Engineer, Automation (all genders) | 2-Year Contract | Full-Time

About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

A role where your passion can make a difference? We offer it. A promising outlook for your future? We offer that, too! Welcome to AbbVie! As part of an international company with approximately 48,000 employees worldwide and around 3,000 employees in Germany, you will play an active role in addressing tomorrow’s healthcare challenges with us. Are you passionate about advancing healthcare worldwide and using your expertise to improve patients’ quality of life? Would you like to do so in a challenging work environment that enables you to further develop your skills? Then AbbVie is the right place for you! As a team member in our Manufacturing & Engineering (M&E) department, you will be responsible for the automation systems used in pharmaceutical production and packaging facilities. Put your expertise to work and join our team at the Ludwigshafen site as an Automation Engineer (all genders). Here, you will make a real impact. Specifically, you will: Ensure the availability of the various automation systems across the different production areas. In the event of a malfunction, you will act as the technical expert and, in close cooperation with other departments and the manufacturer, take all necessary measures to resolve the issue promptly and in compliance with GMP requirements. Implement automation projects for pharmaceutical production facilities in a regulated environment throughout the entire system life cycle. You will work closely with business partners, external service providers, and suppliers, coordinate all stakeholders, and take on selected project management responsibilities. Act as a subject-matter representative, working closely with Production, Maintenance, Equipment Engineering, Qualification, and Quality Assurance. You will also be a member of international project teams. Develop proposals for long-term adaptations and the continuous improvement of control systems. As part of capital investment projects, develop the design and requirements specifications for the automation of production facilities. Ensure compliance with regulatory requirements relating to data integrity and data security, both for existing systems and new implementations. Prepare, review, and approve the required technical and project-related documentation. You will also verify compliance with applicable standards, guidelines, and internal requirements. In addition to ensuring contractual performance, you will ensure compliance with GMP requirements. Participate in inspections conducted by internal and external organizations within your area of responsibility.

Successfully completed a degree in engineering, such as Automation Engineering, Electrical Engineering, or Mechatronics. Initial professional experience in electrical engineering, automation, or a related field. Experience with PLC programming and visualization systems. Excellent knowledge of Microsoft Office and Microsoft client and server operating systems. Knowledge of machine vision systems, such as Cognex, is desirable. Experience designing and implementing automation projects is preferred. Initial experience working in a GMP- and pharmaceutical environment is desirable. Innovative, analytical, systematic, and results-oriented approach to work. Hands-on mentality, strong initiative, and perseverance. Practical,