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# Systems Engineer

- **Company:** AbbVie Deutschland GmbH & Co. KG
- **Location:** Ludwigshafen am Rhein, Germany
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Systems Engineering, Configuration Management, Failure Mode Effects Analysis, Software Requirements Analysis, Systems Architecture
- **Published:** August 14, 2026
- **Apply:** https://dejobs.org/x/x/36FEAA27248A4C3198E8B232C601D637/job/

## About the Role

third-party development activities and ensure alignment of Design Control and Quality by Design activities. + Collaborate with cross-functional team members to identify process gaps, recommend and implement improvements, and help standardize methods and ways of working to enhance consistency, efficiency, operational effectiveness, and the development of sustainable business and organizational strategies. + Collaborate with cross-functional teams to plan and coordinate testing activities, including sample and laboratory resource planning, and drive improvements to processes, methods, and ways of working. + Serve as the dedicated systems engineer for projects, independently owning key deliverables and coordinating stakeholder input as needed to support successful execution. Qualifications This is how you make a difference: + Bachelor's degree in Engineering, Science, or a closely related discipline with 7+ years of relevant experience, or a Master's degree with
5+ years of relevant experience. + Proven ability to provide technical leadership, ensuring system design and documentation comply with applicable safety and regulatory requirements. + Expertise in product development from initial concept to release to market is desired with direct experience in combination product or medical device development and familiarity with FDA 21 CFR Part 820.30, 21 CFR Part 4, ISO14971, ISO 13485 and EU MDR preferred. + Strong Expertise in Systems Engineering principles including user and stakeholder need definition; requirements definition; risk management, product architecture, configuration management, traceability, and change management + Expertise in DHF management and creating various Design Control documents in compliance with regulations. + Strong analytical and problem-solving skills, with the ability to resolve key project challenges, make sound decisions, identify risks, and develop appropriate mitigation plans. + Experience

## Description

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! Together, we break through - as Senior Systems Engineer (all genders) We are looking for a Senior Systems Engineer to join our Device and Combination Product Development team in R&D. You will contribute to the development of exciting new aesthetic devices and therapeutic combination products for various phases of clinical studies and work closely with cross-functional colleagues in operations as programs transition to commercial development. In this role you're also responsible for integration of inputs and risks from multiple disciplines to ensure robust patient-centric product design and performance. In this role, you
will be working with a global team of exceptional scientists, engineers, and leaders on a variety of devices, drug delivery systems from syringes to autoinjectors to complex electromechanical pumps, with a focus on Aesthetic Filler devices. Your expertise and leadership will ensure these systems are safe and effective in meeting their intended use for clinical and commercial development programs. Make your mark + Drive the implementation of holistic Systems Engineering principles within the Design Controls process, with a focus on system architecture and integration, Design Inputs, traceability, risk management, change management, and DHF architecture. + Define and manage user and stakeholder needs, use cases, product requirements, and applicable standards throughout the product development lifecycle. + Lead system and use-related risk management activities, including risk planning and reporting, system risk assessments, and design and process FMEAs. + Oversee and integrate


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