Job Description:
Concept development
Performance assessment of used platform
Coordination of implemented features with project leader
Development of embedded firmware in C/C++ and assembler in collaboration with hard- and software engineers
Documentation of product development according to the internal quality system und regulatory requirements
Active collaboration in quality management
Maintenance and servicing of embedded firmware
Collaboration during system integration
System modelling and simulation
Verification and validaton
Qualification and skills:
Several years of experience with embedded C/C++ and assembler
Knowledge of real-time operating systems and real-time applications
Knowledge of debugging multitasking/multicore real-time applications
Knowledge of serial bus formats and interfaces (RS232, USB, I2C, SPI)
Establishing a development environment with compile, assembler, debugger, emulator
Knowledge of synchronous/asynchronous logic design
Knowledge of Linux, if possible in the area embedded systems
Knowledge of and experience with UML and SysML an asset
Good knowledge of signal processing an asset
Communicative personality and team player
Self-reliant, proactive, systematic and structured working method
Inquisitiveness and willingness to learn
Self-dependent team player
Very good written and spoken English and German
MED-EL is a fast pace and high-tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com. We look forward to receiving your application via e-mail to: jobs@medel.com.
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
Showing posts with label Austria. Show all posts
Showing posts with label Austria. Show all posts
Wednesday, January 6, 2010
Regulatory Affairs Manager - MED-EL Elektromedizinische Geräte GmbH - Innsbruck - Austria
Job Description:
The Regulatory Affairs Manager is the primary contact person for development, preparation, and submission of product approval applications and notifications to regulatory agencies and governing bodies for all products produced and/or distributed by our company.
As a working manager, the RA Manager provides, or directs other RA personnel to provide, input to product development projects regarding regulatory strategy, regulatory requirements and related company requirements.
The RA Manager is responsible for assuring that all procedural requirements of the Corporate Regulatory Affairs Department in Innsbruck are fulfilled and provides input to global regulatory strategies and policies.
Qualification and skills:
Working experience (approx 5 years) with medical devices regulatory submissions for approvals and registrations which meet the requirements of MDD, AIMD, FDA, Health Canada, MHLW, sFDA, etc. Must compile regulatory submissions; a do´er plus a team leader.
Expert level of knowledge of EU, US FDA, Canadian, Japan, China, Korea regulatory requirements and submissions process.
Ability to formulate regulatory strategies for global market approvals and present them to Senior Management.
Demonstrated leadership of a regulatory team. Manage task assignments and status reviews.
Demonstrated organization skills to manage all aspects of regulatory affairs on a daily basis. Includes interface with Senior Management, R&D, Marketing, Product Management, etc.
Experience and capability to interface with Subsidiaries and Sales Offices regarding regulatory questions.
Knowledge of and experience with regulatory requirements for clinical studies.
Knowledge of regulatory requirements for labelling and country language requirements.
Ability to be the primary interface with US FDA and TÜV regarding pre-submissions discussions, submissions, and post-submission resolution of questions.
Professionalism and seniority to represent the company at conferences, technical meetings, and association meetings.
MED-EL is a fast pace and high-tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com. We look forward to receiving your application via e-mail to: jobs@medel.com.
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
The Regulatory Affairs Manager is the primary contact person for development, preparation, and submission of product approval applications and notifications to regulatory agencies and governing bodies for all products produced and/or distributed by our company.
As a working manager, the RA Manager provides, or directs other RA personnel to provide, input to product development projects regarding regulatory strategy, regulatory requirements and related company requirements.
The RA Manager is responsible for assuring that all procedural requirements of the Corporate Regulatory Affairs Department in Innsbruck are fulfilled and provides input to global regulatory strategies and policies.
Qualification and skills:
Working experience (approx 5 years) with medical devices regulatory submissions for approvals and registrations which meet the requirements of MDD, AIMD, FDA, Health Canada, MHLW, sFDA, etc. Must compile regulatory submissions; a do´er plus a team leader.
Expert level of knowledge of EU, US FDA, Canadian, Japan, China, Korea regulatory requirements and submissions process.
Ability to formulate regulatory strategies for global market approvals and present them to Senior Management.
