דרושים Verification Test Equipment Engineer ב-Philips ב-United States, Bothell

In this role, you will have the opportunity to actively participate in global projects, making improvements, providing best in class services and directly contributing to the success of Philips on a daily basis. You will be responsible for Daily support for SLM (Supplier Lifecycle Management) users regarding the process, SAP Ariba tool and other tools supporting the process in terms of the usage and reporting functionality.
Your role:

• Daily support for SLM users regarding the process, SAP Ariba tool and other tools supporting the process in terms of the usage and reporting functionality

• User Management

• Conducting training sessions for users (e.g. buyers, procurement engineers, commodity managers)

• Maintenance of reports/reporting dashboards

• Database maintenance

• User materials maintenance

• Resolving daily technical issues related to tools supporting the process

You're the right fit if:

• You have a University degree in Business Administration or Management, Supply Chain Management, Data Analysis and Analytics or equivalent

• You are interested in working in an international environment in the Procurement area

• You have good intuition in escalating beyond instructions

• You have an excellent interpersonal and communication skills

• You have good time management skills and ability to multi-task and prioritize work

• You have flexible working attitude given the different time-zones of the customers, within respected limits of CET-time-zone

• You have MS office applications skills (Outlook, Excel)

• You are fluent in English

• You are engaged, motivated, ambitious, eager to learn and develop new skills and knowledge

• Understanding of basic database maintenance will be an advantage

• Experience in the field of SAP support would be an asset

Our benefits:

• Employment contract

• Hybrid way of working (3 days per week at office in Lodz)

• Support in relocation

• Annual bonus based on performance achieved

• Private medical care with the option to extend it to family members

• Benefit System cards

• Discount for Philips’ products

• Wide variety of training & learning opportunities

• Promotion of a healthy lifestyle in the office

• Employee Assistance Program

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 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 culture of impact with care .

System Integration Engineer - Medical Device Hardware (Bothell, WA)

You will contribute to the development and release of best-in-class Ultrasound innovations influencing the practice of medicine around the world. You will work with Electrical/Mechanical Hardware, Software, and Ultrasound Acoustic Engineering development teams to ensure product functionality, performance, and customer quality is achieved.

Your role:

• As a member of the systems engineering development team, you will coordinate, influence, and implement test and integration planning in support of new ultrasound features and new product releases.

• You will own project integration and product reliability test strategies to ensure the successful development and deployment of Ultrasound product development projects.

• This technical leadership position will involve individual project deliverables and project status reporting as well as coordination of technical.

• This role includes engagement with the multi-disciplinary engineering team; electrical hardware, mechanical hardware, software, and ultrasound physics/acoustics development teams.

• Responsible for developing and extending organization approaches and strategies in Systems Engineering/Integration practices.

You're the right fit if:

• You have 5+ years in electrical/electromechanical development experience with a focus on Systems Engineering and product integration and testing in FDA Regulated (ISO 13485) Medical Device product development (other highly regulated environments could be considered).

• You’re an experienced technologist with a background in on or more of the following (Displays, PC chipsets, graphics cards, high speed signal processing, power supply). You have the ability to analyze, troubleshoot, and solve complex technical problems.

• You've earned a BS in Electrical Engineering, Computer 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 .

• You have strong individual technical leadership skills through strategy definition and mentorship as well as strong interpersonal and communication skills with the ability to interface in a cross-disciplinary manner, including engineers, product managers, and clinical specialists.

How we work together:

This is an office-based 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.

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The pay range for this position in WA is $110,000 to $177,000.

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 .

Clinical Marketing Manager, IGT-S APAC

As a Clinical marketing manager, you will work on the implementation and execution of a strong market readiness, be involved with downstream marketing activities and content development, provide inputs into product development, and partner with key internal stakeholders to support their go to market initiatives. In addition, involvement in clinical validation activities, claims generation and the regulatory submission process for new product introduction. Accountable for IGT-S customer visits, KOL and reference site management, participate in international tradeshows, and proof point collection with your strong clinical knowledge, hands-on expertise in IGT-S.

