Quality Reviewer

Vor 6 Tagen


Stein, Schweiz Universal-Job Vollzeit

In this role, you are responsible for independent and timely execution of routine analyzes according to test specification of Medical Devices to GxP Standards. You document the analysis results in compliance with the associated GMP guidelines. Further, you control raw data and put them into the electronic system.

**Motivation**
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us

**Firmenprofil**
Successfully operating company within the pharmaceutical industry

**Spezielles**

**Erfahrung**
Technical understanding is an advantage.

**Ausbildung**
Working experience in Laboratory environment

**Sprachen**
German: Advanced
English: Intermediate

**Arbeitsort**
Stein

**Arbeitsbeginn**
Asap

**Vakanz-Nummer**
P-13-8054



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