Product Configuration Management Specialist (w/m/d)

We are one of the world's leading companies in orthopaedics, arthroscopy, sports medicine and orthobiology. True to our Mission Helping Surgeons Treat Their Patients Better, we have been developing innovative products and surgical procedures for 40 years. Arthrex was founded in Munich in 1981 - today our headquarters in Naples (Florida, USA) with further branches in 29 countries. Our corporate culture is characterised by cross-border cooperation and an exchange with colleagues from different nationalities. The development of new business areas and the expansion of our product range contribute to a steady growth and will lead us to the development of high-quality products in the future. Our employees contribute significantly to this success with their commitment. For this we offer a motivating, value-adding working environment.

As a Product Configuration Management Specialist, you create and maintain important objects associated with product lifecycle management in global systems, ensuring compliance with product release schedules, data integrity and compliance You check and implement change requirements in product lifecycle management to create or update product attributes, structures and related objects according to the requirements of different departments In addition, you will take care of the transfer and integration of data between PLM and ERP systems and will be responsible for ensuring and documenting quality management rules and standards You take over the internal guidance and support of the specialist departments in the application of the global ERP system in terms of PLM data as well as in process, document and data-related activities You are also responsible for the proactive identification and implementation of improvement potentials for daily workflows They are in close contact with global teams from product management, design technology, supply chain, quality assurance, regulatory affairs, operation, finance and master data management to ensure successful cooperation

They have a university degree with a focus on IT as well as experience in medical technology or pharmaceutical industry In addition, you will bring multi-year experience with SAP master data and data management (including technical change management) You have a very good understanding of ISO standards (13485, 90001), FDA and EMA regulations and other relevant requirements related to the control of documents and records You can successfully apply your multi-year experience in Agile or other PLM, Documentum, SAP or other relevant software applications Your organizational talent and your structured, conscientious and reliable operation combined with a strong interest in details, procedures and processes, as well as the ability to work in a fast-paced environment With the current MS Office programs you are well familiar, fluent knowledge of the German and English language complete your profile

An activity in an international environment Personal and esteeming coexistence A future-proof workplace Individual incorporation, supplemented by extensive introduction training Occupational pensions (indefinite employment) Free additional hospital insurance Support in various situations of life (e.g. childcare, care, personal questions, etc.) through cooperation with a service provider From Monday to Thursday free lunch