Demonstrated leadership of a regulatory team. Manage task assignments and status reviews.
Demonstrated organization skills to manage all aspects of regulatory affairs on a daily basis. Includes interface with Senior Management, R&D, Marketing, Product Management, etc.
Experience and capability to interface with Subsidiaries and Sales Offices regarding regulatory questions.
Knowledge of and experience with regulatory requirements for clinical studies.
Knowledge of regulatory requirements for labelling and country language requirements.
Ability to be the primary interface with US FDA and TÜV regarding pre-submissions discussions, submissions, and post-submission resolution of questions.
Professionalism and seniority to represent the company at conferences, technical meetings, and association meetings.
MED-EL is a fast pace and high-tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com. We look forward to receiving your application via e-mail to: jobs@medel.com.
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
Regulatory Affairs Specialist - MED-EL Elektromedizinische Geräte GmbH - Innsbruck - Austria
Job Description:
The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned.
Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements.
Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle.
Reports to Manager, Regulatory Affairs
Qualification and skills:
knowledge and demonstrated proficiency in the field of Regulatory Affairs andmedical device
perfect English verbal and written skills necessary
very good German skills preferred
must be team-oriented
project management skills necessary to be successful
negotiation skills necessary to be successful
MED-EL is a fast pace and high-tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com. We look forward to receiving your application via e-mail to: jobs@medel.com.
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned.
Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements.
Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle.
Reports to Manager, Regulatory Affairs
Qualification and skills:
knowledge and demonstrated proficiency in the field of Regulatory Affairs andmedical device
perfect English verbal and written skills necessary
very good German skills preferred
must be team-oriented
project management skills necessary to be successful
negotiation skills necessary to be successful
MED-EL is a fast pace and high-tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com. We look forward to receiving your application via e-mail to: jobs@medel.com.
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
Sunday, August 9, 2009
Senior Engineer Predevelopment Dimming Ballasts - TridonicAtco GmbH And Co KG - Dornbirn - Austria
Responsibilities:
It is your competency to define the overall technology strategy and the state of the art in research & technology.
You create new topologies and methods and ensure the reliability and manufacturing process compatibility.
You are responsible for the technical system design and continuous improvement in the design process.
The presentation of results and concepts to steering committees as well as coordination of activities with other departments are part of your function.
Requirements:
University degree in electrical engineering or an equivalent study.
Industrial experience in system design and basic understanding in project management is a plus.
Networked and systematic thinking as well as strong ability to understand systems and its interaction is your strength.
You look forward to using your English language skills in international teams.
Welcome!
To apply for this position, please send your CV and cover letter via our online recruiting tool:
TridonicAtco GmbH & Co KG
Judith Zortea
Human Resources Specialist
Tel. +43 5572 395-4596
Fax +43 5572 395-94596
jobs@tridonicatco.com
Apply at: www.tridonicatco.com
It is your competency to define the overall technology strategy and the state of the art in research & technology.
You create new topologies and methods and ensure the reliability and manufacturing process compatibility.
You are responsible for the technical system design and continuous improvement in the design process.
The presentation of results and concepts to steering committees as well as coordination of activities with other departments are part of your function.
Requirements:
University degree in electrical engineering or an equivalent study.
Industrial experience in system design and basic understanding in project management is a plus.
Networked and systematic thinking as well as strong ability to understand systems and its interaction is your strength.
You look forward to using your English language skills in international teams.
Welcome!
To apply for this position, please send your CV and cover letter via our online recruiting tool:
TridonicAtco GmbH & Co KG
Judith Zortea
Human Resources Specialist
Tel. +43 5572 395-4596
Fax +43 5572 395-94596
jobs@tridonicatco.com
Apply at: www.tridonicatco.com
Tuesday, July 28, 2009
Senior Engineer - TridonicAtco GmbH And Co KG - Dornbirn - Austria
Responsibilities:
It is your competency to define the overall technology strategy and the state of the art in research & technology.
You create new topologies and methods and ensure the reliability and manufacturing process compatibility.
You are responsible for the technical system design and continuous improvement in the design process.
The presentation of results and concepts to steering committees as well as coordination of activities with other departments are part of your function.
