88 Jobs für Quality Assurance in Österreich

Job-ID:
60609

Location:
Wien, AUT

Job Level:
Management

Category:
Quality

Employment Type:
Permanent position

Octapharma specializes in the development of highly pure pharmaceuticals made of human blood plasma. As part of a family-owned enterprise, Octapharma in Vienna is not only the largest production site, but also a successful research location of the Octapharma Group. Since our company continues to grow, we are now hiring for our team:

Your new challenges which will inspire you:

• Lead the Clinical Quality Assurance team, define tasks and responsibilities covered by the department, keep oversight on Clinical Quality Assurance tasks and responsibilities
• Ensure clinical trials are conducted following the respective regulations and guidelines
• Provide compliance advise to operational units
• Ensure compliance of clinical documents with regulations and guidelines
• Support preparation, conduct and follow up of regulatory inspections of clinical studies
• Act as interface between Octapharma's Corporate Quality Assurance function and global Clinical R&D

Your Profile That Will Convince Us

• Completed University degree in natural sciences, preferably medical or biosciences
• At least 5 years of working experience in the Pharmaceutical or CRO Industry, preferably in Clinical Operations
• Experience in Quality Management
• Excellent in English, German is a plus (written and oral)
• Willingness to travel up to 25%
• Strong problem-solving and analytical skills
• Excellent written and verbal communication as well as strong organizational skills

Our Attractive Benefits For You

• Wide range of tasks in an international setting, flexibility and personal responsibility
• Reliable employer with generous employee benefits and a salary customary in the market
• Familiar setting of a family-owned enterprise with benefits such as Do & Co staff restaurant, extraordinary staff events and many more:

Additional Information
The minimum gross wage according to the collective agreement (chemical industry) for your new job is EUR 5.598,85. We strive to adapt your salary to your range of tasks and to your profile, which is why we are ready to pay wages higher than collectively agreed.

We are looking forward to new, committed employees who join forces with us to promote our strong growth in order to keep enabling our patients to live a better life - because it is in our blood Is it in your blood too? We are looking forward to receiving your application via our online career portal.

Your Contact
Johanna Proksch

Octapharma Pharmazeutika Produktionsges.m.b.H.

Oberlaaer Straße 235, 1100 Wien,

T:

About Octapharma
Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide.

Apply now

Cytiva ist ein globaler Anbieter von Technologien sowie Dienstleistungen, die die Entwicklung und Herstellung von Therapeutika vorantreiben und beschleunigen. Unsere Kunden leisten einen großen Beitrag zur Erhöhung der Lebenserwartung. Dieser reicht von biologischer Grundlagenforschung bis hin zur Entwicklung innovativer Impfstoffe, neuartiger Medikamente sowie Zell- und Gentherapien.

Bei Cytiva haben Sie die Möglichkeit, sich selbst und das Unternehmen kontinuierlich weiterzuentwickeln - Sie arbeiten an bedeutenden Herausforderungen, mit Menschen, die sich füreinander, für unsere Kunden und ihre Patienten einsetzen. Mit Mitarbeitern in 40 Ländern ist Cytiva ein Unternehmen, in dem jeder Tag die Möglichkeit bietet zu lernen und zu wachsen – so können Sie Ihre Karriere vorantreiben und Ihre Fähigkeiten langfristig erweitern.

Cytiva ist eines von neun Danaher Life Sciences-Unternehmen. An unserem Produktionsstandort in Pasching mit ca. 200 Mitarbeitern produzieren wir Zellkulturmedien in flüssiger und pulverisierter Form für die biopharmazeutische Industrie.

Zur Verstärkung unseres QA QMS Teams suchen wir zum nächstmöglichen Eintritt eine*n
QA Spezialisten*in (m/f/d) (Vollzeit).
Die ausgeschriebene Stelle ist als Karenzvertretung vorgesehen.

