About AbbVie AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job title: Manager Clinical Supply Labels Main: Responsible for the planning, implementation, monitoring and documentation of the design and printing of labels for clinical trial samples of pharmaceuticals and medical devices used worldwide in compliance with legal requirements, in particular GMP guidelines Annex 13, EU Clinical Trial Regulation (EU CTR) and Medical Devices Regulation (EU MDR). Professional and disciplinary management of the employees as well as responsibility for the training of the subordinate employees Information, promotion and further training of subordinate employees and assessment of performance and cooperation behaviour. Independent content and scheduling planning and coordination of processes with the units Bulk Goods Manufacturing, Analytics, Clinical Supply Pharmacy, Clinical Supply Materials Management, Quality Assurance, Clinical Operations and Regulatory Affairs in Ludwigshafen, Lake County and other AbbVie locations worldwide. Review and approval of documentation as part of label design, label printing and GMP-compliant label testing. Responsible for the further development of concepts and for the further development of the globally used software for the provision of clinical investigational medicinal products Leading cross-functional teams to harmonize operations at local and global levels, as well as with external clinical label manufacturers. Investment planning and realization in terms of premises and equipment for the Clinical Supply Labels sector. Ensuring a functional and targeted infrastructure Preparation of work instructions (SOPs) for GMP matters in the context of label preparation and in the context of the packaging of clinical trial samples. Qualifications Request: Successfully completed pharmacy studies and license to become a pharmacist Several years of professional experience in personnel management Professional experience in the design and manufacture of labels for clinical trial samples of pharmaceuticals and medical devices Fluent in spoken and written English Reisebereitschaft 5% Duration: Unlimited Travel Yes, 5 % of the Time Job Type Experienced Schedule Full-time Job Level Code IC Equal Employment Opportunity 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.