דרושים Quality Analyst Student ב-Philips ב-Israel, Haifa

Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
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 .

Supply Chain Student

The Production Planner focuses on planning, coordinating and controlling raw materials, and sub assembly inventory in a timely and cost-efficient manner. Ensuring that the end products required are available at the lowest possible cost at the right time, in the right place and in the right quantity.

Job Responsibilities:

• Capacity and Resources analysis
• Supply Chain scenarios (What if simulation) & analysis
• Identifying and implementing advance planning methodologies and tools
• Manufacturing planning & coordination
• Interface with supply management, production and service departments

ou're the right fit if:

• Student towards B.Sc. in Industrial Engineering or other relevant degree
• GPA 80+
• At least 3 semesters before graduation
• Ability to work 3-4 days a week
• Excellent communication skills & multi-tasking ability

Onsite roles require full-time presence in the company’s facilities.Indicate if this role is an office/field/onsite role.
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Mechanical Engineering Student

The mechanical engineering student will support Mechanical Engineers in all mechanical
components & sub-components design within the DMS sub-system.
Starting from the initial design to the preliminary design, critical design, prototypes,
manufacturing transfer and full manufacturing support

Job Responsibilities:

Supporting Mechanical Engineers in:

• Mechanical design – 3D models, drawings, prototype manufacturing, and production transfer.

• Analysis, testing, troubleshooting and documenting of mechanical units/subsystems of small to medium scope.

• Development of modeling, simulation and analysis. Produces the design requirements and designs for DMS Mechanical.

• Trouble shooting of DMS mechanical problems. Ability to evaluate & define the design correction – when needed.

Education/Skills and Experience Requirements

• Currently a Mechanical Engineering student

• Grade average- 80+

• Good English skills

• Ability to work 18 hours per week and at lease 3 semesters till graduation

• Basic Knowledge in Mechanical Design

• Knowledge/ Experience in mechanical of one of the 3D CAD programs such as IDEAS, Creo/ProE etc.

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 .

Responsibilities:

• Provide ongoing support to the Head of Legal in managing day-to-day Legal Operations activities, including document management and project support

• Assist with corporate secretarial work, including maintaining records and supporting filings

• Assist with healthcare compliance processes, including preparing, coordinating signatures for, and filing

documentation required by internal compliance procedures

• Help maintain internal legal tools, trackers, and databases

• Prepare internal summaries, memos, presentations, and meeting minutes

• Assist in drafting commercial agreements under supervision

• Conduct legal research and case law searches in legal databases

• Help with internal process documentation and organization of legal resources

• Handle sensitive and confidential materials with discretion

Requirements:

• Second-year law student at an Israeli university

• At least 3 semesters remaining before graduation

• Minimum grade average of 80+

• Availability to work 2–3 days per week

• Proficient in written and spoken English

• Highly responsible, organized, and detail-oriented

• Able to work independently with a hands-on approac

Onsite roles require full-time presence in the company’s facilities.Indicate if this role is an office/field/onsite role.
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As an Operations Quality Team Manager, you will lead Q&R activities in the system plant as a PQE team manager. You will be responsible for driving product quality improvements by leveraging statistics and data analysis techniques to enhance processes. Your role will involve close collaboration with production, manufacturing engineering, and suppliers to ensure process control, quality assurance, effective failure analysis, and continuous improvement.

Your role:

• Provide clear vision and strategy for the PQE team, ensuring alignment with organizational quality goals.
• Build and develop the capabilities of the quality team, fostering a culture of continuous improvement and collaboration.
• Lead MRB activities, periodic quality reviews, and provide actionable insights.
• Lead “real-time” manufacturing line investigations, identify root causes of issues, and ensure the implementation of corrective actions through comprehensive reporting and follow-up.
• Implement and monitor production and process controls, including Process Validation (PV), Equipment Qualification (EQ), Control Plans, and pFMEA.
• Maintain compliance with ISO 13485, FDA regulations, and other relevant standards.
• Prepare for and support external audits (regulatory, customer) and perform internal pre-audits.
• Act as a liaison between R&D and Operations to ensure a smooth transition during NPI and change management And work closely with Production, Supply Chain, and Manufacturing Engineering to improve overall quality performance.

You're the right fit if you have:

• Bachelor's degree in engineering, production technology, science, quality assurance, mechanical engineering, or other related field.
• A minimum of 3 years of experience as a quality manager or in a similar role.
• A minimum of 5 years of experience as a product quality engineer
• In-depth knowledge of quality assurance methodologies, standards, and regulatory requirements (e.g., ISO 13485, FDA, MDR).
• Fluent in English, both written and verbal.

s

• Experience working in medical device, pharmaceutical
• Proficiency in statistical analysis tools (e.g., Minitab, JMP) and methods such as Six Sigma.
• Expertise in quality systems, CAPA management, and risk assessment.
• Familiarity with SAP or other ERP systems for quality tracking.
• Experience in NPI (New Product Introduction) and production readiness activities.
• Knowledge of advanced manufacturing processes, automation, and Industry 4.0 principles.

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the company’s facilities.
Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.Indicate if this role is an office/field/onsite 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 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 commitment to diversity and inclusion .

You are responsible for

• Compile and maintain regulatory documentation databases or systems
• Support cross functional teams with regulatory guidance
• Coordinate efforts associated with the preparation of regulatory documents or submissions
• Coordinate, prepare, or review regulatory submissions for domestic or international projects
• Provide technical review of data or reports that will be incorporated into regulatory submissions to assure scientific rigor, accuracy, and clarity of presentation

To succeed in this role, you’ll need a customer-first attitude and the following

• Student for M.Sc. in BiomedicalEngineering/ Life Sciences, orequivalent degree
• Grades – 80+
• At least 1.5 years left before graduation
• Ability to work at least 18 hours per week (not including Friday)
• Fluent in English
• Relevant experience and familiarity with medical device industry - an advantage

Our hybrid working model is defined in 3 ways:

Biomedical Engineering Student
Your role:

• Arranging and performing clinical evaluation projects, applications\algorithms tests, analyzing results and deriving relevant evidence for performance, safety and claims substantiations.
• Working closely with development teams, physicians and clinical scientists to develop strong study plans, and related tools (e.g. analysis and annotation tools).
• Supporting writing and maintenance of formal documentation for regulatory compliance.
• Supporting reviews and writing of scientific literature.
• Assisting clinical specialists during the process of developing concepts for new applications and perform ongoing improvements.
• Supporting investigation(s) of customer complaints.

You're the right fit if:

• Student towards B.Sc/M.Sc in applied mathematics/biomedical engineering or similar engineering degree with at least 2 years to graduation
• Experience as data scientist/algorithm engineer, with code writing/data software (e.g. Python/MATLAB and R-studio/SAS/SPSS/Minitab or equivalent) is an advantage
• Experience within a healthcare/regulatory/legal/highly regulated environment is an advantage
• Innovative thinking to solve complex problems
• Grade average - 80 +
• Availability for at least 18 hours work a week
• Excellent English

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 .