Requirements:
University degree in electrical engineering or an equivalent study.
Industrial experience in system design and basic understanding in project management is a plus.
Networked and systematic thinking as well as strong ability to understand systems and its interaction is your strength.
You look forward to using your English language skills in international teams.
Welcome!
To apply for this position, please send your CV and cover letter via our online recruiting tool:
TridonicAtco GmbH & Co KG
Judith Zortea
Human Resources Specialist
Tel. +43 5572 395-4596
Fax +43 5572 395-94596
jobs@tridonicatco.com
Apply at: www.tridonicatco.com
It is your competency to define the overall technology strategy and the state of the art in research & technology.
You create new topologies and methods and ensure the reliability and manufacturing process compatibility.
You are responsible for the technical system design and continuous improvement in the design process.
The presentation of results and concepts to steering committees as well as coordination of activities with other departments are part of your function.
Requirements:
University degree in electrical engineering or an equivalent study.
Industrial experience in system design and basic understanding in project management is a plus.
Networked and systematic thinking as well as strong ability to understand systems and its interaction is your strength.
You look forward to using your English language skills in international teams.
Welcome!
To apply for this position, please send your CV and cover letter via our online recruiting tool:
TridonicAtco GmbH & Co KG
Judith Zortea
Human Resources Specialist
Tel. +43 5572 395-4596
Fax +43 5572 395-94596
jobs@tridonicatco.com
Apply at: www.tridonicatco.com
Sunday, July 12, 2009
Medical Writer - MED-EL Elektromedizinische Geräte GmbH - Innsbruck - Austria
Responsibilities:
To research, create, edit and proofread documents in English to the highest standard for a full range of medical education and communications materials such as scientific articles, abstracts, posters, press releases, brochures, and oral presentations
Working with teams within MED-EL as well as teams located at various clinics using our products
Qualification and skills:
Degree in sciences or social sciences
Medical writing experience preferably in the medical device industry
Demonstrated understanding of clinical research
A flexible attitude about work assignments and new learning
Team player
Good interpersonal skills, negotiation, has an eye for detail
Verbal and written communication skills
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We offer you a multifaceted challenge in our globally acting company with a multinational working atmosphere and English as the company language. Our Head Office in Innsbruck offers you a high quality of life in an attractive environment. We look forward to receiving your application via e-mail to: jobs@medel.com .
To research, create, edit and proofread documents in English to the highest standard for a full range of medical education and communications materials such as scientific articles, abstracts, posters, press releases, brochures, and oral presentations
Working with teams within MED-EL as well as teams located at various clinics using our products
Qualification and skills:
Degree in sciences or social sciences
Medical writing experience preferably in the medical device industry
Demonstrated understanding of clinical research
A flexible attitude about work assignments and new learning
Team player
Good interpersonal skills, negotiation, has an eye for detail
Verbal and written communication skills
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We offer you a multifaceted challenge in our globally acting company with a multinational working atmosphere and English as the company language. Our Head Office in Innsbruck offers you a high quality of life in an attractive environment. We look forward to receiving your application via e-mail to: jobs@medel.com .
Regulatory Affairs Specialist - MED-EL Elektromedizinische Geräte GmbH - Innsbruck - Austria
Job Description:
The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned
Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements
Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle
Reports to Manager, Regulatory Affairs
Qualification and skills:
Knowledge and demonstrated proficiency in the field of Regulatory Affairs and medical device
Perfect English skills necessary
Very good German skills preferred
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We look forward to receiving your application via e-mail to: jobs@medel.com .
The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned
Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements
Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle
Reports to Manager, Regulatory Affairs
Qualification and skills:
Knowledge and demonstrated proficiency in the field of Regulatory Affairs and medical device
Perfect English skills necessary
Very good German skills preferred
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We look forward to receiving your application via e-mail to: jobs@medel.com .
Tuesday, June 30, 2009
Senior Engineer - TridonicAtco GmbH And Co KG - Dornbirn - Austria
Responsibilities:
It is your competency to define the overall technology strategy and the state of the art in research & technology.
You create new topologies and methods and ensure the reliability and manufacturing process compatibility.
You are responsible for the technical system design and continuous improvement in the design process.
