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Supplier Quality Engineer 3

Philips

Supplier Quality Engineer 3

full-timePosted: Jan 13, 2026

Job Description

Job Title

Supplier Quality Engineer 3

Job Description

Senior Supplier Quality Engineer
Implement Quality Engineering, Purchasing Controls and Supplier Quality processes related to the development, procurement and continuous improvement of manufacturing materials, components, software, sub-assemblies, contract manufactured finished devices/products or services, and their introduction into Philips supply chain.

Your role:

  • Completes Qualification of raw material and components (including spare parts), development/ improvement of supplier processes, supplier process control plans; ensuring that the supplied part meets specifications, and the control limits/tolerances for parameters are met. 

  • Qualifies and sustains sub- processes of suppliers, including performing process validations for critical supplier processes impacting part quality. 

  • Ensures that the components/products at the supplier (including spare parts and services) are released according to agreed specification and quality requirements (APQP / PPAP) and Supplier Quality audit results.

  • Executes SCAR management, effective and timely closure.

  • Execute Non-Conformances evaluation regarding to raw material.

  • Lead or participate in the audit assessment of supplier ensuring they are compliant with associated policies/procedures and GMPs requirements.

  • Independently produces and completes Supplier Quality Engineering related activities and documentation.

You're the right fit if:

  • Bachelor’s degree in an engineering or a combination of equivalent job experience in related field, 3-5 years in medical industry in areas related to Quality Assurance, Incoming Quality, or Complaints.

  • Advance English level.

  • Knowledge in: problem solving with quality tools such as: 6 sigmas, 8-D, CAPA, 5WHYs.Knowledge of Good Manufacturing Practices and ISO 13485. CAPA system, as well global medical device regulation standards such as: 21 CFR parts 803, 806, and 820, ISO13485, ISO14971, European Medical Device Directive. Root cause analysis, corrective and preventive action methods. Product/quality development methods: CtQ definition, DfSS, SPC, APQP, FMEA, control plans.

  • Experience auditing supplier is desirable.


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 the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.

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.

#LI-PH1 

Locations

  • Alajuela, Alajuela, Costa Rica

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 EUR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • problem solving (6 sigma, 8-D, CAPA, 5WHYs)intermediate
  • Good Manufacturing Practicesintermediate
  • ISO 13485intermediate
  • global medical device regulations (21 CFR 803,806,820, ISO14971)intermediate

Required Qualifications

  • Bachelor’s degree in engineering or equivalent (experience)
  • 3-5 years in medical industry in Quality Assurance, Incoming Quality, or Complaints (experience)
  • Advanced English level (experience)

Responsibilities

  • Qualify raw materials and components
  • Develop/improve supplier processes and control plans
  • Qualify and sustain supplier sub-processes
  • Ensure components meet specifications (APQP/PPAP)
  • Execute SCAR management
  • Evaluate Non-Conformances
  • Lead/participate in supplier audits

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Tags & Categories

problem solving (6 sigma, 8-D, CAPA, 5WHYs)Good Manufacturing PracticesISO 13485global medical device regulations (21 CFR 803,806,820, ISO14971)Healthcare Technology
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Answer 10 quick questions to check your fit for Supplier Quality Engineer 3 @ Philips.

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Philips logo

Supplier Quality Engineer 3

Philips

Supplier Quality Engineer 3

full-timePosted: Jan 13, 2026

Job Description

Job Title

Supplier Quality Engineer 3

Job Description

Senior Supplier Quality Engineer
Implement Quality Engineering, Purchasing Controls and Supplier Quality processes related to the development, procurement and continuous improvement of manufacturing materials, components, software, sub-assemblies, contract manufactured finished devices/products or services, and their introduction into Philips supply chain.

Your role:

  • Completes Qualification of raw material and components (including spare parts), development/ improvement of supplier processes, supplier process control plans; ensuring that the supplied part meets specifications, and the control limits/tolerances for parameters are met. 

  • Qualifies and sustains sub- processes of suppliers, including performing process validations for critical supplier processes impacting part quality. 

  • Ensures that the components/products at the supplier (including spare parts and services) are released according to agreed specification and quality requirements (APQP / PPAP) and Supplier Quality audit results.

  • Executes SCAR management, effective and timely closure.

  • Execute Non-Conformances evaluation regarding to raw material.

  • Lead or participate in the audit assessment of supplier ensuring they are compliant with associated policies/procedures and GMPs requirements.

  • Independently produces and completes Supplier Quality Engineering related activities and documentation.

You're the right fit if:

  • Bachelor’s degree in an engineering or a combination of equivalent job experience in related field, 3-5 years in medical industry in areas related to Quality Assurance, Incoming Quality, or Complaints.

  • Advance English level.

  • Knowledge in: problem solving with quality tools such as: 6 sigmas, 8-D, CAPA, 5WHYs.Knowledge of Good Manufacturing Practices and ISO 13485. CAPA system, as well global medical device regulation standards such as: 21 CFR parts 803, 806, and 820, ISO13485, ISO14971, European Medical Device Directive. Root cause analysis, corrective and preventive action methods. Product/quality development methods: CtQ definition, DfSS, SPC, APQP, FMEA, control plans.

  • Experience auditing supplier is desirable.


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 the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.

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.

#LI-PH1 

Locations

  • Alajuela, Alajuela, Costa Rica

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 EUR / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • problem solving (6 sigma, 8-D, CAPA, 5WHYs)intermediate
  • Good Manufacturing Practicesintermediate
  • ISO 13485intermediate
  • global medical device regulations (21 CFR 803,806,820, ISO14971)intermediate

Required Qualifications

  • Bachelor’s degree in engineering or equivalent (experience)
  • 3-5 years in medical industry in Quality Assurance, Incoming Quality, or Complaints (experience)
  • Advanced English level (experience)

Responsibilities

  • Qualify raw materials and components
  • Develop/improve supplier processes and control plans
  • Qualify and sustain supplier sub-processes
  • Ensure components meet specifications (APQP/PPAP)
  • Execute SCAR management
  • Evaluate Non-Conformances
  • Lead/participate in supplier audits

Target Your Resume for "Supplier Quality Engineer 3" , Philips

Get personalized recommendations to optimize your resume specifically for Supplier Quality Engineer 3. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Supplier Quality Engineer 3" , Philips

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

problem solving (6 sigma, 8-D, CAPA, 5WHYs)Good Manufacturing PracticesISO 13485global medical device regulations (21 CFR 803,806,820, ISO14971)Healthcare Technology
Quiz Challenge

Answer 10 quick questions to check your fit for Supplier Quality Engineer 3 @ Philips.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.