Senior Engineering Consultant Firmware / Software / Hardware / Projektmanagement in der Medizintechnik
Aktualisiert am 08.07.2026
Profil
Freiberufler / Selbstständiger
Remote-Arbeit
Verfügbar ab: 08.07.2026
Verfügbar zu: 100%
davon vor Ort: 100%
Embedded Systems
Projektmanagement/Projektleitung
Embedded Software
DIN 13485
IEC 60601
IEC 62304
ISO 14971
FDA
Medizinprodukte
Healthcare
Schaltplan
Layout
Softwarearchitektur
Requirements Engineering
Testautomatisierung
Lifecycle Management
ALM
Versionsverwaltung
Azure Devops
Firmware
Hardware-Design
German
native
English
fluent in speech and writing
French
basic knowledge

Einsatzorte

Einsatzorte

Weßling, Oberbayern (+100km)
Deutschland, Schweiz, Österreich
möglich

Projekte

Projekte

2 Jahre 6 Monate
2024-01 - 2026-06

novel, fully implantable pacemaker

Requirements management, Firmware development, Design documentation, Testing, Support project management Embedded C Azure Devops Testautomatisierung ...
Requirements management, Firmware development, Design documentation, Testing, Support project management
Firmware development for a novel fully implantable pacemaker (Class III, active implant)
  • Definition of product and software requirements
  • Definition of software architecture
  • Design documentation
  • Implementation of firmware according to IEC62304 (C)
  • Creation of automated test and build environment
  • Creation and performing of unit, functional and integration tests
  • Support in electronics development
  • Support in project management
  • Support in FDA audits
Embedded C Azure Devops Testautomatisierung Testautomatisierungstools CodeCoverage Code-Analyse Requirements Management Requirements Engineering Risikomanagement IEC 62304 DIN 13485 ISO 14971 IEC 60601 Softwarearchitektur
Cairdac
Paris (France)
7 Jahre 5 Monate
2019-02 - 2026-06

Product development for a fully implantable pump

Requirements management, Firmware development, Hardware/electronics development, Design documentation, Testing, Support project management Aktives Implantat
Requirements management, Firmware development, Hardware/electronics development, Design documentation, Testing, Support project management
Product development for a fully implantable pump to cure fluid overload, including inductive charger and programmer tablet (Class III, active implant)
  • FDA Submission of existing product
    • Update of requirements and creation of design documentation
    • Creation of cyber security risk assessment, update of design FMEA
    • Creation of unit tests, performing Firmware / Hardware verification
  • Next generation implantable pump
    • Requirements management
    • Update of electronics for implantable pump and inductive charger (Altium Designer)
    • New firmware for implantable pump and inductive charger (C, RTOS)
    • Design documentation
    • Creation of unit, functional, integration, and acceptance tests
    • Version and configuration management
  • Secure upload and storage of data in cloud
    • Requirements management
    • Implementation of secure (HTTPS, MQTTS) upload of data from external charger
    • ?Supplier selection of cloud service provider
  • Support in project management
  • Support in FDA audits
Aktives Implantat
Sequana Medical NV
Zurich (Switzerland)
4 Jahre 1 Monat
2019-07 - 2023-07

Product development of implantable and external components

Project management, Requirements management, Firmware development, Hardware development, Risk management, Design Documentation, Testing IEC 60601 DIN 13485 IEC 62304 ...
Project management, Requirements management, Firmware development, Hardware development, Risk management, Design Documentation, Testing
Product development of implanted and external components for an fully implantable heart support device (Class III, active implant)
  • Responsible for all activities for the product development of all external, patient-worn components
  • Responsible for all power and communication related components of the implant
  • Responsible for system to upload data from implant to a central data server
  • Development of firmware for above mentioned components (C, RTOS)
  • Development of application and server software using (C#/.Net)
  • Development of electronics for above mentioned components (Altium Designer, Spice)
  • Support for development of mechanics (SolidWorks)
IEC 60601 DIN 13485 IEC 62304 Requirements Requirements Management ALM Lifecycle Management Softwarearchitektur Schaltplan Layout Aktives Implantat
Syntach AB
Lund (Sweden)
1 Jahr 8 Monate
2021-10 - 2023-05

