Description
My Client is one of the largest Pharmaceutical Manufacturers worldwide. With around 20´000 employees he is expanding and currently seeking a CSV - Computer System Validation Specialist on a fixed contract basis (freelancer) in the area Medical Devices.Requirements:
- Creation of the validation documentation for the GxP relevant system elements
- Medical device and/or pharmaceutical experience are preferred.
- Responsible for supporting Computer Systems Compliance activities applicable to country specific regulations (e.g. FDA), international standards (e.g. ISO) and as appropriate best business practices (e.g. GAMP 5). This includes the creation, execution and coordination of GxP computer system validation activities.
- You have to be experienced in national and international regulations and standards FDA QSR, 21 CFR Part 820, Part 11, GAMP5, ISO 13485, ISO 62304
Would you be interested to work in an international and future-oriented team, in which you could contribute and expand your experience? If you are flexible and you have a good communication and team-work skills, you can expect an interesting, varied work with contacts to partners overseas. My client appreciates a quick learner and a motivated self-starter. For this role you bring an IT background and higher education (Engineer or similar) and you have a minimum of 3 years experience in Computer System Validation.
Languages: English and German fluent in speaking and writing
Duration: ASAP for 8 months
Location: North-West Switzerland (German part speaking)
You feel that this project is something for you, then you can expect a challenging and varied job in a multicultural environment. Please send me your complete application documents , you can also call me on , I am looking forward to hearing about your current status, and to discuss any other vacancy.
Best Regards from Zurich
Magda Arnold
I am a recruitment consultant specialized in the area Medical Devices.
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