Was Sie tun

• Vorbereitung, Betreuung und Nachbereitung von Kundenaudits und Zertifizierungsaudits und Unterstützung des Internen Audit-Managements. Durchführung von Gemba Walks/Quality Walks
• Review und Genehmigung von Qualifizierungsdokumenten/ Computersystemvalidierungen/Excel-Dateien-Validierungen/ für die Bereiche Produktion und Qualitätskontrolle. Koordination von Themen zur Datenintegrität und Durchführung von Audit-Trail-Reviews. Überprüfung und Genehmigung von Reinraumbüchern, Wartungsplänen und Shutdown Initiativen
• Dokumentenmanagement inklusive Sicherstellung, dass globale Anforderungen in lokale Arbeitsanweisungen implementiert werden. Koordination, Vorbereitung und Nachbereitung des Qualitätsmanagement-Reviews (QMR), Erstellung/Aktualisierung und Aufrechterhaltung des Standort-Qualitätsplans (SQP)
• Unterstützung bei der Weiterentwicklung und Aufrechterhaltung des Qualitätsmanagement-Systems.
• Systemunterstützung in Pasching einschließlich administrativer Aufgaben in Veeva Quality Docs und Veeva QMS; Schulung von Mitarbeitern in Best Practices für NC/ CAPA/ Complaints/ Investigations/ Effizienzprüfungen

Wer Sie sind

• Erfahrungen im Arbeiten in einem regulierten Umfeld, vorzugsweise ISO9001, ISO13485 und/oder GMP Bereich
• Ausbildung im Bereich Qualitätssicherung/-management und/oder naturwissenschaftlichem, technischem Bereich (z.B.: Fachhochschul- oder Universitätslehrgänge im Bereich Biologie, Biotechnologie, Medizintechnik oder ähnlichem)
• Ausgezeichnete MS-Office Kenntnisse
• Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift
• Eigenständig, mit strukturierter Arbeitsweise, Entscheidungsfreude und -fähigkeit; Ausgeprägte sozialkommunikative Kompetenzen

Was wir bieten

• Wir bringen Sinn und Herausforderung in die tägliche Arbeit
• Zahlreiche Benefits wie z.B. Öffi Ticket, Essens- und Fitnesskostenzuschuss, freiwillige Pensionskasse, Employee Assistace Program.
• Gute öffentliche Erreichbarkeit und kostenlose Parkplätze
• Kollegiales und wertschätzendes Betriebsklima sowie ein internationales Unternehmensumfeld in einer stark wachsenden und zukunftsträchtigen Branche
• Flexible Arbeitszeiten und Möglichkeiten zur beruflichen Weiterentwicklung

Das Gehalt für diese Stelle beträgt € 46.300,-- Jahresbrutto (Vollzeit). Wir bieten ein attraktives Gehalt mit Bereitschaft zur Überzahlung, abhängig von Ihrer Qualifikation und Berufserfahrung. Gerne legen wir die Details in einem persönlichen Gespräch mit Ihnen fest.

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit

Within our team you will test a web-based image analysis platform for cloud-based AI (Artificial Intelligence) analysis of retina scans. You can help us bring together the most advanced technologies in computer and medical sciences and prevent loss of eyesight in patients with retinal diseases.

YOUR NEW ROLE

As a QA Engineer, you'll play a vital role in ensuring the quality and reliability of our products. This position requires both manual and automation testing skills, with a strong emphasis on manual testing. You will work closely with developers, product managers, and other stakeholders to catch issues early, ensure product stability, and continuously improve our testing processes.

Your responsibilities will include:

• Test Case Design: Write, review, and maintain test cases to ensure our products meet the highest quality standards.
• Test Execution: Perform both manual (primary) and automated test cases to identify issues.
• Defect Reporting and Verification: Accurately document bugs and track them through to resolution.
• Test Data Preparation: Analyze, define, and generate realistic and relevant test data.

OUR TECHNOLOGY SET

• Python as the most used programming language in our backend
• React for single-page Web applications
• AWS as Cloud Computing Platform
• Playwright for test automation
• Atlassian Suite (Jira/Confluence), Xray for test case tracking and report
• Database Postgres

YOUR PROFILE

• Degree in Computer Science or a comparable qualification
• Minimum 3 years of experience in Software Testing, with at least one year focused on Test Automation.
• Prior experience with test automation tools such as Playwright or Cypress
• Structured and analytical work approach
• Ability to handle multiple tasks and projects simultaneously
• Knowledge of software QA methodologies, tools and processes
• Ability to collaborate with a wide group of stakeholders
• Experience analyzing and contributing to user stories and acceptance criteria

