I am currently working with an exciting Pharmaceuticals CDMO based in Central Scotland.
We are looking for a QA Manager to join the team who, along with the Senior Manager, Quality, will be responsible for ensuring compliant GMP operations are continuously maintained across the site.
You will provide direct supervision of the QA team charged with the review and management of investigations including root cause, product impact and CAPA, GMP document review, batch manufacturing record review, and executing internal and external audit program.
Hold a Science related qualification, at degree level or equivalent
Wide breadth and depth of knowledge in regulatory requirements and GMP
Knowledge and experience of EU GMP and Quality Assurance
Experience in an aseptic manufacturing environment
Strong proven leadership, management and team working skillsIf this QA Manager role looks like it could be the next step in your Pharmaceuticals career, please get in touch ASAP!
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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
Corrective And Preventive Action (Capa)
Good Manufacturing Practices