Test systems ? extracorporeal heart pump

Software development, documentation, testing
Software development, documentation, testing
Development of a test system for an extracorporal heart pump
  • Development of firmware for ARM (C)
  • Development of application test software (C#/.Net)
  • Creation of the integration and acceptance tests
  • Design documentation
Livanova
Pittsburgh (USA)
1 Jahr 2 Monate
2021-07 - 2022-08

wireless power transfer for an active neuro- or cranial implant

Electronics development, Coordination of suppliers, Prototype testing
Electronics development, Coordination of suppliers, Prototype testing
Development of a wireless energy transmission system for an active neuro/ cranial implant.
  • Development of power sender and receiver electronics (Altium Designer)
  • Selection and Management of suppliers
  • Creation of verification tests
  • Design documentation
Longeviti Neuro Solutions
Baltimore (USA)
3 Jahre 1 Monat
2017-04 - 2020-04

Electronics and firmware for automotive torque measuring instruments

Software development, Electronics development, documentation, testing
Software development, Electronics development, documentation, testing
Development of electronics and firmware for torque measurement devices located in cars
  • Development of 
    • firmware (C, Atmel Studio)
    • application test software (C#/.Net)
    • ?electronics (Altium Designer)
  • Definition and implementation of unit, integration and acceptance tests
Axon System GmbH
Inning (Germany)
8 Jahre 2 Monate
2010-12 - 2019-01

Establishing and managing the development department

Chief Technical Officer (CTO) since March 2012, previously Head of Development in Software & Electrical Engineering
Chief Technical Officer (CTO) since March 2012, previously Head of Development in Software & Electrical Engineering
Development and management of the development department, Monitoring of all development activities and project management, Technical Company representative towards customers, investors and suppliers
  • Coordination of all development projects
  • Allocation of resources and budgets in collaboration with the project leaders
  • Assist project leaders in planning development tasks
  • Definition of staff goals, tracking the defined goals, staff training
  • Definition of internal development and quality standards in software-, electrical- and mechanical engineering
  • Planning and managing projects (> 5 million budget, > 15 employees)
  • Hands-on focus on software development and electrical engineering
  • Internal audits and external audits
  • Support in risk management
DUALIS MedTech GmbH
Seefeld (Germany)
3 Jahre 8 Monate
2014-07 - 2018-02

Development, production and distribution of the NeoCare baby monitor

Chief Executive Officer (CEO), Founder, Shareholder
Chief Executive Officer (CEO), Founder, Shareholder
Development, production and sales of NeoCare baby monitor, the next generation baby monitor including vital sign tracking.
  • Building up company from scratch
  • Oversee all software development activities.
  • Software and algorithm development
  • Big data and cloud storage
  • Responsible for all sales and investor related activities
on request
Wessling (Germany)
3 Jahre 3 Monate
2007-12 - 2011-02

Further development of comprehensive network and file management software

Consultant in software development
Consultant in software development
Further development of a comprehensive network and file management software for the mainframe BS 2000 and Unix derivatives. Further development of a comprehensive text, hex and binary editor for Dos, Windows and Unix
  • Conception and development of APIs.
  • Development of test environments
  • Implementation of customer requirements
OPG ? Online Programmierung GmbH
Munich (Germany)
3 Jahre 3 Monate
2007-10 - 2010-12

Project management, Quality Management consulting, Regulatory affairs, Software development, IT consulting