NICE TO HAVE

• Experience with API testing using tools like Postman
• Knowledge of Performance Testing
• Experience with Python

BENEFITS & GOODIES

• Free sweets & fruits as well as a fridge with beverages and coffee in the office
• Spontaneous table tennis, darts, drinks, movies after work in the office and periodically occurring team buildings events
• Flexible working hours for a healthy work-life balance with home office possibilities
• Opportunity to participate in conferences, trainings and education courses
• Location in center of Vienna with great commute around using public transport

You can expect a salary starting at EUR 42.224,00 per year (on full-time basis, 38,5 hours/week based on the collective agreement) with the willingness to overpay according to your qualification and responsibility.

Fits to your current situation?

Then apply now directly or by by e-mail to

This job posting will close once enough applications have been received, so don't hesitate to apply. We look forward to receiving your application - a letter of motivation along with your CV would be a strong plus.

Deine Aufgaben
In deiner Rolle als Quality Assurance Specialist bist du der Dreh- und Angelpunkt für die Fertigung im Bereich der Qualitätssicherung und gemeinsam mit den Führungskräften für die Qualität im Segment "Assembly" verantwortlich. Dabei verantwortest du die Koordination und Abarbeitung von Qualitätsabweichungen (Interne- Lieferanten- und Kundenreklamationen) und stellst mit deinen umfangreichen Methodenkenntnissen die Produkt- und Prozessqualität in deinem Wirkungsbereich sicher.

Konkret Bist Du Mit Folgenden Tätigkeiten Vertraut

• Erste Ansprechperson für Qualitätsthemen in der Fertigung und die QA-Mitarbeiter am Shopfloor
• Koordination aller qualitätsrelevanten Themen im Fertigungsbereich, sowie enge Zusammenarbeit mit verschiedenen Nahtstellen (Einkauf, Entwicklung, Fertigung, Qualitätsmanagement)
• Verantwortung für die Steuerung, Dokumentation und Eskalation von Non-Conformance Cases inkl. Ursachenanalyse, Maßnahmenverfolgung und Nachhaltigkeitschecks
• Erarbeitung und Weiterentwicklung von Qualitätsstandards sowie Teilnahme an Shopfloor-Meetings
• Koordination und Durchführung von Produkt- und Prozessaudits

Dein Profil

• Abgeschlossene technische Ausbildung (Lehre, HTL, Uni/FH)
• Weiterbildung im Bereich Qualitätsmanagement/Qualitätssicherung von Vorteil
• Berufserfahrung in der Qualitätssicherung, idealerweise im Fertigungsumfeld
• Selbstständige und lösungsorientierte Arbeitsweise
• Selbstsicheres Auftreten und kommunikationsstarke Persönlichkeit
• Sehr gute EDV-Kenntnisse
• Fließende Deutsch- und Englischkenntnisse

Wir Bieten

• Flexible Arbeitszeiten sowie Möglichkeit zum teilweisen Home-Office
• Betriebsrestaurant mit abwechslungsreicher und saisonaler Küche (Essenszuschuss)
• Parkplätze sowie Ladestationen für e-Autos
• Für die Anreise vom Wohnort zum Arbeitsplatz übernehmen wir die Kosten des Öffitickets
• Paten- & Bildungsprogramm
• Kinderland und Krabbelgruppe mit Ganzjahresbetreuung
• Firmenevents
• Sportangebot (Beachvolleyballplatz, Übernahme der Startgebühr bei div. Laufveranstaltungen, …)

Unsere Löhne und Gehälter liegen über dem Kollektivvertrag (KV) der Elektro- und Elektronikindustrie. Die KV-Mindestwerte betragen zwischen € 3.775,27 und € 4.862,95 - mit Bereitschaft zur Überzahlung. Die genaue Höhe hängt von deiner Qualifikation und Erfahrung ab. Wir gehören zu den besten Arbeitgebern Österreichs und bieten zahlreiche Benefits, ein familiäres Betriebsklima sowie spannende Entwicklungsmöglichkeiten.

