Device Engineer / Scientist – Design Verification & Medical Devices | Device Engineer / Scientist (m/w/d) Design Verification & Medical Devices
expertum GmbH
Job Summary
This role is centered on the design verification and development of medical and combination products within the pharmaceutical industry. As a Device Engineer, you will be responsible for planning, executing, and coordinating design verification studies, including the creation of verification plans and regulatory reports. You will act as an Evaluation Engineer within interdisciplinary teams, collaborating closely with Design Engineering, Quality Development, and Risk Management to ensure product excellence. A key part of your day-to-day will involve navigating complex regulatory landscapes, ensuring compliance with MDR and FDA standards to support successful product approvals. This position is particularly attractive due to its hybrid work model (2-3 days remote), participation in innovative product development, and a salary structure aligned with the chemical industry's collective bargaining agreements. It offers a long-term career path with an indefinite contract and opportunities for funded professional development.
Required Skills
Education
Completed degree in a Life Sciences discipline (e.g., Medical Technology, Biotechnology, Pharmacy, Engineering, or Natural Sciences).
Experience
- Several years of professional experience in the regulated development environment of medical or combination products
- Proven experience in the planning, implementation, and documentation of design verifications
- Professional experience working within Design Control processes (e.g., 21 CFR 820.30 or MDR)
- Experience in interdisciplinary team coordination and interface management
Languages
Additional
- Hybrid work model (2-3 days home office per week). Location: Ingelheim am Rhein. Indefinite employment contract.
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