We, livetec Ingenieurbüro GmbH are a young, innovative, growing company in the field of medical technology (cardiology, elektrophysiology, heart surgery, laser therapy) and are looking for motivated, creative and innovative thinking employees (m/f/d), who want to shape the future with us.
Electronics technician or state-certified technician - specialisation: devices & systems or similar (m/f/d)
Your tasks:
- Production of livetec products, including cardiology/electrophysiology, in accordance with the currently valid QM system EN ISO 13485:2016 (MDR).
- Production and testing of assemblies & complete devices according to the corresponding production regulations
- Qualified service, repair and safety-related control of equipment returns (internal/external)
Your profile:
- With work experience or career starter
- Good MS Office & computer skills
Experience with software-measurement tools, as well as with common manufacturing processes
- Independent & result-oriented work, communication skills, ability to work in a team, confident appearance
Further information:
- Full-time, part-time - flexible
- Wanted immediately
- Unlimited employment relationship
Quality Manager (m/f/d) Medical Technology
Your tasks:
- Maintenance of our quality management system (QMS) according to EN ISO 13485
- Optimization and improvement of the QMS according to new MDR
- Support of the management in the context of processes and requirements (management report)
- Conception, execution and monitoring of internal and external audits
- Maintenance of the QMS manual, document creation, document maintenance and archiving
- Report to the management: e.g. innovations regulatory requirements
Improvements of the QM system regarding product maintenance, product development, product approvals and profitability
- QA / Vigilance / Post Market Surveillance
- Support RA, development and production within the framework of the QMS
- Training of employees regarding quality management requirements
- Communication with Notified Bodies
- Direct cooperation with the PRRC
Your profile:
- Medical technology training/studies or equivalent QM-oriented training/studies
- Desirable/advantageous experience in the field of ISO 13485
- Good German and English language skills
- Desirable/advantageous knowledge of international norms and standards e.g. EN ISO 60601-1
Further Information:
- Full-time or part-time - variable
- Wanted immediately
- Open-ended contract of employment
Electronics technician or state-certified technician - specialisation: devices & systems or similar (m/f/d)
Your tasks:
- Production of livetec products, including cardiology/electrophysiology, in accordance with the currently valid QM system EN ISO 13485:2016 (MDR).
- Production and testing of assemblies & complete devices according to the corresponding production regulations
- Qualified service, repair and safety-related control of equipment returns (internal/external)
Your profile:
- With work experience or career starter
- Good MS Office & computer skills
Experience with software-measurement tools, as well as with common manufacturing processes - Independent & result-oriented work, communication skills, ability to work in a team, confident appearance
Further information:
- Full-time, part-time - flexible
- Wanted immediately
- Unlimited employment relationship
Quality Manager (m/f/d) Medical Technology
Your tasks:
- Maintenance of our quality management system (QMS) according to EN ISO 13485
- Optimization and improvement of the QMS according to new MDR
- Support of the management in the context of processes and requirements (management report)
- Conception, execution and monitoring of internal and external audits
- Maintenance of the QMS manual, document creation, document maintenance and archiving
- Report to the management: e.g. innovations regulatory requirements
Improvements of the QM system regarding product maintenance, product development, product approvals and profitability - QA / Vigilance / Post Market Surveillance
- Support RA, development and production within the framework of the QMS
- Training of employees regarding quality management requirements
- Communication with Notified Bodies
- Direct cooperation with the PRRC
Your profile:
- Medical technology training/studies or equivalent QM-oriented training/studies
- Desirable/advantageous experience in the field of ISO 13485
- Good German and English language skills
- Desirable/advantageous knowledge of international norms and standards e.g. EN ISO 60601-1
Further Information:
- Full-time or part-time - variable
- Wanted immediately
- Open-ended contract of employment