Möchtest du Teil eines engagierten Teams werden und mit deiner Energie Besseres bewirken? Dann freut sich Valentina Flecker über deine aussagekräftige Onlinebewerbung.

Bearbeitung von Validierungen

Prüfplanverwaltung

Risikoanalysen (FMEA, HACCP)

RCA

Bearbeitung von Quality Agreements

Mitarbeit bei CI Projekten

Administration Dokumentenmanagement

Reklamationsbearbeitung

Durchführen von internen Auditd

At the University of Vienna, over 10,000 individuals work together on the major issues of the future. Around 7,500 of them are employed in research and teaching, with a further 2,900 working in administration and organisation. We are looking for a

Quality Assurance Specialist

177 Special Unit for Quality Assurance

Start date: | Hours: 20.00 | Classification: §54 VwGr. IVa

The Special Unit for Quality Assurance conducts evaluations of organisational units, study programmes, courses and researchers. It is responsible for quality checks in appointment and tenure track procedures and prepares analyses relevant for management using various instruments (in particular surveys and data analyses). The offices of the Ethics Commission and the Ombuds Office for the Assurance of Good Scientific Practice are also part of the unit.

Completed higher education degree (at least a Master's or equivalent

• )
  Relevant professional experience in university quality assuranc- e
  Very good knowledge of qualitative and quantitative social science method- s
  Independent, structured and solution-oriented approach to work, ability to work in a tea- m
  High level of analytical skill- s
  Proficiency in survey software (especially EVASYS- )
  Knowledge of social science software programmes (such as , MAXQDA, SPSS, R) and data science/AI tool- s
  Comprehensive knowledge of MS Office (Access, Excel, Outlook, PowerPoint, Word- )
  Business fluent in written and spoken English and Germa- n
  Willingness and ability to familiarise yourself with new areas of responsibilit- y

Designing and implementing quality assurance procedures (e.g. surveys, evaluations, reviews

• )
  Collecting, analysing and evaluating qualitative and quantitative data (e.g. conducting interviews and writing reports on the results- )
  Providing technical support for the EVASYS survey software, including interfaces to Moodle, u:space and DW- H
  Researching reviewer- s

Work-life balance: You have flexible working hours and can also work remotely, with mutual consent also part-time.

Inspiring working atmosphere: You are part of an dedicated team with a diverse university background in a relaxed working environment.

Good public transport connections: Your new workplace is easily accessible by public transport.

Internal further training: We offer you the opportunity to deepen your skills on an ongoing basis.

Fair salary: The basic salary of €3, full-time) increases if we can credit professional experience.

Equal opportunities for all: We welcome every additional/new personality to the team

With your CV and letter of motivation

Leaving Certificat- e
Further documents, if necessary- .
Via our job portal / Apply now-butto- n

If you have any questions regarding the content, please contact:

Michael Hofer

We look forward to welcoming new people to our team

The University of Vienna is committed to equal opportunities and diversity. We strive to increase the proportion of women in academic and general university staff, particularly in management positions, and therefore expressly encourage qualified women to apply. Women will be given preference if equally qualified.

University of Vienna. Space for personalities. Since 1365.

Job ID: 60609

Location:
Wien, AT

Job Level: Management

Job Category: Quality

Employment Type: Permanent position

Career Level:

Octapharma specializes in the development of highly pure pharmaceuticals made of human blood plasma. As part of a family-owned enterprise, Octapharma in Vienna is not only the largest production site, but also a successful research location of the Octapharma Group. Since our company continues to grow, we are now hiring for our team:

Your new challenges which will inspire you:

• Lead the Clinical Quality Assurance team, define tasks and responsibilities covered by the department, keep oversight on Clinical Quality Assurance tasks and responsibilities
• Ensure clinical trials are conducted following the respective regulations and guidelines
• Provide compliance advise to operational units
• Ensure compliance of clinical documents with regulations and guidelines
• Support preparation, conduct and follow up of regulatory inspections of clinical studies
• Act as interface between Octapharma's Corporate Quality Assurance function and global Clinical R&D

Your profile that will convince us:

• Completed University degree in natural sciences, preferably medical or biosciences
• At least 5 years of working experience in the Pharmaceutical or CRO Industry, preferably in Clinical Operations
• Experience in Quality Management
• Excellent in English, German is a plus (written and oral)
• Willingness to travel up to 25%
• Strong problem-solving and analytical skills
• Excellent written and verbal communication as well as strong organizational skills