The presentation of results and concepts to steering committees as well as coordination of activities with other departments are part of your function.
Requirements:
University degree in electrical engineering or an equivalent study.
Industrial experience in system design and basic understanding in project management is a plus.
Networked and systematic thinking as well as strong ability to understand systems and its interaction is your strength.
You look forward to using your English language skills in international teams.
Welcome!
To apply for this position, please send your CV and cover letter via our online recruiting tool:
TridonicAtco GmbH & Co KG
Judith Zortea
Human Resources Specialist
Tel. +43 5572 395-4596
Fax +43 5572 395-94596
jobs@tridonicatco.com
Apply at: www.tridonicatco.com
It is your competency to define the overall technology strategy and the state of the art in research & technology.
You create new topologies and methods and ensure the reliability and manufacturing process compatibility.
You are responsible for the technical system design and continuous improvement in the design process.
The presentation of results and concepts to steering committees as well as coordination of activities with other departments are part of your function.
Requirements:
University degree in electrical engineering or an equivalent study.
Industrial experience in system design and basic understanding in project management is a plus.
Networked and systematic thinking as well as strong ability to understand systems and its interaction is your strength.
You look forward to using your English language skills in international teams.
Welcome!
To apply for this position, please send your CV and cover letter via our online recruiting tool:
TridonicAtco GmbH & Co KG
Judith Zortea
Human Resources Specialist
Tel. +43 5572 395-4596
Fax +43 5572 395-94596
jobs@tridonicatco.com
Apply at: www.tridonicatco.com
Monday, June 29, 2009
Regulatory Affairs Specialist - MED-EL Elektromedizinische Geräte GmbH - Innsbruck - Austria
Job Description:
The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned
Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements
Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle
Reports to Manager, Regulatory Affairs
Qualification and skills:
Knowledge and demonstrated proficiency in the field of Regulatory Affairs and medical device
Perfect English skills necessary
Very good German skills preferred
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We look forward to receiving your application via e-mail to: jobs@medel.com .
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned
Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements
Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle
Reports to Manager, Regulatory Affairs
Qualification and skills:
Knowledge and demonstrated proficiency in the field of Regulatory Affairs and medical device
Perfect English skills necessary
Very good German skills preferred
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We look forward to receiving your application via e-mail to: jobs@medel.com .
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
Tuesday, June 23, 2009
Medical Writer - MED-EL Elektromedizinische Geräte GmbH - Innsbruck - Austria
Responsibilities:
To research, create, edit and proofread documents in English to the highest standard for a full range of medical education and communications materials such as scientific articles, abstracts, posters, press releases, brochures, and oral presentations
Working with teams within MED-EL as well as teams located at various clinics using our products
Qualification and skills:
Degree in sciences or social sciences
Medical writing experience preferably in the medical device industry
Demonstrated understanding of clinical research
A flexible attitude about work assignments and new learning
Team player
Good interpersonal skills, negotiation, has an eye for detail
Verbal and written communication skills
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We offer you a multifaceted challenge in our globally acting company with a multinational working atmosphere and English as the company language. Our Head Office in Innsbruck offers you a high quality of life in an attractive environment. We look forward to receiving your application via e-mail to: jobs@medel.com .
MED-EL Elektromedizinische Geräte GmbH
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
To research, create, edit and proofread documents in English to the highest standard for a full range of medical education and communications materials such as scientific articles, abstracts, posters, press releases, brochures, and oral presentations
Working with teams within MED-EL as well as teams located at various clinics using our products
Qualification and skills:
Degree in sciences or social sciences
Medical writing experience preferably in the medical device industry
Demonstrated understanding of clinical research
A flexible attitude about work assignments and new learning
Team player
Good interpersonal skills, negotiation, has an eye for detail
Verbal and written communication skills
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We offer you a multifaceted challenge in our globally acting company with a multinational working atmosphere and English as the company language. Our Head Office in Innsbruck offers you a high quality of life in an attractive environment. We look forward to receiving your application via e-mail to: jobs@medel.com .
