Stellenbeschreibung The job that makes possibilities real in patients' lives. And yours. The job that helps you get ahead in life. Moving mountains together. Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place! Moving mountains together – as Senior Scientist I, Engineering – Method Development (all genders) (full-time, permanent) We are looking for an experienced Senior Scientist I, Engineering – Method Development (all genders) to join our Device and Combination Product Development to contribute to the development of exciting new drug / device combination products. Your tasks and responsibilities Subject Matter Expert (SME) for Test Method Development of delivery devices and combination products: Test Method development, including best practices for universal implementation, Test Method Validation/Transfer. Design Verification: Author verification protocols and reports. Support investigations and issue resolutions. Execute test protocols supporting exploratory and verification testing, analyze data, document in lab notebooks, and present results to cross-functional teams. Utilize Zwick Universal Test Machine (UTM) and other GMP and non-GMP test equipment used for combination product development and Design Verification. Software Tools: Utilize Electronic Lab Notebook (ELN) software and electronic DHF tools such as Polarian. Implementing process automation and digitalization initiatives to enhance efficiency and reliability in device development and manufacturing processes. Utilizing analytical modelling for key performance attributes and ensuring compliance with regulatory requirements, including FDA, EMA, and ISO standards.