Job Description Summary

We are the makers of possible

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Why Join Us?

A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place. 

Become a maker of possible with us!

We are offering more flexibility! This position can be either full time or part time based on need and individual agreement.

For the BD Quality team we are seeking a Quality Specialist who collaborates with the professional services teams and the internal software manufacturer functions based in Vienna.

Main responsibilities will include:

• Develop and continuously improve the validation services (GMP) for our pharmaceutical customers, working closely with the services teams (validation from the customer’s perspective)
• Actively contribute to product quality and safety on the manufacturer’s side as a member of the quality team (validation from the manufacturer’s perspective)
• Coordinate risk management with expert teams and enhance risk-based approaches in our Quality System
• Lead activities demonstrating validation of our infrastructure and software tools (internal validation)
• Perform supporting quality activities (for example CAPA, change control, PMS) as member of the Quality team

Preferred requirements:

• At least 3 years of experience in a quality role in medical device or pharmaceutical industry
• Competence and expertise in relevant areas, for example software validation, standards compliance (ISO 13485 or ISO 9001), writing and improving processes, risk management/analysis, participation in multiple GMP validation projects in different roles
• Experience and interest in establishing and planning cross-functional processes and workflows for medical device and pharmacy software
• Excellent analytical skills and ability to abstract, preciseness.
• Interest in working in the health care business and in a regulated environment
• Fluent in English, German and other languages are a plus

The minimum annual gross salary for this position is €44,450.- (full-time basis, in: 'ST1/Einstiegsstufe'). Based on individual skills and experience, we offer appropriate additional payment.

Click on apply if this sounds like you!

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

To learn more about BD visit: https://bd.com/careers

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Primary Work Location

AUT Vienna - Handelskai

Additional Locations

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