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Quality MDR (Medical Device Regulation) Intern

Philips

Quality MDR (Medical Device Regulation) Intern

full-timePosted: Jan 13, 2026

Job Description

Job Title

Quality MDR (Medical Device Regulation) Intern

Job Description

oin our Quality MDR (Medical Device Regulation) team and gain valuable experience in the medical device industry, supporting regulatory compliance processes. As an intern, you will play a key role in assisting the team with document verification, data analysis, and supplier communication, all while learning about EU and FDA medical device regulations.

Your role:

  • Verify supplier documentation to ensure compliance with medical regulations.

  • Assist with data extraction & analysis in Excel.

  • Review and interpret documents and email correspondence for accuracy.

  • Work within SAP and other internal systems to manage documentation.

You’re the right fit if:

  • You are a student in at least 2nd year of Bachelor studies.

  • You are detail-oriented with strong analytical abilities.

  • You are proficient in using MS Office package, especially Microsoft Excel.

  • You are a quick learner with the ability to recognize patterns and adapt to new tasks.

  • You are fluent in English and Polish.

  • You are available to work at least 25 hours/week

How we work together

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.

What We Offer:

  • A 6-month internship based on a civil contract with competitive salary.

  • Flexible working hours that can be adapted to your university schedule.

  • The opportunity to use English in your daily activities.

  • Access to learning platforms like LinkedIn Learning and Philips University.

  • A chance to build your career within an international company known for innovation.

  • Discount for the multisport card.

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.

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-Office

Locations

  • Lodz, Lódzkie, Poland

Salary

Estimated Salary Rangemedium confidence

25,000 - 45,000 EUR / yearly

Source: ai estimated

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

Skills Required

  • detail-orientedintermediate
  • strong analytical abilitiesintermediate
  • proficient in MS Office (especially Excel)intermediate
  • quick learnerintermediate
  • ability to recognize patternsintermediate
  • adapt to new tasksintermediate
  • fluent in English and Polishintermediate

Required Qualifications

  • student in at least 2nd year of Bachelor studies (experience)
  • available to work at least 25 hours/week (experience)

Responsibilities

  • Verify supplier documentation for compliance with medical regulations
  • Assist with data extraction & analysis in Excel
  • Review and interpret documents and email correspondence for accuracy
  • Work within SAP and other internal systems to manage documentation

Benefits

  • general: 6-month internship on civil contract
  • general: competitive salary
  • general: flexible working hours adapted to university schedule
  • general: opportunity to use English daily
  • general: access to LinkedIn Learning and Philips University
  • general: chance to build career in international company
  • general: discount for multisport card

Target Your Resume for "Quality MDR (Medical Device Regulation) Intern" , Philips

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Tags & Categories

detail-orientedstrong analytical abilitiesproficient in MS Office (especially Excel)quick learnerability to recognize patternsadapt to new tasksfluent in English and PolishHealthcare Technology
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Philips logo

Quality MDR (Medical Device Regulation) Intern

Philips

Quality MDR (Medical Device Regulation) Intern

full-timePosted: Jan 13, 2026

Job Description

Job Title

Quality MDR (Medical Device Regulation) Intern

Job Description

oin our Quality MDR (Medical Device Regulation) team and gain valuable experience in the medical device industry, supporting regulatory compliance processes. As an intern, you will play a key role in assisting the team with document verification, data analysis, and supplier communication, all while learning about EU and FDA medical device regulations.

Your role:

  • Verify supplier documentation to ensure compliance with medical regulations.

  • Assist with data extraction & analysis in Excel.

  • Review and interpret documents and email correspondence for accuracy.

  • Work within SAP and other internal systems to manage documentation.

You’re the right fit if:

  • You are a student in at least 2nd year of Bachelor studies.

  • You are detail-oriented with strong analytical abilities.

  • You are proficient in using MS Office package, especially Microsoft Excel.

  • You are a quick learner with the ability to recognize patterns and adapt to new tasks.

  • You are fluent in English and Polish.

  • You are available to work at least 25 hours/week

How we work together

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.

What We Offer:

  • A 6-month internship based on a civil contract with competitive salary.

  • Flexible working hours that can be adapted to your university schedule.

  • The opportunity to use English in your daily activities.

  • Access to learning platforms like LinkedIn Learning and Philips University.

  • A chance to build your career within an international company known for innovation.

  • Discount for the multisport card.

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.

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-Office

Locations

  • Lodz, Lódzkie, Poland

Salary

Estimated Salary Rangemedium confidence

25,000 - 45,000 EUR / yearly

Source: ai estimated

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

Skills Required

  • detail-orientedintermediate
  • strong analytical abilitiesintermediate
  • proficient in MS Office (especially Excel)intermediate
  • quick learnerintermediate
  • ability to recognize patternsintermediate
  • adapt to new tasksintermediate
  • fluent in English and Polishintermediate

Required Qualifications

  • student in at least 2nd year of Bachelor studies (experience)
  • available to work at least 25 hours/week (experience)

Responsibilities

  • Verify supplier documentation for compliance with medical regulations
  • Assist with data extraction & analysis in Excel
  • Review and interpret documents and email correspondence for accuracy
  • Work within SAP and other internal systems to manage documentation

Benefits

  • general: 6-month internship on civil contract
  • general: competitive salary
  • general: flexible working hours adapted to university schedule
  • general: opportunity to use English daily
  • general: access to LinkedIn Learning and Philips University
  • general: chance to build career in international company
  • general: discount for multisport card

Target Your Resume for "Quality MDR (Medical Device Regulation) Intern" , Philips

Get personalized recommendations to optimize your resume specifically for Quality MDR (Medical Device Regulation) Intern. Takes only 15 seconds!

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

Check Your ATS Score for "Quality MDR (Medical Device Regulation) Intern" , 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

detail-orientedstrong analytical abilitiesproficient in MS Office (especially Excel)quick learnerability to recognize patternsadapt to new tasksfluent in English and PolishHealthcare Technology
Quiz Challenge

Answer 10 quick questions to check your fit for Quality MDR (Medical Device Regulation) Intern @ Philips.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.