Description
Quality Engineer (m/f)
Reference: -en
Start: 10/18
Duration: 7 MM++
Main tasks:
- Support and improve quality system management in compliance with applicable requirements (ISO 9001, ISO 13485, QSR 21 CFR 820)
- Promote continuous improvement process (non-conformity, CAPA and change management)
- Support dental R&D project and improvement project from quality perspective specially for risk management process and any quality impact on design process
- Participate in third parties audits (bodies notified, authorities, ISO 13485, FDA)
- Manage the Continuous Improvement Plan
- Promote quality system and approach within the company
Main qualifications
- Degree in Quality Engineering or equivalent
- Profound experience in Quality Engineering in the pharmaceutical industry
- Knowledge of the requirements relative to the ISO13485, European directive 93/42 and 21 CFR part 820
- Good communication and coordination skills
- Knowledge of the usual computing tools
- Fluent in English and French
Main advantages:
- Interesting tasks in a multinational environment
- Good infrastructure
- Support throughout the entire application process
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Veronika Walz
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