Description
QA Associate 50% NOVJP (m/f)
Reference: -en
Start: 06/18
Duration: 7 MM++
Main tasks:
- Timely and compliant handling and approval of product returns
- Support QA Head on product release
- Ensure compliant archiving of GxP Documents
- Ensure trainings of the CH associates are completed on time
- Gather maintaining and report Key Quality Indicators in accordance with division quality requirements
- Is obligated to report any complaint (e.g., Adverse Event or Quality complaint) within 24h from the receipt to the Alcon Regulatory Affairs department in accordance to the valid local SOPs
Main qualifications
- BS degree in scientific discipline or equivalent experience in pharmaceutical environment
- Fluent in German and English
- Profound experience in a pharmaceutical environment, preferably in QA
- Experience in batch release
- Experience in medical devices requirement is a plus
Main advantages:
- Option to be extended
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.