- Non-Laboratory & Other Scientific Roles
About this job
New opportunity for an experienced QA professional or aspiring QA Chemist to join a world-leading laboratory at an exciting time of expansion!
As a key member of the Quality Assurance team you will review QC data and certificates, stability protocols and reports as well as reviewing SOPs and method transfers. Additionally, as a QA Advisor you will be conducting inspections of manufacturing and laboratory areas and auditing batch records. A key aspect of your role will be to act as a contact for Quality Assurance GMP enquires and advise staff of the specific regulatory requirements as appropriate.
You will need:
- 12-months+ experience in QA
- Experience working to GMP and/or GLP regulations
- Understanding of deviations, OOS & CAPAs etc
- Knowledge of auditing is highly desirable
- Excellent communication skills and team player
QC Chemists with some experience in QA tasks i.e. reviewing and updating SOPs, reporting deviations, who are looking to move into QA are also invited apply. Full training provided.
Apply now to VRS!
Keywords: QA, Quality, Quality Assurance, Chemicals, Chemistry, Biopharmaceutical, GMP, Good Manufacturing Practice, cGMP, GLP, Good Laboratory Practice, Analyst, Chemist, QC, Quality Control, Stability, Audit, OOS, Deviations, CAPA, Northampton, Northamptonshire, Rushden, Wellingborough VRS6685HQ
Follow VRS Recruitment on LinkedIn to view all our latest vacancies!
Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website.