Description
My Client is one of the largest Pharmaceutical Manufacturers worldwide. With around 20´000 employees he is expanding and currently seeking a Sterility Assurance Specialist on a fixed contract basis (freelancer) in the area Medical Devices. This role is critical to all documentation and procedures relating to the sterilization process to meet the exact standards that the company demands.Requirements:
- Medical device and/or pharmaceutical experience are preferred.
- You have to be experienced in national and international regulations (FDA, ISO 13485), sterilization standards (i.e. ISO/EN/AAMI standards) and microbiological control of medical devices as EN556 and AAMI TIR33, ISO , etc.
- Write documentation including Technical Files, Design Dossiers, manuals, forms, templates, procedures etc as required for regulatory compliance of customer's products.
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 organized and you have a good communication and team-work skills, you can expect an interesting, varied work with company's employees, subcontractors and suppliers at all levels.
My client appreciates a quick learner and a motivated self-starter. For this role you bring a degree in a Life Science discipline and at least more than 3 years experience in Quality Assurance.
Languages: Fluent in English and German
Duration: for nearly 8 months
Location: North-East of 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 CV to , 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.
Campaign Ref: CH
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