Beschreibung
Compliance Auditor JNJKJP (m/f)
Reference: -en
Start: 02/19
Duration: 9 MM+
Main tasks:
- Conduction of internal audits according 21 CFR 820; ISO EN 13485:2016; MDD; other applicable regulations
- Writing of internal and reports and creation of relevant documentation
- Follow up of internal and external audit observation to assure appropriate and timely implementation of Corrective Actions
- Provide Regulatory Compliance support in all areas of Quality System Elements
- Documentation review in Quality System relevant areas
Main qualifications
- Master’s degree in a technical or scientific discipline
- Proven exceptional written and oral presentation skills
- Working knowledge of applicable regulations
- Experience in an Medical Device regulated environment
- Strong knowledge and skills in MS Office
- Excellent problem solving, decision-making, and root cause analysis skills are required
- Interpersonal skills that foster conflict resolution are required
- Ability to multi-task independently with minimal supervision
- Fluency in English is required, good knowledge of German would be a strong asset
Main advantages:
- A very renowned company
- You will work in an international environment
- Dynamic and innovative market environment
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.
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