Project management, company strategy consulting, implementation, and monitoring of a quality management system according to EN ISO 13485: 2003/ AC: 2009, development of approval strategies for active implants, software development, support of the IT infrastructure
  • Definition of project goals from the requirements
  • Project planning and structuring
  • Risk assessments, cost planning, resource planning
  • Project implementation and follow-up, technical guidance of assigned employees
  • Project Reviews
  • Planning, design and partial implementation of an infrastructure for storing patient data in cloud storage, big data
  • Planning, design and development of a web-based frontend to view patient data (GWT and Java) and Windows clients (C ++ / C #)
  • Planning, conception and partial development of software for embedded systems (ARM, Windows / Linux, ASM / C / C ++), control of data buses (CAN / SPI / SSP / I2C / UART, USB) for the connection of peripherals (Bluetooth, MICS , Displays, buttons, ...)
  • Development, implementation and monitoring of quality management systems and training in accordance with EN ISO 13485
  • Implementation of risk management
  • Supervision of external audits and internal audits
  • Regulatory affairs, cooperation with notified bodies
DUALIS MedTech GmbH
Seefeld (Germany)
4 Jahre 5 Monate
2004-08 - 2008-12

Development of complex computer games and other consumer entertainment products for PC and console

Chief Executive Officer (CEO), Chief Technical Officer (CTO), Founder, Shareholder Windows ASM / C / C ++ / C # openGL / DirectX
Chief Executive Officer (CEO), Chief Technical Officer (CTO), Founder, Shareholder
  • Lead game engine programmer
  • Development of a computer game based on a specially developed 3D engine and middleware
  • Negotiations with publishers and other investors
  • Public relation
  • Budget controlling, reporting, project management
Windows ASM / C / C ++ / C # openGL / DirectX
on request
Wuppertal (Germany)
1 Jahr 1 Monat
2006-10 - 2007-10

Project management, development of software for different mechatronic systems

Conception and development of hardware-related software.
  • Control of various displays, input devices and radio modules for a control and monitoring handheld for an artificial sphincter implant (ARM7, ASM / C).
  • Development of monitoring and evaluation software for in vivo tests
  • Design and EMC simulation of an antenna for implants (402-406 MHz).
  • Development of a motor controller for brushless motors.
  • Control based on various sensors and physiological values.
  • Design of evaluation boards.
German Aerospace Center (DLR)
Oberpfaffenhofen (Germany)

Aus- und Weiterbildung

Aus- und Weiterbildung

4 Jahre 9 Monate
2001-10 - 2006-06

Study of Computer Science

Diploma, Technical University of Munich
Diploma
Technical University of Munich
Main focus technical computer science and electrical engineering

Position

Position

  • Senior Medical Device Consultant in R&D, Regulatory and Team Management
  • Senior Engineering Consultant im Bereich Firmware, Hardware und Software Entwicklung, mit Schwerpunkt Medizintechnik

Kompetenzen

Kompetenzen

Top-Skills

Embedded Systems Projektmanagement/Projektleitung Embedded Software DIN 13485 IEC 60601 IEC 62304 ISO 14971 FDA Medizinprodukte Healthcare Schaltplan Layout Softwarearchitektur Requirements Engineering Testautomatisierung Lifecycle Management ALM Versionsverwaltung Azure Devops Firmware Hardware-Design

Schwerpunkte

  • Firmware/ Software development for medical devices
    • Conception and Definition of software requirements
    • Architectural design, design documentation, software risk management
    • Implementation
    • Unit testing, verification and integration testing
  • Electrical Engineering for medical devices
    • Conception and Definition of hardware requirements
    • Schematics and Layout, Hardware design documentation and FMEA
    • Verification and Integration testing
    • Transition to manufacturing
  • Project Management
    • Definition of project goals, planning and control
    • Development and introduction of project management processes
    • Release, change and configuration management
  • Team leadership
    • Building and disciplinary leadership of teams
    • Communication, motivation, and conflict resolution
    • Mentoring with hands-on mentality
  • Quality management
    • Development of new and optimization of existing quality processes
    • Carrying out internal audits and supporting external audits
  • Regulatory Affairs
    • ?Support for creation of design dossier for submissions