MED-EL Elektromedizinische Geräte GmbH
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
Regulatory Affairs Specialist - MED-EL Elektromedizinische Geräte GmbH - Innsbruck - Austria
Job Description:
The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned
Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements
Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle
Reports to Manager, Regulatory Affairs
Qualification and skills:
Knowledge and demonstrated proficiency in the field of Regulatory Affairs and medical device
Perfect English skills necessary
Very good German skills preferred
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We look forward to receiving your application via e-mail to: jobs@medel.com .
MED-EL Elektromedizinische Geräte GmbH
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
The focal point for development, preparation, and submission of applications and notifications to international regulatory agencies and governing bodies, as assigned
Provides input to product development projects and changes to existing products regarding regulatory requirements and related company requirements
Provides input to the development of regulatory strategies and obtaining regulatory approvals from international regulatory agencies, as required throughout the product life cycle
Reports to Manager, Regulatory Affairs
Qualification and skills:
Knowledge and demonstrated proficiency in the field of Regulatory Affairs and medical device
Perfect English skills necessary
Very good German skills preferred
MED-EL is a fast pace and high tech company specialized in implantable medical devices. We design, fabricate, and distribute cochlear implants and other neuro stimulation products. The company is located in scenic Innsbruck, Austria. For more information check our website at www.medel.com.
We look forward to receiving your application via e-mail to: jobs@medel.com .
MED-EL Elektromedizinische Geräte GmbH
Worldwide Headquarters
Fürstenweg 77a
A-6020 Innsbruck
Austria
Tel: +43(0)512 288889
Fax: +43(0)512 293381
Senior Engineer - TridonicAtco GmbH And Co KG - Dornbirn - Austria
Responsibilities:
It is your competency to define the overall technology strategy and the state of the art in research & technology.
You create new topologies and methods and ensure the reliability and manufacturing process compatibility.
You are responsible for the technical system design and continuous improvement in the design process.
The presentation of results and concepts to steering committees as well as coordination of activities with other departments are part of your function.
Requirements:
University degree in electrical engineering or an equivalent study.
Industrial experience in system design and basic understanding in project management is a plus.
Networked and systematic thinking as well as strong ability to understand systems and its interaction is your strength.
You look forward to using your English language skills in international teams.
Welcome!
To apply for this position, please send your CV and cover letter via our online recruiting tool:
TridonicAtco GmbH & Co KG
Judith Zortea
Human Resources Specialist
Tel. +43 5572 395-4596
Fax +43 5572 395-94596
jobs@tridonicatco.com
Apply at: www.tridonicatco.com
The Zumtobel Group, with more than 7,700 employees worldwide, ranks among the leading international manufacturers of luminaires and lighting solutions, lighting management and lighting components for professional indoor and outdoor applications.Thorn, Zumtobel and TridonicAtco are brands belonging to the Zumtobel Group. Maximum customer focus, outstandingly qualified employees, a determination to innovate and strong corporate values will secure the future growth and success of the Zumtobel Group.
It is your competency to define the overall technology strategy and the state of the art in research & technology.
You create new topologies and methods and ensure the reliability and manufacturing process compatibility.
You are responsible for the technical system design and continuous improvement in the design process.
The presentation of results and concepts to steering committees as well as coordination of activities with other departments are part of your function.
Requirements:
University degree in electrical engineering or an equivalent study.
Industrial experience in system design and basic understanding in project management is a plus.
Networked and systematic thinking as well as strong ability to understand systems and its interaction is your strength.
You look forward to using your English language skills in international teams.
Welcome!
To apply for this position, please send your CV and cover letter via our online recruiting tool:
TridonicAtco GmbH & Co KG
Judith Zortea
Human Resources Specialist
Tel. +43 5572 395-4596
Fax +43 5572 395-94596
jobs@tridonicatco.com
Apply at: www.tridonicatco.com
The Zumtobel Group, with more than 7,700 employees worldwide, ranks among the leading international manufacturers of luminaires and lighting solutions, lighting management and lighting components for professional indoor and outdoor applications.Thorn, Zumtobel and TridonicAtco are brands belonging to the Zumtobel Group. Maximum customer focus, outstandingly qualified employees, a determination to innovate and strong corporate values will secure the future growth and success of the Zumtobel Group.
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