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HomeCompaniesNdd Medizintechnik AgJunior Design Quality Specialist (50-60%)

Junior Design Quality Specialist (50-60%)

Ndd Medizintechnik Ag · Zürich · Hybrid · Active · Personio

Job facts

FieldValue
CompanyNdd Medizintechnik Ag
TitleJunior Design Quality Specialist (50-60%)
Normalized title-
Department / teamQuality Services / Fix positions_Du-Form
LocationZürich
Work modelHybrid / Hybrid
Employment typePart Time
Salary-
Statusactive
ATS providerPersonio
Posted / first seen2026-04-22 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-20

Related slices

PageWhat it containsOpen
Company jobsActive postings from Ndd Medizintechnik Ag.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Personio.Open
Provider filtered searchThe same provider as a filtered job collection.Open
Department jobsActive postings in Quality Services.Open
Work model jobsActive Hybrid postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyNdd Medizintechnik Ag
Sourceebb0fd9c-609c-4de4-a1ff-db3d8f5a577d
ATS providerPersonio

Description

Tasks Labelling & Translations Drive labelling activities for assigned products in line with regulatory and market requirements. Coordinate translations of labels, operator manuals, and software-related texts. Ensure accuracy, consistency, version control, and timely implementation of updates. Perform verification activities to confirm compliance with defined requirements. UDI Management Manage UDI activities for assigned products, including assignment, maintenance, and database updates. Ensure alignment between UDI, labelling, and technical documentation. Support UDI-related changes across the product lifecycle. Quality & Compliance Support Support PMS and risk management activities, ensuring alignment with labelling and IFU content. Contribute to CAPA activities related to labelling, UDI, and product information. Maintain quality records and support audits as required. About the position Your key role is to support design quality activities and product integrity by coordinating labelling, translations, and UDI management. As a Junior Design Quality Specialist, you contribute to essential quality and regulatory processes, including Quality Management, Risk Management, Post-Market Surveillance, and CAPA. You support the creation, maintenance, and accuracy of compliant product documentation and ensure it remains up to date throughout the entire product lifecycle, in close collaboration with cross-functional teams. Do you want to help us to make lung function testing accessible to everyone everywhere, and to improve the lives of millions of people with lung diseases? Then you have come to the right place! Your profile Bachelor's degree in biomedical engineering, life science discipline or comparable technical or scientific field. 0-2 years of professional experience in quality management, design quality, regulatory affairs, or another regulated environment. Exposure to documentation, labelling, translations, or product development activities within the medical device industry is an advantage Experience supporting coordination with internal teams and external service providers, including basic task tracking and follow-up actions. Good communication and interpersonal skills, with the ability to collaborate effectively in cross-functional teams. Solid writing skills, with high attention to detail and accuracy when preparing and maintaining documentation. Good knowledge of relevant standards such as ISO 14971, IEC 62366, IEC 60601‑1. Very good user knowledge of documentation tools (e.g. MS Office, Polarion). Professional fluency in English and German; additional languages are a plus. Why us? We offer an attractive location, fair pay, good social benefits, flexible working hours, hybrid work, and the best conditions in which to do excellent work. This includes comprehensive onboarding, professional and modern technology, and a collegial and supportive working environment. We promote equal opportunities, diversity, and inclusion. If this profile describes you and you would like to work at a fast-growing company in a global environment, then we should meet. Apply directly and exclusively via our e-recruiting tool. The more we learn about you, the better. We look forward to receiving your complete application and reference letters. Your data will be treated confidentially and discreetly. Contact We kindly ask for direct applications only. Unsolicited dossiers from agencies will not be considered, and we decline all responsibility for any fees related to such submissions. [email protected]