Produkte / Standards / Erfahrungen / Methoden

Skills
  • ALM & PM Tools
    • Jira, Perforce Helix ALM, Trac, MS Project
  • Versoning & CI Tools
    • Azure Devops, GIT, Jenkins, Subversion
  • Standards (extract)
    • Medical device software ? Software life cycle processes (IEC 62304)
    • Medical devices - Quality management systems (ISO 13485)
    • Medical devices - Application of risk management to medical devices (ISO 14971)
    • Medical electrical equipment (IEC 60601),
    • Medical devices - Application of usability engineering (IEC 62366)
  • Operating Systems and SDKs
    • Windows, Linux, WSL, ThreadX, TI RTOS, FreeRTOS, Keil RTOS, QF Framework, Azure and AWS
  • Hardware Systems
    • ARM / Cortex Controllers, MSP430, AVR, 8051, Intel X86/X64, iPhone, Android
  • Bus Systems
    • Ethernet, CAN, CANFD, SPI, SSP, I2C, UART, 1-Wire, USB, USB-PD, ?
  • Wireless Systems
    • WLAN, Bluetooth, 433/868 MHz, MICS, MedRadio, ZigBee, NFC
  • Software IDEs
    • VS Code, Eclipse IDEs, Keil uVision, Visual Studio, IAR Workbench, AVR Suite, Labview,
  • Hardware EDA
    • Altium Designer, Eagle, Spice
  • Mechanical Tools
    • Solidworks

Professional experience

2001 - today
Firmware/ Software development

2006 - today
Electrical Engineering

2007 - today
Project management and Quality and Regulatory Affairs

2010 - today
R&D Management since 2010

Programmiersprachen

  • C
  • C++
  • C#
  • Objective-C
  • Java
  • Assembler
  • LabVIEW
  • Python
  • HTML
  • CSS
  • Javascript

Branchen

Branchen

Umfangreiche Erfahrung im regulativen Umfeld der Medizintechnik. Betreuung der Kunden bei internen und externen Audits durch FDA & benannte Stelle

Einsatzorte

Einsatzorte

Weßling, Oberbayern (+100km)
Deutschland, Schweiz, Österreich
möglich

Projekte

Projekte

2 Jahre 6 Monate
2024-01 - 2026-06

novel, fully implantable pacemaker

Requirements management, Firmware development, Design documentation, Testing, Support project management Embedded C Azure Devops Testautomatisierung ...
Requirements management, Firmware development, Design documentation, Testing, Support project management
Firmware development for a novel fully implantable pacemaker (Class III, active implant)
  • Definition of product and software requirements
  • Definition of software architecture
  • Design documentation
  • Implementation of firmware according to IEC62304 (C)
  • Creation of automated test and build environment
  • Creation and performing of unit, functional and integration tests
  • Support in electronics development
  • Support in project management
  • Support in FDA audits
Embedded C Azure Devops Testautomatisierung Testautomatisierungstools CodeCoverage Code-Analyse Requirements Management Requirements Engineering Risikomanagement IEC 62304 DIN 13485 ISO 14971 IEC 60601 Softwarearchitektur
Cairdac
Paris (France)
7 Jahre 5 Monate
2019-02 - 2026-06

