QA and Regulatory Consultant (Remediation)

Beschreibung

Rate: 120 – 140 CHF
Duration 6-8 months (ideally full-time: 40 hours / week)

This major top-10 Pharmaceutical / Devices Company works in developing innovative medical devices, biopharmaceutical medicines, vetinary products and orthopaedic products. This is a long-term contract (up to 8 months) and the main purpose of the role is performing remediation activities generated from the Management Review Legacy Reviews to ensure adequate product and process risk review.

Skills required:
? Expert knowledge of the FDA QSR and ISO 13485/ ISO 9001
? Able to review CAPA and sub-system data
? Expertise within GMPs
? Working knowledge of PAL
? Ability to build partnerships internally and externally
? Fluent in German and English
? Interview process: Telephone interview only

Urgent position

To apply, call or send your CV to Laura Brum, Recruitment Consultant – RA / QA