Full job record

Job ID4729a66c8a49946c3dc3108c68d1703939c9b379
Org ID2c6d8380-a98d-43b1-9308-b59b4f691272
Source IDebb0fd9c-609c-4de4-a1ff-db3d8f5a577d
Board IDebb0fd9c-609c-4de4-a1ff-db3d8f5a577d
Providerpersonio
Provider Job Key2609889
TitleJunior Design Quality Specialist (50-60%)
Normalized Title
Statusactive
Activeyes
Location TextZürich
DepartmentQuality Services
TeamFix positions_Du-Form
Employment Typepart_time
Workplace Typehybrid
Remote Policyhybrid
CountryZürich
Region
City
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://ndd-medizintechnik-ag.jobs.personio.de/job/2609889?language=en
Apply URLhttps://ndd-medizintechnik-ag.jobs.personio.de/job/2609889?language=en
First Seen At2026-05-30 06:09:24Z
Last Seen At2026-06-20 07:48:20Z
Last Checked At2026-06-20 07:48:20Z
Last Changed At2026-05-30 06:09:24Z
Inactive At
Source Posted At2026-04-22 11:47:59Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=personio/board=ndd-medizintechnik-ag.de/date=2026-06-20/2026-06-20T07-48-19-644Z-8ca962e7cd561bb3a77d03a4b07fa0b20efa9f258d9d5f29cb859779e97d49aa.json
Event Fields
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  "last_changed_at": "2026-05-30T06:09:24.824Z",
  "active_status": "active"
}
Parsed Structured
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Extensions
{}
Native Structured
{
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  "name": "Junior Design Quality Specialist (50-60%)",
  "office": "Zürich",
  "keywords": [],
  "schedule": "part-time",
  "createdAt": "2026-04-22T11:47:59+00:00",
  "seniority": "entry-level",
  "department": "Quality Services",
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  "subcompany": "ndd Medizintechnik AG",
  "employmentType": "permanent",
  "jobDescriptions": [
    {
      "name": "Tasks",
      "value": "<u>Labelling & Translations </u><br><ul><li>Drive labelling activities for assigned products in line with regulatory and market requirements.</li><li>Coordinate translations of labels, operator manuals, and software-related texts.</li><li>Ensure accuracy, consistency, version control, and timely implementation of updates.</li><li>Perform verification activities to confirm compliance with defined requirements.</li></ul><br><u>UDI Management</u><br><ul><li>Manage UDI activities for assigned products, including assignment, maintenance, and database updates.</li><li>Ensure alignment between UDI, labelling, and technical documentation.</li><li>Support UDI-related changes across the product lifecycle.</li></ul><br><u>Quality & Compliance Support </u><br><ul><li>Support PMS and risk management activities, ensuring alignment with labelling and IFU content.</li><li>Contribute to CAPA activities related to labelling, UDI, and product information.</li><li>Maintain quality records and support audits as required.</li></ul>"
    },
    {
      "name": "About the position",
      "value": "Your key role is to support design quality activities and product integrity by coordinating labelling, translations, and UDI management. As a Junior Design Quality Specialist, you contribute to essential quality and regulatory processes, including Quality Management, Risk Management, Post-Market Surveillance, and CAPA. You support the creation, maintenance, and accuracy of compliant product documentation and ensure it remains up to date throughout the entire product lifecycle, in close collaboration with cross-functional teams. Do you want to help us to make lung function testing accessible to everyone everywhere, and to improve the lives of millions of people with lung diseases? Then you have come to the right place!"
    },
    {
      "name": "Your profile",
      "value": "<ul><li>Bachelor's degree in biomedical engineering, life science discipline or comparable technical or scientific field.</li><li>0-2 years of professional experience in quality management, design quality, regulatory affairs, or another regulated environment.</li><li>Exposure to documentation, labelling, translations, or product development activities within the medical device industry is an advantage</li><li>Experience supporting coordination with internal teams and external service providers, including basic task tracking and follow-up actions.</li><li>Good communication and interpersonal skills, with the ability to collaborate effectively in cross-functional teams.</li><li>Solid writing skills, with high attention to detail and accuracy when preparing and maintaining documentation.</li><li>Good knowledge of relevant standards such as ISO 14971, IEC 62366, IEC 60601‑1.</li><li>Very good user knowledge of documentation tools (e.g. MS Office, Polarion).</li><li>Professional fluency in English and German; additional languages are a plus.</li></ul>"
    },
    {
      "name": "Why us?",
      "value": "We offer an attractive location, fair pay, good social benefits, flexible working hours, hybrid work, and the best conditions in which to do excellent work. This includes comprehensive onboarding, professional and modern technology, and a collegial and supportive working environment. We promote equal opportunities, diversity, and inclusion.<br>If this profile describes you and you would like to work at a fast-growing company in a global environment, then we should meet. Apply directly and exclusively via our e-recruiting tool. The more we learn about you, the better. We look forward to receiving your complete application and reference letters. Your data will be treated confidentially and discreetly."
    },
    {
      "name": "Contact",
      "value": "<span style=\"color:rgb(32,32,32);font-family:Inter, '-apple-system', BlinkMacSystemFont, 'Segoe UI', Roboto, 'Helvetica Neue', 'Open Sans', 'system-ui', '-apple-system', 'Segoe UI', Roboto, Ubuntu, Cantarell, 'Noto Sans', sans-serif, 'Apple Color Emoji', 'Segoe UI Emoji';font-size:14px;font-style:normal;font-weight:400;text-transform:none;background-color:rgb(255,255,255);display:inline;\">We kindly ask for direct applications only. Unsolicited dossiers from agencies will not be considered, and we decline all responsibility for any fees related to such submissions.</span><br style=\"border:0px solid;margin:0px;color:rgb(32,32,32);font-family:Inter, '-apple-system', BlinkMacSystemFont, 'Segoe UI', Roboto, 'Helvetica Neue', 'Open Sans', 'system-ui', '-apple-system', 'Segoe UI', Roboto, Ubuntu, Cantarell, 'Noto Sans', sans-serif, 'Apple Color Emoji', 'Segoe UI Emoji';font-size:14px;font-style:normal;font-weight:400;text-transform:none;background-color:rgb(255,255,255);\"><span style=\"color:rgb(32,32,32);font-family:Inter, '-apple-system', BlinkMacSystemFont, 'Segoe UI', Roboto, 'Helvetica Neue', 'Open Sans', 'system-ui', '-apple-system', 'Segoe UI', Roboto, Ubuntu, Cantarell, 'Noto Sans', sans-serif, 'Apple Color Emoji', 'Segoe UI Emoji';font-size:14px;font-style:normal;font-weight:400;text-transform:none;background-color:rgb(255,255,255);display:inline;\"> </span><br><span style=\"color:rgb(32,32,32);font-family:Inter, '-apple-system', BlinkMacSystemFont, 'Segoe UI', Roboto, 'Helvetica Neue', 'Open Sans', 'system-ui', '-apple-system', 'Segoe UI', Roboto, Ubuntu, Cantarell, 'Noto Sans', sans-serif, 'Apple Color Emoji', 'Segoe UI Emoji';font-size:14px;font-style:normal;font-weight:400;text-transform:none;background-color:rgb(255,255,255);display:inline;\">[email protected]</span>"
    }
  ],
  "occupationCategory": "quality_assurance_and_saftey",
  "recruitingCategory": "Fix positions_Du-Form"
}
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