Product development for a fully implantable pump

Requirements management, Firmware development, Hardware/electronics development, Design documentation, Testing, Support project management Aktives Implantat
Requirements management, Firmware development, Hardware/electronics development, Design documentation, Testing, Support project management
Product development for a fully implantable pump to cure fluid overload, including inductive charger and programmer tablet (Class III, active implant)
  • FDA Submission of existing product
    • Update of requirements and creation of design documentation
    • Creation of cyber security risk assessment, update of design FMEA
    • Creation of unit tests, performing Firmware / Hardware verification
  • Next generation implantable pump
    • Requirements management
    • Update of electronics for implantable pump and inductive charger (Altium Designer)
    • New firmware for implantable pump and inductive charger (C, RTOS)
    • Design documentation
    • Creation of unit, functional, integration, and acceptance tests
    • Version and configuration management
  • Secure upload and storage of data in cloud
    • Requirements management
    • Implementation of secure (HTTPS, MQTTS) upload of data from external charger
    • ?Supplier selection of cloud service provider
  • Support in project management
  • Support in FDA audits
Aktives Implantat
Sequana Medical NV
Zurich (Switzerland)
4 Jahre 1 Monat
2019-07 - 2023-07

Product development of implantable and external components

Project management, Requirements management, Firmware development, Hardware development, Risk management, Design Documentation, Testing IEC 60601 DIN 13485 IEC 62304 ...
Project management, Requirements management, Firmware development, Hardware development, Risk management, Design Documentation, Testing
Product development of implanted and external components for an fully implantable heart support device (Class III, active implant)
  • Responsible for all activities for the product development of all external, patient-worn components
  • Responsible for all power and communication related components of the implant
  • Responsible for system to upload data from implant to a central data server
  • Development of firmware for above mentioned components (C, RTOS)
  • Development of application and server software using (C#/.Net)
  • Development of electronics for above mentioned components (Altium Designer, Spice)
  • Support for development of mechanics (SolidWorks)
IEC 60601 DIN 13485 IEC 62304 Requirements Requirements Management ALM Lifecycle Management Softwarearchitektur Schaltplan Layout Aktives Implantat
Syntach AB
Lund (Sweden)
1 Jahr 8 Monate
2021-10 - 2023-05

Test systems ? extracorporeal heart pump

Software development, documentation, testing
Software development, documentation, testing
Development of a test system for an extracorporal heart pump
  • Development of firmware for ARM (C)
  • Development of application test software (C#/.Net)
  • Creation of the integration and acceptance tests
  • Design documentation
Livanova
Pittsburgh (USA)
1 Jahr 2 Monate
2021-07 - 2022-08

wireless power transfer for an active neuro- or cranial implant

Electronics development, Coordination of suppliers, Prototype testing
Electronics development, Coordination of suppliers, Prototype testing
Development of a wireless energy transmission system for an active neuro/ cranial implant.
  • Development of power sender and receiver electronics (Altium Designer)
  • Selection and Management of suppliers
  • Creation of verification tests
  • Design documentation
Longeviti Neuro Solutions
Baltimore (USA)
3 Jahre 1 Monat
2017-04 - 2020-04

Electronics and firmware for automotive torque measuring instruments

Software development, Electronics development, documentation, testing
Software development, Electronics development, documentation, testing
Development of electronics and firmware for torque measurement devices located in cars
  • Development of 
    • firmware (C, Atmel Studio)
    • application test software (C#/.Net)
    • ?electronics (Altium Designer)
  • Definition and implementation of unit, integration and acceptance tests
Axon System GmbH
Inning (Germany)
8 Jahre 2 Monate
2010-12 - 2019-01

Establishing and managing the development department

Chief Technical Officer (CTO) since March 2012, previously Head of Development in Software & Electrical Engineering
Chief Technical Officer (CTO) since March 2012, previously Head of Development in Software & Electrical Engineering
Development and management of the development department, Monitoring of all development activities and project management, Technical Company representative towards customers, investors and suppliers
  • Coordination of all development projects
  • Allocation of resources and budgets in collaboration with the project leaders
  • Assist project leaders in planning development tasks
  • Definition of staff goals, tracking the defined goals, staff training
  • Definition of internal development and quality standards in software-, electrical- and mechanical engineering
  • Planning and managing projects (> 5 million budget, > 15 employees)
  • Hands-on focus on software development and electrical engineering
  • Internal audits and external audits
  • Support in risk management
DUALIS MedTech GmbH
Seefeld (Germany)
3 Jahre 8 Monate
2014-07 - 2018-02

