ensure robust dashboards/performance management reports are maintained for each complaint handling organization and that CAPAs are owned/driven to closure with urgency, high quality investigations, with root cause and corrective actions in place. Provide visibility to management and escalation management and resolution, when necessary.
• Collaborate with leadership in Quality, Medical Affairs, R&D, Service, Manufacturing, OEMs, among others, to ensure timely escalations of critical complaints, and investigations are thorough and timely. Work cross-functionally and in collaboration with other senior leaders within the business and with outsourcing partners develop and lead transformations, performance management and strategic roadmap. Engage with business units on upcoming product launches and ensure resources are budgeted and in place.
• Member of the Quality Leadership team and support strategic plans/objectives for the Global Complaint Management Organization, as well as developing strategic changes needed to ensure timely & accurate complaints investigation and closure, including on-time regulatory reporting globally.

You're the right fit if:

• You’ve acquired a minimum of 10+ years’ experience in FDA regulated quality/regulatory environments, with a focus on Post Market Surveillance / Complaint Handling / Regulatory Reporting / Quality Operations and a minimum of 4 years’ experience leading/managing teams in a fast paced, high visibility environment. Product experience with AED’s/Defibrillators or other Class III Devices containing medical electrical equipment/software highly desired.
• You have proven leadership experience delivering on strategic commitments and transformation across various aspects of Quality, with experience in Business/Organizational separations/divestitures highly preferred.
• You've demonstrated a collaborative customer focus; with high performance behavior of shared accountability, listening and learning, sense of urgency, entrepreneurial, trust and influence management, self-growth, empowerment, and continuous improvement.
• You have prior FDA and other regulatory audits/inspections experience is required. Experience corresponding to regulatory inquiries associated with regulatory device reporting (i.e. MDR, MDV, etc.) is required
• You have extensive experience/knowledge of most regulations relative to Post Market Surveillance activities and reporting, such as: ISO 9001/13485/14971, FDA Regulations (21CFR (803, 806, 820, etc.)), MDSAP, JPAL, Medical Devices Directive (93/42/eec, 98/79/EC)), and EU MDR.
• You have a minimum of a Bachelor’s degree in Quality, Engineering, or equivalent
• 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.

• Learn more about .
• Discover
• Learn more about
• Learn more about

Philips Transparency Details:

• The pay range for this position in Bothell, WA is $172,200 to $275,520.

• 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 Bothell, WA.
• May require travel up to 20%.

• Develop and maintain a customer solution portfolio strategy that supports EC’s strategic plan. This includes leading, developing, and managing product management teams across EC’s product segments and geographies. Imperative to this responsibility is systematically collecting and analyzing customer, clinical, and competitive insights to guide commercial strategies and product development roadmaps
• Lead global Marketing E-Commerce activities (i.e. Brand Management, Insights & Analytics, Integrated Communications, Events and Digital Marketing E-Commerce), including ensuring consistency with EC’s new company brand identity.
• Drive brand preference and reputation to position the business in the market consistent with the objectives of the strategic plan.
• Enable increased sales force effectiveness by leading development of solution selling strategies, building and deploying sales and partner tools, designing effective marketing assets, and managing EC’s global tradeshow and conference presence.

• You’ve acquired 15+ years of experience in… marketing, sales, and business development leadership roles in pre-hospital, emergency med tech, medical informatics, and/or AED market segments.
• Your skills include…. Experience leading both upstream and downstream Marketing teams, including in med tech businesses serving global customer bases with partner-centric go-to-market models
• You have a Master’s degree in business and/or marketing
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
• You’re an… Experienced leader of med tech sales teams and indirect channel strategies.

• Learn more about .
• Discover
• Learn more about
• Learn more about

Reporting to the National Sales Manager - IGT, you will be instrumental in developing and managing numerous business strategies to achieve profitable business relationships across our IGT (fixed systems, mobile surgery and hemo-dynamics portfolio). Your Capital Equipment / Medical Device sales experience coupled with your ability to influence at all levels will be key to your success in the role.

Your challenge

• Achieving and growing sales in your territory and assisting in advancing revenue and market position consistent with company goals
• Achieving solid account penetration, manage and growing new and existing accounts
• Developing and managing key customer relationships.
• Deliver clinical, technical and sales support to customers in collaboration with the business unit and applications team
• Developing and executing professional education workshops/events for new and experienced customers in collaboration with the business unit and applications team
• Delivers persuasive and informative presentations to senior customer audiences, effectively communicating complex solutions to support high-impact sales activities
• Maintaining up to date CRM and sales tools and providing regular updates to the National Sales Manager and key stakeholders

You’re the right fit if:

• Experience in healthcare sales and strategy, ideally within image guided therapies, capital equipment or medical devices
• Exceptional understanding of the sales processes with the ability to protect and grow market share
• High levels of motivation, energy and a drive to achieve results
• Excellent communication skills combined with the ability to build strong internal and external networks
• Ability to deliver persuasive presentations to senior customer audiences
• Experience in building and executing a strategy for targeted accounts

