Risk Management Engineer (m/w/d) Medical Devices
Join to apply for the Risk Management Engineer (m/w/d) Medical Devices role at TECCON Consulting GmbH
Risk Management Engineer (m/w/d) Medical Devices
2 days ago Be among the first 25 applicants
Join to apply for the Risk Management Engineer (m/w/d) Medical Devices role at TECCON Consulting GmbH
Are you an expert in your field and ready to apply your know-how to exciting projects?
As part of the Hamburg-based TECCON Group—with over 450 employees in IT, engineering, and business—we develop innovative solutions for renowned clients. Our mission is to recognize and nurture human potential by creating tailored connections between companies and talent. Contribute your expertise to our projects and help shape the future.
* Risk Management Documentation: Consolidate input from cross-functional teams to compile risk management documentation for the Design History File (DHF) and Device Master Record (DMR) in compliance with ISO 14971.
* Design Verification & Control Strategy: Define and support design verification and process control activities; identify and communicate device-related risks and project challenges to stakeholders.
* Scientific Writing for Regulatory Submissions: Prepare high-quality scientific documentation for external partners and health authorities; contribute to regulatory submission packages.
* Cross-Functional Collaboration: Provide scientific and technical guidance within interdisciplinary teams and actively promote internal knowledge exchange.
* Project Planning & Timelines: Develop and manage detailed development plans and timelines in alignment with project leads and the cross-functional team.
* Educational Background: Master’s degree in Engineering or a related field (e.g., Medical Engineering, Mechanical Engineering, Process Engineering, Electrical Engineering, Computer Science) or equivalent practical experience.
* Language Skills: Strong command of English (spoken and written); knowledge of German is an asset.
* Industry Experience: Previous experience in medical device development or the pharmaceutical sector is advantageous.
* Risk Management Expertise: Familiarity with FMEA, ISO 14971, or similar standards in the field of risk analysis.
* Application Knowledge: Experience with Polarion or comparable requirements and risk management tools beneficial.
* Exciting challenges and responsible tasks with plenty of creative freedom and personal responsibility
* Long-term career prospects in a dynamic and dedicated team
* Flexible working hours and remote work options to support a healthy work-life balance
* Diverse development and training opportunities to help you reach your full potential
* Engaging team events that strengthen team spirit and add variety to your work life
The gross annual fulltime salary is at least EUR 60.000 € but of course we offer overpayment in line with the market, depending on qualifications and professional experience.
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Full-time
Job function
* Job function
Research, Science, and Engineering
* Industries
Pharmaceutical Manufacturing
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