We are currently looking for a Senior QA Associate to join a growing biotechnology company based in Hertfordshire. As the Senior QA Associate you will be responsible for supporting the manufacturing and release of products under the QMS environment, support product and batch record reviews, investigations into non-compliance and CAPA Management.
Duties and Responsibilities
Maintain quality supporting documentation to facilitate GMP Production
Write and review quality SOP's and associated documentation for GMP production
Carry out investigations for deviations and non-conformances.
Support MHRA licensing
Release documents and labels to the manufacturing production teams
Review change controls records impacting products
Implement CAPAs to improve product quality
Education and Experience
We are looking to identify the following in your profile:
Degree or Masters in a relevant scientific discipline and a number of years of GMP industry experience within a biotech, biologics or similar organisation.
MHRA licensing experience is essential to your application
Previous industry experience using QMS including implementation and development.
To find out more about Real please visit
Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC(phone number removed) England and Wales
Software Quality Assurance (Sqa)
Corrective And Preventive Action (Capa)
Product Quality Assurance