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Development Engineer
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Engineering, Design, Engineer, Cad
Projektbeschreibung
For our client in OBERDORF we are looking for a DEVELOPMENT ENGINEER for a 13-MONTH contract.
JOB TITLE: DEVELOPMENT ENGINEER
DURATION: 15/11/2018 TO 31/12/2019
LOCATION: OBERDORF
WORKLOAD: 100%
DESCRIPTION:
Development Engineer - Sustaining Engineering (Daily Business) - is responsible for the design, development and documentation of existing electromechanical medical devices. Can work on independently complex assignments.
RESPONSIBILITIES:
- Is contact person for internal and external technical questions/issues of products on market
- Designs, develops and improves electromechanical medical devices according to the Synthes product development/change process
- Investigation of issues of products on market (NC, SCAR, CAPA, Complaint)
- Performs the required activities and generates the appropriate technical documents to ensure compliance with national and international regulations related to medical devices (EU MDD/MDR, US FDA, Japanese PAL)
- Works with manufacturing during the design stages to incorporate manufacturability into the product designs and during the implementation phase
- Works with internal shared services (Design Engineering, Quality, Regulatory) and external suppliers to achieve agreed project milestones (eg For supplier Change Requests, Design Changes)
- Develops with the test team test set-ups (including derivation of benchmarks) and coordinates the activities required to fabricate test parts and - complete testing (according to PD process)
- Knowledge and compliance with laws and policies that apply to the job and ensure a high level of professionalism, ethics and compliance at all time
MUST HAVES:
- Master/bachelor's degree in mechanical or mechatronics engineering
- At least 2 years of experience in the design and development of medical devices or comparable industries
- Business fluent in German and good knowledge of English
- Creative/problem-solving skills
- CAD knowledge preferably PTC Creo
- Good documentation practice (GDP) knowledge
- Analytical skills
- Willingness to accept responsibility
- Team player
NON-TECHNICAL PROFILE REQUIREMENTS:
- Some flexibility in working hours is required - Must be able to work on multiple simultaneous tasks with limited supervision;
- Quick learner, motivated self-starter;
- Excellent customer service, interpersonal, communication and team collaboration skills;
- Able to follow change management for internal guidelines.
- English and German spoken and written;
For further details please contact:
Anna Undas
(see below)
JOB TITLE: DEVELOPMENT ENGINEER
DURATION: 15/11/2018 TO 31/12/2019
LOCATION: OBERDORF
WORKLOAD: 100%
DESCRIPTION:
Development Engineer - Sustaining Engineering (Daily Business) - is responsible for the design, development and documentation of existing electromechanical medical devices. Can work on independently complex assignments.
RESPONSIBILITIES:
- Is contact person for internal and external technical questions/issues of products on market
- Designs, develops and improves electromechanical medical devices according to the Synthes product development/change process
- Investigation of issues of products on market (NC, SCAR, CAPA, Complaint)
- Performs the required activities and generates the appropriate technical documents to ensure compliance with national and international regulations related to medical devices (EU MDD/MDR, US FDA, Japanese PAL)
- Works with manufacturing during the design stages to incorporate manufacturability into the product designs and during the implementation phase
- Works with internal shared services (Design Engineering, Quality, Regulatory) and external suppliers to achieve agreed project milestones (eg For supplier Change Requests, Design Changes)
- Develops with the test team test set-ups (including derivation of benchmarks) and coordinates the activities required to fabricate test parts and - complete testing (according to PD process)
- Knowledge and compliance with laws and policies that apply to the job and ensure a high level of professionalism, ethics and compliance at all time
MUST HAVES:
- Master/bachelor's degree in mechanical or mechatronics engineering
- At least 2 years of experience in the design and development of medical devices or comparable industries
- Business fluent in German and good knowledge of English
- Creative/problem-solving skills
- CAD knowledge preferably PTC Creo
- Good documentation practice (GDP) knowledge
- Analytical skills
- Willingness to accept responsibility
- Team player
NON-TECHNICAL PROFILE REQUIREMENTS:
- Some flexibility in working hours is required - Must be able to work on multiple simultaneous tasks with limited supervision;
- Quick learner, motivated self-starter;
- Excellent customer service, interpersonal, communication and team collaboration skills;
- Able to follow change management for internal guidelines.
- English and German spoken and written;
For further details please contact:
Anna Undas
(see below)
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik