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Document Management Specialist - England, United Kingdom - Hyper Recruitment Solutions
Description
We are currently looking for a QA Document Controller to join a leading Biotechnology company based in the North of the UK.
As the QA Document Controller you will be responsible for assisting in the development and on-going management of the companies Quality Management Systems.
Your duties as the QA Document Controller will be varied however the key duties and responsibilities are as follows:
Responsible for the development and implementation of the Quality Management System (QMS), carrying out day to day activities such as CAPAs, deviations, change controls and supplier qualification.
You will generate, retrieve, manage, and follow-up quality documents generated both internally and generated by vendors in the QMS.
To be successful in your application to this exciting opportunity as the QA Document Controller we are looking to identify the following on your profile and past history:
A working knowledge and practical experience with document / Quality Management Systems, and Electronic Document Management Systems
Key Words:
QA | Quality Assurance | QMS | Quality Management Systems | Clinical | GMP | GxP | Biotechnology | QDM | Quality Document Management Systems | Electronic Document Management Systems | Drug Discovery | CAPA | Deviations |