Our attractive benefits for you:

• Wide range of tasks in an international setting, flexibility and personal responsibility
• Reliable employer with generous employee benefits and a salary customary in the market
• Familiar setting of a family-owned enterprise with benefits such as Do & Co staff restaurant, extraordinary staff events and many more:

Additional information:

The minimum gross wage according to the collective agreement (chemical industry) for your new job is EUR 5.598,85. We strive to adapt your salary to your range of tasks and to your profile, which is why we are ready to pay wages higher than collectively agreed.

We are looking forward to new, committed employees who join forces with us to promote our strong growth in order to keep enabling our patients to live a better life - because it is in our blood Is it in your blood too? We are looking forward to receiving your application via our online career portal.

Your contact:

Johanna Proksch

Octapharma Pharmazeutika Produktionsges.m.b.H.

Oberlaaer Straße 235, 1100 Wien,

T:

Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide.

Deine Aufgaben:

In deiner Rolle als Quality Assurance Specialist bist du der Dreh- und Angelpunkt für die Fertigung im Bereich der Qualitätssicherung und gemeinsam mit den Führungskräften für die Qualität im Segment "Assembly" verantwortlich. Dabei verantwortest du die Koordination und Abarbeitung von Qualitätsabweichungen (Interne- Lieferanten- und Kundenreklamationen) und stellst mit deinen umfangreichen Methodenkenntnissen die Produkt- und Prozessqualität in deinem Wirkungsbereich sicher.

Konkret bist du mit folgenden Tätigkeiten vertraut:

• Erste Ansprechperson für Qualitätsthemen in der Fertigung und die QA-Mitarbeiter am Shopfloor
• Koordination aller qualitätsrelevanten Themen im Fertigungsbereich, sowie enge Zusammenarbeit mit verschiedenen Nahtstellen (Einkauf, Entwicklung, Fertigung, Qualitätsmanagement)
• Verantwortung für die Steuerung, Dokumentation und Eskalation von Non-Conformance Cases inkl. Ursachenanalyse, Maßnahmenverfolgung und Nachhaltigkeitschecks
• Erarbeitung und Weiterentwicklung von Qualitätsstandards sowie Teilnahme an Shopfloor-Meetings
• Koordination und Durchführung von Produkt- und Prozessaudits

Dein Profil:

• Abgeschlossene technische Ausbildung (Lehre, HTL, Uni/FH)
• Weiterbildung im Bereich Qualitätsmanagement/Qualitätssicherung von Vorteil
• Berufserfahrung in der Qualitätssicherung, idealerweise im Fertigungsumfeld
• Selbstständige und lösungsorientierte Arbeitsweise
• Selbstsicheres Auftreten und kommunikationsstarke Persönlichkeit
• Sehr gute EDV-Kenntnisse
• Fließende Deutsch- und Englischkenntnisse

Wir bieten:

• Flexible Arbeitszeiten sowie Möglichkeit zum teilweisen Home-Office
• Betriebsrestaurant mit abwechslungsreicher und saisonaler Küche (Essenszuschuss)
• Parkplätze sowie Ladestationen für e-Autos
• Für die Anreise vom Wohnort zum Arbeitsplatz übernehmen wir die Kosten des Öffitickets
• Paten- & Bildungsprogramm
• Kinderland und Krabbelgruppe mit Ganzjahresbetreuung
• Firmenevents
• Sportangebot (Beachvolleyballplatz, Übernahme der Startgebühr bei div. Laufveranstaltungen, …)

Unsere Löhne und Gehälter liegen über dem Kollektivvertrag (KV) der Elektro- und Elektronikindustrie. Die KV-Mindestwerte betragen zwischen € 3.775,27 und € 4.862,95 - mit Bereitschaft zur Überzahlung. Die genaue Höhe hängt von deiner Qualifikation und Erfahrung ab. Wir gehören zu den besten Arbeitgebern Österreichs und bieten zahlreiche Benefits, ein familiäres Betriebsklima sowie spannende Entwicklungsmöglichkeiten.

