Medical Device Engineer / Scientist - Design Verification | Device Engineer / Scientist (m/w/d) – Design Verification & Medical Devices

expertum GmbH

Ingelheim am Rhein, Rheinland-Pfalz, Deutschland
Published Feb 24, 2026
Full-time
No information

Job Summary

This role involves the end-to-end design verification and development of innovative medical and combination products within the pharmaceutical industry. As a Device Engineer, you will be responsible for planning, executing, and coordinating design verification studies, while ensuring all activities comply with strict regulatory standards such as the Medical Device Regulation (MDR) and FDA requirements. You will act as an Evaluation Engineer within interdisciplinary teams, collaborating closely with experts in Design Engineering, Quality Development, Risk Management, and Usability Engineering. The position offers a unique opportunity to contribute to successful product approvals in a highly regulated environment. It is particularly attractive for its hybrid working model (2-3 days remote), indefinite contract, and a competitive salary aligned with the chemical industry's collective agreement. This is an ideal role for a professional looking to work on cutting-edge medical technologies at a renowned pharmaceutical location in Ingelheim am Rhein.

Required Skills

Education

University 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 devices or combination products
  • Proven experience in the planning, execution, and documentation of design verifications
  • Extensive experience with Design Control processes according to international standards
  • Professional experience working within interdisciplinary development teams

Languages

Not specified

Additional

  • Location: Ingelheim am Rhein; Hybrid work model (2-3 days home office per week); Indefinite contract; Compliance with MDR and FDA regulations required.