Quality Assurance Documentation Specialist m/w/d

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Your AbbVie Talent:

Associate Degree in Secretarial Sciences, Business Administration or Natural Sciences
Minimum of five (5) years of experience in the pharmaceutical industry.
Minimum of five (5) years of experience in administrative documentation management.
Very good knowledge of IT documentations systems e.g. Attaché, Attaché Pro, QMD, EDOS, dSIG
Very good understanding of the processes of an operations site (manufacturing, packaging, QC, QA) and GMP
Very good English skills
Excellent knowledge of regulatory requirements for GMP documentation system and personnel training
We Offer
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A fantastic opportunity to work in in a world-class team.
A supportive environment that allows you to focus on your role and tailor your work to your individual needs, including flexible work models, multiple benefits, and comprehensive health and sports programs.

Attractive compensation and company benefits, including our excellent occupational health management system, which is one of the best in Germany.
Your Application
We are looking forward to your online application.
An equal opportunity employer. AbbVie welcomes and encourages diversity in our workforce.
Learn more about AbbVie Deutschland at
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for more information about the therapeutic areas in which we’re active.
Additional Information

Equal Employment Opportunity Employer

At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

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