QA Document Controller (Remote)

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:

1. You will be responsible for document control: generating, managing, updating, retrieving and following-up quality documents both internally, and generated by vendors.

2. Make sure that the CMO batch documentation are compliant to GXP standards, including the review of GMP documentation.

3. You will route new quality documents for review and approval through DocuSign, maintain training log, and maintain vendor files within the QMS.

4. You will assist with the Quality Specialist supporting the implementation of the Quality Management System (QMS), carrying out day to day activities such as CAPAs, deviations, change controls.

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:

1. Relevant degree in a relevant life sciences discipline

2. Proven industry experience working in a GxP environment - (GMP, GLP, GDP preferred)

3. 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 |