Beschreibung
Freelance - Legacy Review Specialist - SwitzerlandI am currently taking care of more than 20 vacancies in an international Top 10 Medical Devices company inSwitzerland. At the moment I am seeking a Legacy Review Specialist for a five months project with a possible extension.
Responsibilities:
- Provide Audit reports as directed.
- Perform CAPA root cause and corrective / preventive action as necessary.
- Perform CAPA verification of effectiveness as necessary.
- Consultancy and guidance of all employees regarding maintenance, NCR, CAPA etc.
- Make recommendations to achieve compliance where shortfalls are found.
Requirements:
- Documented training in FDA QSR, ISO required.
- Thorough understanding of GMP and GCP guidelines.
- Must be proficient in the related ISO 13485 standards sections and related 21 CFR 820 regulatory subchapters.
-Ability to travel, to perform internal audits and be able to work independently.
-Fluently German and English spoken and written.
If a challenging and varied project in an international environment, a market-based compensation package and modern working conditions sounds like a good opportunity for you, please apply today!
If you are interested in this project or need further information please send your CV directly to Marcus Müller, You can also call me on
Keywords: Legacy Review, Medical Devices, CAPA, NCR, Audit, FDA QSR, ISO 13485, ISO 9001, GMP, GCP, 21CFR 820, German, English,Switzerland, freelance
To find out more about Real please visit www.realstaffing.com