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Design Quality Engineer
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Design, Engineering, Engineer
Projektbeschreibung
Your duties and responsibilities:
- Within the Design Quality team you're focusing on life cycle management activities
- You're enhancing the Design Control and Risk Management processes to better reflect state of the art practices and drive continuous improvement
- You're applying statistical methods and processing/designing excellence tools to establish test plans as well as evaluate test data and processes. Perform Gage R&R studies
- You' re providing leadership in all areas of the Quality System, including, but not limited to Corrective & Preventive Actions, Complaints, Nonconforming Materials, Risk Management, etc
- You're providing leadership in the understanding of medical device regulations to other disciplines
- You know and follow all laws and policies that apply to the job, and maintain the highest levels of professionalism, ethics and compliance at all times
What we require:
- A minimum of a Bachelor's degree in Engineering or related technical or scientific discipline with a minimum of 7+ years of experience in related field is required
- Proven exceptional written and oral presentation skills
- Working knowledge of Design Controls, GMPs, QSR, 21 CFR 820, MDD 93/42/EEC, ISO13485 and ISO14971 quality requirements is required
- Previous Quality Engineering experience is preferred
- Experience in a Medical Device regulated environment
- Fluency in English is required, good knowledge of German would be a strong asset
We offer you a competitive salary and an interesting challenge in a well named company which will benefit your career.
If you are the person we're looking for please submit your application. We're looking forward to getting to know you.
- Within the Design Quality team you're focusing on life cycle management activities
- You're enhancing the Design Control and Risk Management processes to better reflect state of the art practices and drive continuous improvement
- You're applying statistical methods and processing/designing excellence tools to establish test plans as well as evaluate test data and processes. Perform Gage R&R studies
- You' re providing leadership in all areas of the Quality System, including, but not limited to Corrective & Preventive Actions, Complaints, Nonconforming Materials, Risk Management, etc
- You're providing leadership in the understanding of medical device regulations to other disciplines
- You know and follow all laws and policies that apply to the job, and maintain the highest levels of professionalism, ethics and compliance at all times
What we require:
- A minimum of a Bachelor's degree in Engineering or related technical or scientific discipline with a minimum of 7+ years of experience in related field is required
- Proven exceptional written and oral presentation skills
- Working knowledge of Design Controls, GMPs, QSR, 21 CFR 820, MDD 93/42/EEC, ISO13485 and ISO14971 quality requirements is required
- Previous Quality Engineering experience is preferred
- Experience in a Medical Device regulated environment
- Fluency in English is required, good knowledge of German would be a strong asset
We offer you a competitive salary and an interesting challenge in a well named company which will benefit your career.
If you are the person we're looking for please submit your application. We're looking forward to getting to know you.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Ingenieurwesen/Technik