Dornier MedTech is a medical device company headquartered near Munich, Germany, and a wholly owned subsidiary of Advanced MedTech. As a pioneer in the field of urology, Dornier is one of the most trusted names in the industry.

With the introduction of several breakthrough technologies and revolutionary therapies in recent years, we continue to drive medical performance and pioneer innovation in urology. As the world's first MDR-certified integrated urology company and one of the founders of the Urology Care Foundation (formerly known as the American Foundation for Urologic Diseases), we pride ourselves on holding ourselves to the highest standards of patient safety and product efficacy.

Today, we are setting new standards in digital urology to provide holistic care to patients seeking treatment and support the community on their road to recovery, both online and on-site.

Trusted by thousands of physicians and patients, Dornier is committed to supporting our urological communities worldwide.

Development, implementation, construction and testing of electrical components and for medical products, which represent state-of-the-art technology. The job holder closely collaborates with stakeholders across department and operational structures, particularly with engineers from other groups such as systems engineering, quality engineering, software development but also regulatory affairs and quality management.
Focus is on delivering innovative solutions that meet customer requirements as well as regulatory requirements, particularly those related to safety and effectiveness. The deliverables contribute to increasing the competitiveness and commercial success of Dornier MedTech and its subsidiaries. Solutions are provided in a cost- and time-efficient manner and by strong collaboration with stakeholders across department and operational structures.

Specific Responsibilities

Development and implementation of power and control electronic boards for complex medical devices.
Creation of electrical circuit and wiring diagrams for complex medical devices.
Development and implementation of electrical safety concepts to assure product functional safety.
Implementation and execution of concepts for product cost reduction.
Collection and determination of technical requirements and specifications.
Create component and system specifications and other quality related documents such as risk analysis, DFMEA, test and verification reports, etc. in compliance with international requirements (CE, FDA, MHLW).
Perform verification tests to verify electrical components and product requirements.
Maintain products and systems to ensure stable and reliable operations as part of the product lifecycle management process.
Support of troubleshooting electrical-related issues in production
Performing of engineering tasks during setup and start-up of prototypes
As needed, coordinate, organize, and track engineering tasks on a task- or project-specific basis
Assisting the project management with the planning of engineering-related tasks
Representation of the Engineering department in project team meetings
Coordinate and work with third-party suppliers and contractors
Monitoring of technological trends in electronics, including reviews of competitors' technology.

Masters's degree in science and engineering with experience in R&D
Specialization in electrical engineering
At least 7 years of experience in the development of electrical devices, preferably medical systems
Advanced knowledge of electronics (power-, digital-, analog- and microprocessor technology)
Experienced in design and development of power and digital electronic boards
In-depth knowledge of EMI/EMC design principles and electrical safety requirements
Experience in creating electrical schematics and circuit diagrams
Experience working with PC-controlled systems
Experienced in creating technical reference documentation
Knowledge in requirements and systems engineering
Experienced in performing Design Transfer to production
Creativity and analytical skills
Assertiveness
Demonstrated ability to work and contribute in a team environment
Strong work ethic with pride in individual accomplishments
Interested in personal and professional growth for her-/himself and team
Entrepreneurial spirit very helpful in a small but global organization
Motivated and creative, ability to “think outside the box”
Be able to function independently of direct supervision
Standards knowledge: ISO 13485, FDA 21 CFR 820.30, IEC 14971, IEC 62366, IEC 60601-1, IEC 60601-1-2 and collateral standards
Ms Office; Outlook, Word, Excel, PowerPoint
Knowledge in ERP system; Preferably Infor SyteLine
Knowledge in Altium, Eagle, OrCAD PSpice, Multiphysics simulation, MATLAB
Knowledge in requirement management tool such as DOORS, Polarion or CodeBeamer
Knowledge in building PCB prototypes and system cabling

Personal induction plan and comprehensive onboarding
Flexible working hours
30 days of holiday
interesting tasks in a dynamic, international environment
Continuous training and development
Flat hierarchies
Attractive canteen
Free coffee, tea and water
Employee events
Charging stations for electric cars
Accident insurance
Employer contribution to VWL
Employee fund with various allowances and subsidies
Free language courses

KA1SP_DE

✨ قدّم بالذكاء الاصطناعي – يتولى خطاب التقديم والإرسال

تفضّل القيام بذلك بنفسك؟ التقديم مباشرةً لدى الجهة المعلِنة · المصدر: Stepstone

الوظائف حسب المصدر

كل المصادر Jobware 4,362 StepStone 63,181