Quality Assurance Associate Document Controller

Posted 15 January by Harris Lord Group

An exciting brand new opportunity has arisen to join a fast growing biotechnology company as a Quality Assurance Associate in Wales. You will have the opportunity to further develop and build on your quality experience in a cutting edge environment.

This opportunity gives you the chance to join a growing company who are at the forefront of their market.

The Company

An innovative biotechnology company who are going through impressive expansion, offering an excellent environment and growth for personal development. The site in Wales are carrying out innovative research targeting unmet medical needs.

The Role

This is a broad quality role within a small QA team with a particular focus on overseeing the QC data and documentation and ensuring compliance with the QMS. Another key aspect of the role will be to implement improvements within the Quality department and the wider QMS across the business.

Skills / Experience

v 1-2rs+ experience essential in a QA environment within pharmaceuticals/biologics

v Relevant scientific degree or equivalent

v Good understanding of GXP guidelines (GMP and GLP essential)

v Experience of data review will be an advantage

Key words

Quality, Assurance, QA, documentation, reviewing, batch, QMS, corrective, preventative, GLP, GMP, management, system, good, manufacturing, practice, laboratory, QC, control, SOPs, GxP

Harris Lord is acting as an employment agency.

Reference: 33643015

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