Beschreibung
Freelance - Regulatory Reviewer for Changes and Technical Files - SwitzerlandMy client an international top 10 company within the Medical Devices market currently seeks a Regulatory Reviewer for Changes and Technical Files to come on board for 11 months in fulltime.
Tasks:
As a Regulatory Reviewer for Changes and Technical Files will act as a reviewer of changes conducted for marketed Medical Devices in order to asses and document completeness of change assessment with focus on Regulatory aspects and identify and document deficiencies.You have to review technical files and content for completeness as well as interpreting of test data. Furthermore supporting of non clinical and clinical literature searches and interpretation will be one of your tasks.
Requirements:
You should be experienced within the Medical Devices industry especially with Regulatory, labelling, quality or engineering. Also the basic understanding of European Medical Devices Regulations is required. The ability to review and work according to checklist of requirements is necessary.
Furthermore you should be fluent in English AND German!
This project is your change to come onboard for 11 months at one of the global top ten companies within the Medical Devices market.
If you are looking for a challenging and varied freelance role in an international environment, a market-based compensation package and modern working conditions, you should apply immediately.
For more information, contact Marcus Müller at Real Pharma on or m.muller'at'realstaffing.com
Keywords: subject matter expert, regulatory reviewer, changes, technical files, fulltime, freelance, regulatory, review, reviewing, mechanical, shelf life, sterility, reprocessing, clinical,/on-clinical literature, medical devices
To find out more about Real please visit www.realstaffing.com