Development, production and distribution of the NeoCare baby monitor

Chief Executive Officer (CEO), Founder, Shareholder
Chief Executive Officer (CEO), Founder, Shareholder
Development, production and sales of NeoCare baby monitor, the next generation baby monitor including vital sign tracking.
  • Building up company from scratch
  • Oversee all software development activities.
  • Software and algorithm development
  • Big data and cloud storage
  • Responsible for all sales and investor related activities
on request
Wessling (Germany)
3 Jahre 3 Monate
2007-12 - 2011-02

Further development of comprehensive network and file management software

Consultant in software development
Consultant in software development
Further development of a comprehensive network and file management software for the mainframe BS 2000 and Unix derivatives. Further development of a comprehensive text, hex and binary editor for Dos, Windows and Unix
  • Conception and development of APIs.
  • Development of test environments
  • Implementation of customer requirements
OPG ? Online Programmierung GmbH
Munich (Germany)
3 Jahre 3 Monate
2007-10 - 2010-12

Project management, Quality Management consulting, Regulatory affairs, Software development, IT consulting

Project management, company strategy consulting, implementation, and monitoring of a quality management system according to EN ISO 13485: 2003/ AC: 2009, development of approval strategies for active implants, software development, support of the IT infrastructure
  • Definition of project goals from the requirements
  • Project planning and structuring
  • Risk assessments, cost planning, resource planning
  • Project implementation and follow-up, technical guidance of assigned employees
  • Project Reviews
  • Planning, design and partial implementation of an infrastructure for storing patient data in cloud storage, big data
  • Planning, design and development of a web-based frontend to view patient data (GWT and Java) and Windows clients (C ++ / C #)
  • Planning, conception and partial development of software for embedded systems (ARM, Windows / Linux, ASM / C / C ++), control of data buses (CAN / SPI / SSP / I2C / UART, USB) for the connection of peripherals (Bluetooth, MICS , Displays, buttons, ...)
  • Development, implementation and monitoring of quality management systems and training in accordance with EN ISO 13485
  • Implementation of risk management
  • Supervision of external audits and internal audits
  • Regulatory affairs, cooperation with notified bodies
DUALIS MedTech GmbH
Seefeld (Germany)
4 Jahre 5 Monate
2004-08 - 2008-12

Development of complex computer games and other consumer entertainment products for PC and console

Chief Executive Officer (CEO), Chief Technical Officer (CTO), Founder, Shareholder Windows ASM / C / C ++ / C # openGL / DirectX
Chief Executive Officer (CEO), Chief Technical Officer (CTO), Founder, Shareholder
  • Lead game engine programmer
  • Development of a computer game based on a specially developed 3D engine and middleware
  • Negotiations with publishers and other investors
  • Public relation
  • Budget controlling, reporting, project management
Windows ASM / C / C ++ / C # openGL / DirectX
on request
Wuppertal (Germany)
1 Jahr 1 Monat
2006-10 - 2007-10

Project management, development of software for different mechatronic systems

Conception and development of hardware-related software.
  • Control of various displays, input devices and radio modules for a control and monitoring handheld for an artificial sphincter implant (ARM7, ASM / C).
  • Development of monitoring and evaluation software for in vivo tests
  • Design and EMC simulation of an antenna for implants (402-406 MHz).
  • Development of a motor controller for brushless motors.
  • Control based on various sensors and physiological values.
  • Design of evaluation boards.
German Aerospace Center (DLR)
Oberpfaffenhofen (Germany)

Aus- und Weiterbildung

Aus- und Weiterbildung

4 Jahre 9 Monate
2001-10 - 2006-06

Study of Computer Science

Diploma, Technical University of Munich
Diploma
Technical University of Munich
Main focus technical computer science and electrical engineering

