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Abbott (Senior) Specialist Regulatory Affairs (m/f/d) in Hamburg, Germany

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 107,000 colleagues serve people in more than 160 countries.

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In Germany, Abbott has more than 3,000 employees working in manufacturing, research and development, logistics, sales and marketing. They are located at Abbott`s German headquarters in Wiesbaden and its sites in Hanover, Neustadt am Rübenberge, Wetzlar, Eschborn, Witten, Cologne and Jena. Abbott Automation Solutions in Hamburg (formerly GLP Systems) is now Abbott.

The Abbott Automation Solutions GmbH in Hamburg is the international specialist for laboratory automation. The modular automation solution includes a single sample transport, which allows the dynamic connection of analytical instruments as well as platforms for sample preparation and archiving in laboratories of almost all sizes. This innovative solution is characterized by high efficiency in sample throughput, by flexibility in the design of the laboratories and thus by cost advantages for our international customers.

Abbott Automation Solutions is looking for a

(Senior) Specialist Regulatory Affairs (m/f/d)

based in Hamburg.


  • Support all regulatory activities related to the site in Hamburg

  • Conduct regulatory assessment of design changes, define regulatory strategies and prepare notifications for worldwide submissions

  • Assist in creation and maintenance of submission documents

  • Compile and submit documentation for product certifications and re-certifications

  • Support product registrations and procurement of legal documents

  • Build interfaces to regulatory agencies, provide submissions and assist in audits

  • Collaborate with site operations and production partners to assure compliance of manufactured products to international regulations, act as regulatory representative in cross-functional teams

  • Establish and maintain relationships to Abbott sites and production partners


  • Technical degree in natural sciences, medical engineering or equivalent

  • Profound experience in Regulatory Affairs

  • Background in IVD or medical devices industry (preferably in regulatory, quality, manufacturing, R&D or related functions)

  • Excellent German and English language skills (verbal and written)

  • Good organizational skills

  • Good interpersonal and communication skills

The positions will be limited for two years.

Abbott Germany has a range and variety of jobs on offer in a positive and dynamic environment that allows you to maintain a healthy work-life balance. We provide development opportunities as part of our comprehensive Talent Management Program. Your contribution to the company’s success will be rewarded with a competitive salary package. We offer comprehensive benefits to suit the lifestyles of all our employees, from a retirement plan that is far above market average, a save-as-you-earn program, to educational scholarships for children, and health management initiatives for staff and their dependents.

Do you like the sound of this job and think you’ve got what it takes? Then send us your CV today. We look forward to receiving your application.

Discover at why candidates choose a career with Abbott in Germany.

AN EQUAL OPPORTUNITY EMPLOYER - Abbott welcomes and encourages diversity in our workforce.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email