Sterility Assurance Specialist

Sterility Assurance Specialist - Zuchwill - 40 Hours per Week

For one of our client, specialized in medical devices based in Zuchwil (canton of Solothurn in Switzerland), we are looking for a STERILITY ASSURANCE SPECIALIST with experience in clinical reprocessing.

This is a challenging, CONTRACTING POSITION, starting in January 2016 until June 2016

In this position as a STERILITY ASSURANCE SPECIALIST you will create, review, correct and release documents to cover the reprocessing program. Additionally you will support and ensure sterility validations. Create internal validations protocols and reports will be including in your tasks.

YOU BRING TO THIS ROLE:

- Minimum of 5 years' experience in clinical reprocessing
- Good knowledge in APPLICABLE MEDICAL DEVICE DIRECTIVE (MDD)
- Strong experience working with ISO 13485, ISO 9001, ISO 14971
- Work experience in government regulations and industry guidelines for clinical reprocessing (EN ISO 15883, EN ISO17665, EN ISO 17664, RKI GUIDELINE, AAMI TIR)
- Experience with critical design features for clinical reprocessing and identification of design features
- Good MS OFFICE knowledge
- Fluent in ENGLISH and German will be an advantage

If you are a communicative, able to INTERACT WITH MANAGERS at all levels with ORGANIZATION SKILLS and currently looking for a challenging new position that applies to your experience, then we look forward to receive your application!

If you've any further questions on the role please call JULIE MACKERER to get further information.