Position

Position

  • Senior Medical Device Consultant in R&D, Regulatory and Team Management
  • Senior Engineering Consultant im Bereich Firmware, Hardware und Software Entwicklung, mit Schwerpunkt Medizintechnik

Kompetenzen

Kompetenzen

Top-Skills

Embedded Systems Projektmanagement/Projektleitung Embedded Software DIN 13485 IEC 60601 IEC 62304 ISO 14971 FDA Medizinprodukte Healthcare Schaltplan Layout Softwarearchitektur Requirements Engineering Testautomatisierung Lifecycle Management ALM Versionsverwaltung Azure Devops Firmware Hardware-Design

Schwerpunkte

  • Firmware/ Software development for medical devices
    • Conception and Definition of software requirements
    • Architectural design, design documentation, software risk management
    • Implementation
    • Unit testing, verification and integration testing
  • Electrical Engineering for medical devices
    • Conception and Definition of hardware requirements
    • Schematics and Layout, Hardware design documentation and FMEA
    • Verification and Integration testing
    • Transition to manufacturing
  • Project Management
    • Definition of project goals, planning and control
    • Development and introduction of project management processes
    • Release, change and configuration management
  • Team leadership
    • Building and disciplinary leadership of teams
    • Communication, motivation, and conflict resolution
    • Mentoring with hands-on mentality
  • Quality management
    • Development of new and optimization of existing quality processes
    • Carrying out internal audits and supporting external audits
  • Regulatory Affairs
    • ?Support for creation of design dossier for submissions

Produkte / Standards / Erfahrungen / Methoden

Skills
  • ALM & PM Tools
    • Jira, Perforce Helix ALM, Trac, MS Project
  • Versoning & CI Tools
    • Azure Devops, GIT, Jenkins, Subversion
  • Standards (extract)
    • Medical device software ? Software life cycle processes (IEC 62304)
    • Medical devices - Quality management systems (ISO 13485)
    • Medical devices - Application of risk management to medical devices (ISO 14971)
    • Medical electrical equipment (IEC 60601),
    • Medical devices - Application of usability engineering (IEC 62366)
  • Operating Systems and SDKs
    • Windows, Linux, WSL, ThreadX, TI RTOS, FreeRTOS, Keil RTOS, QF Framework, Azure and AWS
  • Hardware Systems
    • ARM / Cortex Controllers, MSP430, AVR, 8051, Intel X86/X64, iPhone, Android
  • Bus Systems
    • Ethernet, CAN, CANFD, SPI, SSP, I2C, UART, 1-Wire, USB, USB-PD, ?
  • Wireless Systems
    • WLAN, Bluetooth, 433/868 MHz, MICS, MedRadio, ZigBee, NFC
  • Software IDEs
    • VS Code, Eclipse IDEs, Keil uVision, Visual Studio, IAR Workbench, AVR Suite, Labview,
  • Hardware EDA
    • Altium Designer, Eagle, Spice
  • Mechanical Tools
    • Solidworks

Professional experience

2001 - today
Firmware/ Software development

2006 - today
Electrical Engineering

2007 - today
Project management and Quality and Regulatory Affairs

2010 - today
R&D Management since 2010

Programmiersprachen

  • C
  • C++
  • C#
  • Objective-C
  • Java
  • Assembler
  • LabVIEW
  • Python
  • HTML
  • CSS
  • Javascript

Branchen

Branchen

Umfangreiche Erfahrung im regulativen Umfeld der Medizintechnik. Betreuung der Kunden bei internen und externen Audits durch FDA & benannte Stelle

Vertrauen Sie auf Randstad

Im Bereich Freelancing
Im Bereich Arbeitnehmerüberlassung / Personalvermittlung

Fragen?

Rufen Sie uns an +49 89 500316-300 oder schreiben Sie uns:

Das Freelancer-Portal

Direktester geht's nicht! Ganz einfach Freelancer finden und direkt Kontakt aufnehmen.