1. Your role:

• Drives clinical programs to support market readiness and post-market growth initiatives.
• Support downstream marketing functions with image collection, that highlights our IGT-S solution proof points, whilst ensuring patient and data privacy (this is in coordination with IGT-S clinical application specialists)
• Support marketing strategy, roadmap implementation, providing inputs relating to workflow, quantification and imaging performance.
• Contributes to the global and regional KOL/reference site management, speaker pool, and peer-to-peer market activities (in collaborate with clinical scientist).
• In coordination with IGT-S application specialist, builds and maintains a competitive clinical content database (e.g., clinical images and case) aligned with product value propositions.
• Collaborates cross-functionally across internal teams and global markets to drive clinical adoption and knowledge sharing.
• Provides training to empower clinical experts and enhance customer engagement.
• Deliver customer product demonstrations during congress/tradeshow

2. You're the right fit if:

Education

• Bachelor's/Master's Degree in medical related field, Healthcare Administration and/or equivalent.

Work Experience

• Minimum 5 years of experience with Masters/Bachelor's in areas in Medicine, Healthcare Technology, Product Management, Medical Technology, Medical Sales, Clinical Marketing or equivalent.

Preferred Qualifications

• At least 10 years of experience in a medical field, experience in Interventional procedures is a plus.
• Good knowledge of the cathlab technology and familiarities with other imaging modalities (CT, MR, US)
• Good clinical knowledge allowing to understand customer needs and value drivers in the healthcare imaging domain and more specifically minimally invasive interventional procedures
• Boldness to support market readiness and expansion whenever possible, exploiting Philips technologies, market positions and brand
• Ability to synthesize market and customer feedback into insights helping clinical adoption
• Good organization skills especially in supporting marketing events.
• Ability to deliver in a complex environment (high-end technology, highly professional customers, and global scope) to meet demanding business targets
• Strong communication skills and ability to lead a multi-functional and global team to contribute to market readiness and market expansion. Ability to relate and communicate with different levels and functions in the organization

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 the lives of others.
• Learn more about .
• Discover .
• Learn more about .
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 culture of impact with care .

In this role you

The Product Quality Engineer is accountable for oversight of system and hardware quality and risk management throughout the product life cycle.

Your role:

• Ensures that appropriate quality plans are made that include all stages of the lifecycle of the product and supports Quality plan design
• Validates key design inputs for usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability and costs
• Provides effective oversight of the execution of the Quality Plan, any Risk Management activities, and of all design related activities during the product/system lifecycle
• Performs independent technical assessment on product quality performance and post-market product quality analysis. Can Lead quality related problem solving and root cause analysis during design and manufacturing
• Creates and uses post-market analytics, statistics and deliverables to report on product quality performance in the field (provide feedback to manufacturing, suppliers or design teams) and initiates field actions when required

You're the right fit if:

• 2+ years of Design Quality Engineering experience in a regulated environment, preferably within Medical Device.
• Bachelor’s degree in a scientific discipline, Engineering preferred or equivalent.
• 2+ years of experience in Assessing quality plans and product designs, reviewing test and other performance data, Analyses of market feedback, Leading root cause analysis and quality problem solving.
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.

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
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• Learn more about

The pay range for this position in Bothell, WA is $82,650 to $140,000, Annually.

.

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.

within commuting distance to Bothell WA.

Verification Test Equipment Engineer (Bothell, WA)

This is an exciting opportunity to join the Oral Healthcare team as a Verification Test Equipment Engineer, contributing to the development of next-generation Sonicare products. In this fast-paced role, you will support Systems Engineering and the Test & Verification Lab by ensuring that product testing equipment is designed, maintained, and optimized to effectively verify that products meet stringent design requirements. Your work will be critical in enabling robust product testing and analysis to deliver world-class oral health innovations.

Your role:

• You will be responsible for keeping assembly, measurement, and test equipment in a product development laboratory environment in optimal condition.
• Assist project engineers and lab technicians in troubleshooting a broad range of custom developed assembly and test equipment.
• Collaborate with product development project teams to improve test methods, recommend, and implement improvements to test equipment, and adapt test equipment to newly developed products.
• Create calibration and maintenance procedures and work instruction and perform scheduled calibration and preventive maintenance to automated and semi-automated test equipment (custom developed and off-the-shelf).
• Follow all regulations, safety guidelines, and equipment operating/maintenance procedures to meet specific requirements.
• Manage inventory of spare parts, consumables, and tools necessary to support installed equipment.

