Description
A global pharmaceutical organisation require a QC Specialist (CMC) to assist in CMC documentation so that all manufactured products continuously comply with up-to-date regulatory requirements and are considered ``state-of-the art`` methods.Responsibilities to include:
* Write associated CMC analytical documents to support product registration.
* Positioning reports into correct CMC format.
Minimum requirements:
* Chemist with a significant experience in Quality Control
* Thorough knowledge of requirements and QC
* QC & Regulatory expertise in Pharmaceutical industry
* Exposure to CMC documents
* English: Fluent (oral & written)
This is a short term contract opportunity working in a dynamic environment offering competitive rates of pay. Please apply now for more information.