Möchtest du Teil eines engagierten Teams werden und mit deiner Energie Besseres bewirken? Dann freut sich Valentina Flecker über deine aussagekräftige Onlinebewerbung.

Let's build a healthier future, together By combining our unique strengths, we are redefining healthcare through sustainable action and innovation. For a behind-the-scenes look, check out this video to see how we at Roche are making personalized health care a reality.

The mySugr GmbH was acquired by Roche in 2017 and our Vienna office is one of Roche's global sites. You will be located here, in the heart of Vienna, no matter if you work on a mySugr, Accu-Chek, navify or any other Roche product or solution. You can read more about the history of mySugr & Roche here.

Here's what we're looking for:
We are looking for a proactive
*Performance QA Engineer *
to take a leading role in shaping the quality and stability of our healthcare products. You are a technical expert who not only excels at identifying performance bottlenecks but also enjoys building the tools and frameworks to prevent them. As a key partner to our development, architecture, and infrastructure teams, you will champion performance best practices, mentor colleagues, and drive a culture of quality and continuous improvement.

*Your mission: *

• Technical design and development of Performance framework for large core product and functional components
• Conduct requirement and design analysis, and prepare specifications, test cases, and test data for functional, regression, automation, and performance testing
• Conduct product validation test execution, develop performance test plans and test strategies, report defects, and generate test reports
• Work closely with application development, architecture, and infrastructure teams to define success criteria for automation, performance testing, and application analysis initiatives
• Mentor team members on performance testing best practices and drive adoption of testing frameworks
• Conduct load, stress, and endurance testing to ensure system reliability under diverse conditions
• Contribute to a culture of innovation, quality, and continuous improvement within an Agile team

Essential skills for your mission:

• Experience in performance testing, ideally within a product-focused organization
• Proficiency in Java programming for test automation and scripting (hands-on expertise required)
• Expertise with performance testing tools such as JMeter, LoadRunner, Gatling, or similar
• Strong SQL skills for writing and optimizing database queries
• Experience in test case management, reporting, and using bug tracking systems such as Jira
• Exposure to Linux and SQL, and flexible to work on manual testing when needed
• Strong knowledge of enterprise application architecture and technologies, including databases, web, web services, and reporting
• Strong comprehension, analytical, and problem-solving skills
• Good interpersonal and communication skills, quick learner, and good troubleshooting capabilities

*Bonus skills: *

• Bachelor's degree in Computer Science, Informatics, life sciences, or equivalent work experience is required
• Master of Science (MS) degree in a relevant study area is preferred
• Experience working in a regulated environment of the healthcare, diagnostics, and/or pharmaceutical industry with Information Security and Computer System Validation (CSV)
• Experience testing business intelligence/analytics applications or software for multi-tenant enterprise SaaS applications is a big plus
• Knowledge of UI/UX testing and accessibility standards (e.g., WCAG) is a plus

In Austria, we have a legal obligation to disclose the minimum salary according to our collective agreement, which is gross EUR per month for this position. But Rest assured, we offer amazing competitive compensation packages which take into consideration current market trends, therefore you can expect a higher offer that reflects your experience level.

*Who we are and what we care about? *
We are committed to providing a healthy, equal and inclusive working environment for our employees to bring true relief to the patient We care about family friendly career paths, sustainability, a healthy lifestyle and the flexibility of a modern workplace. We maintain a culture of learning and sharing, as well as open and candid feedback. At every level, there are many opportunities to develop and grow - both professionally and personally.

As a healthcare pioneer committed to transforming the lives of billions of people around the globe, we push boundaries to redefine what is possible. We know that early, accurate diagnosis is essential to maintain health, prevent disease and help advance new, targeted treatments and potential cures for the world's most serious health problems. We have a passion for innovation and a profound commitment to make a lasting impact on society by continuing to improve the standard of care for humankind. Our culture inspires us to create healthcare that is sustainable, efficient and financially viable. Healthcare that is built on people's needs, strong data and clinical insights. Healthcare that saves lives.

Interested?
Great. We'd like to hear from you Just click that "Apply Now" button and send us your CV in English …. and anything else that you think might impress us.

Roche is an Equal Opportunity Employer.