Sterilisation Expert, Medical Devices, Contract, Switzerland

STERILITY ASSURANCE SPECIALIST, NON-STERILE MEDICAL DEVICES, CONTRACT, SWITZERLAND

We have an exclusive Contract opportunity in the canton of Solothurn to lead the sterilisation and registration processes of a global medical device manufacturer for the European region. Our client offers a leading position for European sterility assurance activities and varied responsibilities within regulatory compliance and stakeholder management including the training of colleagues throughout their manufacturing environment. English is the only language requirement for the role, the position offers a competitive Hourly rate on a rolling 6 month Contract basis.

The position requires at least 5 years experience in clinical reprocessing (cleaning, disinfection and sterilization) of medical device.

We welcome applications of consultants' who match most of the above requirements and are available on a short notice. Please note there is a job description available on request and there is a likelihood of the contract extending into 2016.

We hope the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this email and I will endeavour to get back to you with further information on the role and answer any questions you may have.

Kind regards,

Neha Sharma

MBA Michael Bailey Associates

Job Code: 106392

Key words: Sterilisation, Mikrobiologe, microbiologist, Steril, medizinprodukt, freelancer, ISO, EN, CE, FDA, ETO, ISO 14971, ISO 13485, validation, compliance, regulatory engineer, bioengineer, regulatory compliance, Medical Device Directive, MDD, clinical reprocessing, EN ISO EN ISO 15883, EN ISO 17665, EN ISO 17664, RKI guideline, AAMI TIR 12, reprocessing program, non-sterile medical devices Michael Bailey International is acting as an Employment Business in relation to this vacancy.