Senior Design Quality Engineer

vor 3 Wochen


Hamburg, Deutschland Abbott Vollzeit

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health.We’re always looking towards the future, anticipating changes in medical science and technology. 

In Germany, Abbott has more than 4,000 employees working in manufacturing, research and development, logistics, manufacturing,sales and marketing. They are located at Abbott`s German headquarters in Wiesbaden and its sites in Hanover, Neustadt am Rübenberge, Wetzlar, Eschborn, Cologne, Jena and Hamburg. 

Working at Abbott

At Abbott, you can do work that matters and help people to live a healthier and full life, grow your career, and learn, be your true self. You will have access to: 

Career development with an international company where you can grow the career you dream of

An attractive benefits package (e.g.attractive Abbott Pension Plan , a company bike, employee stock purchase program)

A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. 

A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. 

A challenging position in a fast-growing crisis independent industry

To become part of a dynamic, highly educated, highly skilled, and motivated team

Flat hierarchies, open appreciative mentality, and efficient, constructive lines of communication

Multi-national environment, where we foster the development of our talents within the enterprise

Join Our Team in Abbott Automation Solutions GmbH as a Design Quality Engineer (Software focus) (m/f/d), based in Hamburg

Are you passionate about ensuring the safety and effectiveness of medical devices? We’re looking for a talented Design Quality Engineer with a software focus to join our dynamic team and make a real difference in people’s lives

What You’ll Do:

Drive Innovation: Oversee design control processes for on-market and in-development medical devices, ensuring they meet the highest standards of safety and effectiveness. Collaborate for Success: Work closely with software developers, product managers, and other stakeholders to bring innovative medical solutions to market. Enhance Patient Safety: Apply your expertise in software/firmware, network functionality, and cybersecurity to protect patient data and device functionality. Mitigate Risks: Participate in risk management, design verification/validation, and complaint evaluation to ensure our products are safe and reliable. Ensure Excellence: Maintain compliance with quality system standards and ensure documentation accuracy, contributing to the overall quality and success of our products.

What We Need:

B.S. in Computer Science, Software Engineering, Biomedical Engineering, Life Science, or related field (MS preferred). 5+ years of experience in design control processes – as a developer or quality professional Familiarity with tools like HP Quality Center, Siemens Teamcenter, and IBM DOORS. Knowledge of FDA regulations, ISO guidelines, and IEC 62304 standards.

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