You're the right fit if:

• You’ve acquired 5+ years of experience inthe field of test and verification within product development is preferred. Experience related to the development and testing of medical (FDA regulated) products is a plus. (ISO 13485, 21CFR820).
• Your skills includeHands on experience with pneumatic actuators and systems, sensors, measurement systems, and vision systems. LabVIEW, Matlab or Python programming experience a plus.
• You have aBachelor’s degree in Mechatronics/Electrical/Electronics/Mechanical Engineering or equivalent professional engineering experience.
• You are willing to travel occasionally in support of new equipment development projects.
• You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
• You have an

How we work together

(This is an on-site 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 $110,000 to $177,000

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.

• Creates and executes comprehensive process validation strategies using statistical tools to ensure seamless transition of new products to production, meeting quality and regulatory standards, working under limited supervision.
• Handles the entire design control process, from eliciting and validating design inputs to managing verification, validation, and smooth design transfer, ensuring rigorous adherence to regulatory and quality standards.
• Keeps a check on the drafting and updating of detailed quality engineering documents, including quality plans for hardware, software, and systems, ensuring all documentation is accurate, up-to-date, and compliant with regulatory requirements.
• Ensures success of quality improvement projects by integrating quality, reliability, and Post Market Surveillance (PMS) insights into all stages of the product lifecycle, driving continuous enhancement of product quality and reliability.
• Conducts thorough assessments of product and system designs, reviews performance data, and performs root cause analysis to identify and address quality deficiencies, ensuring the highest standards of design excellence.
• Validates critical design inputs such as usability, reliability, performance, manufacturability, and safety, ensuring alignment with both quality standards and regulatory requirements.
• Guides comprehensive risk management activities throughout the product lifecycle, ensuring potential risks are accurately identified, assessed, and effectively mitigated to uphold product safety and quality.
• Leverages post-market performance data to assess product effectiveness in the field, providing actionable feedback to manufacturing and design teams, and initiating corrective actions when necessary.
• Ensures preparation for quality audits and inspections, maintaining all necessary documentation and processes to demonstrate compliance with both internal and external quality standards.
• Records, manages, and executes CAPA processes, including problem identification, root cause analysis, and implementation of solutions to prevent recurrence and drive continuous improvement.
• Applies continuous improvement techniques to enhance quality practices, ensuring ongoing audit readiness and strict adherence to both internal and external quality standards throughout the product lifecycle.
• Builds effective relationships with internal and external stakeholders, providing guidance and mentorship to ensure alignment with quality standards and project milestones.

Bachelor's / Master's Degree in Mechanical Engineering, Electronics Engineering, Science or equivalent.
Minimum required Experience:

Minimum 2 years of experience with Bachelor's in areas such as Quality Engineering, Safety Engineering, R&D Engineering or equivalent OR no prior experience required with Master's Degree.

Six Sigma Green Belt
• Design Quality Management
• Data Analysis & Interpretation
• Design for Quality (DFQ)
• Root Cause Analysis (RCA)
• CAPA Methodologies
• Regulatory Requirements
• Privacy, Safety and Security Risk Assessment
• Technical Documentation
• Continuous Improvement
• Product Quality and Reliability
• Defect Management
• Design Verification Planning
• Design Validation Planning
• Product Test Design

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 the lives of others.
• Learn more about .
• Discover .
• Learn more about .
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 culture of impact with care .

Your role:

• Developing and adapting MR pulse sequences to provide improvements in image quality or new clinical contrasts
• Investigating root causes of customer complaints
• Contributing to regulatory clearance of new products
• Maintaining connections with other groups within Philips as well as external customers, to share knowledge in new applications of MR physics
• Contributing to invention disclosures

You're the right fit if:

• Masters or PhD in Physics, Mathematics, or MR related science
• A minimum of 3 years of experience in MRI
• In-depth understanding of MR physics and experience with pulse sequence software
• Affinity with programming in C++ and/or Python, with an interest in creating high quality software
• Proven innovation ability (e.g. patents, journal papers)
• Fluency in English
• Experience working with multidisciplinary teams
• Creative and innovative with a willingness to take risks in order to create advanced concepts through fast prototyping, and able to engineer these prototypes into solid product designs

Onsite roles require full-time presence in the company’s facilities.
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