Job Description
Experience pharmaceutical company seeks Quality Assurance Specialist for contract position in Midlands. Key responsibilities include overseeing CAPA's, deviations, batch release review and change controls, as well as compliance and documentation. Ideal candidate will have experience in managing deviations, CAPA's and non-conformances in sterile manufacturing facilities, and familiarity with EM and environmental monitoring. Required skills include: • Experience in managing deviations, CAPA's and non-conformances in sterile manufacturing facilities • Experience in sterile product GMP manufacturing environment and familiarity with associated technologies and quality processes • Demonstrated experience in Risk Analysis, Investigation, Problem Solving • Experience in batch record review and process improvement • Experience in performance of audits • Proficiency with Microsoft Word, Excel, PowerPoint, Visio and ideally an electronic document system • Ability to interpret technical procedures, SOP's, GMP's and applicable regulations and provide advice and guidance as required Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative. By accepting this role, you agree to our Terms of Service and Privacy Statement, which govern your use of Morgan McKinley Services.