Your role:

• Leads and directs all aspects of Global quality operations/assurance program activities, including Emergency Care business separation/divestiture quality transformation, including strategy design/development, execution oversight, independent assessment, and compliance by design initiatives, compliance management, and capability building, to ensure adherence to quality standards and continuous improvement across the organization.
• Will contribute to strategic planning involving mission, vision, and policies to ensure alignment and effectiveness in organizational decision-making and adaptability.
• Supports supplier/3rd party qualification, audits, and assessment process, supports external/internal audits, aids in regulatory compliance gap closure, operational quality metrics, agreements, and records, and participates in operational quality-related communication and feedback.
• Develops and executes requirements, conditions, and enablers within the Emergency Care business and ensures that all products released adhere to pertinent safety and environmental regulations, guaranteeing compliance and upholding standards.
• Leads planning, staffing, budgeting, expense management prioritization, and drive proposals and implementations of methodological changes to ensure organizational efficiency and effectiveness.
• Establishes a supply chain quality assurance practice at the delivery model level, oversees and ensures the performance of teamwork within the defined scope per delivery model, and maintains responsibility for regulatory compliance of Emergency Care sites within their jurisdiction.
• Manages and monitors quality compliance issues and conflict resolution and leads cross-functional discussions to determine adequate resolutions that support business needs.
• Supports product recall procedures, ensures swift and efficient resolution in accordance with company policies and regulatory standards, and oversees all aspects of the recall process to maintain compliance and uphold consumer safety.
• Acts as the senior-level manager, possesses broad expertise and unique knowledge, shapes company objectives and principles, contributes creatively and effectively towards goal attainment, and is recognized as an expert both within the company and the industry.

You're the right fit if:

• You’ve acquired a minimum of 10 years’ experience in Quality Operations/Supply Chain Assurance within FDA regulated (ISO 13485) medical device environments. Product experience with AED’s/Defibrillators or other Class III Devices containing medical electrical equipment/software highly desired.
• You have proven experience leading global Quality Operations/Supply Chain Assurance programs and transformational initiatives, with experience in Business/Organizational separations/divestitures highly preferred.
• You’ve acquired extensive experience and knowledge of global medical device regulations, guidance, and applicable standards including ISO 14971, ISO 13485, 21CFR 820, EU MDR.
• You have a proven track record of working/communicating effectively with Global cross-functional teams and with internal/external stakeholders (e.g. Notified Bodies, FDA, Competent Authorities).
• You have a Minimum of a Bachelor’s Degree (Required) in a Quality discipline, Supply Chain Management, Engineering, Clinical/Life Science or similar disciplines. Master’s Degree desired. ASQ Certifications desired.
• 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.

• Learn more about .
• Discover
• Learn more about
• Learn more about

Philips Transparency Details:

• The pay range for this position in Bothell, WA is $172,000 to $275,000.

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 Bothell, WA.
• May require travel up to 40%.

• Focal point of contact between business/region/function leadership and global IT and process owning roles for any IT related concerns.
• Stakeholder engagement with leadership in a business/region(zone)/function to define their IT strategy (per Group IT strategy) in alignment with strategic business objectives.
• Participate in the strategic planning process with assigned business/region/function to understand priorities and relate to available or required IT enablers; represent the assigned scope in global (IT) programs and roadmaps to ensure fit for purpose.
• Drive qualification and quantification of business/region/function requirements, also by courageous conversations. Align/converge towards consolidated planning of prioritized investments, which are resourced-to-win in business and IT.
• Joint effort with the broader community in exploration & execution of initiatives.
• Oversee all programs with impact on (or in interest of) own business/region/function and possibly directly lead or coach IT streams and dependencies in their execution, deliver through IT platforms incl drive related business readiness.
• Collaborate with business/region/function owners for continuous improvement of IT enabled processes incl high quality data as well as change management for adoption and adherence in the business community.
• Evaluate IT landscape of assigned business/region/function scope and develop migration paths for consolidation & continuous improvement as part of IT strategy.
• Provide insights of new technology developments and advice on how this can impact/contribute the business strategy.
• Collaborate with involved leaders in business/region/function & IT for business continuity incl. escalation management and mitigated business impact.

• Years of experience (15+) in IT transformation roles desirably in similar/Health Tech industry
• Prior experience in managing IT in a M&A environment, particularly with separations or divestitures
• Previous project management experience, preferably in leading IT projects.
• Technical understanding of various IT systems, infrastructure, and software.
  • Specific knowledge/experience of med device IT landscapes, operating procedures and compliance – especially with regard to IT CSV (computer system validation) and related FDA regulations for computerized systems.
  • Experience managing IT suppliers (including off shore), IT supplier / software contracts and license management.

• 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.