Quality Assurance Officer

SRG are working on several opportunities for QA Officers.If you have Quality Assurance (QA) experience from a GMP environment then we could have a great next step for you.The Role:Provide QA input to project activities including review and approval of change requests, specifications, Standard Operating Procedures, Manufacturing Procedures and Analytical Procedures.Participate in quality related investigations, assist in the development and approval of effective CAPA in order to resolve production, audit and customer issues.Identify and escalate any identified cGMP areas of concern.Participate in validation activities including approval of protocols and reports for analytical methods, manufacturing processes, analytical / production / packaging equipment and cleaning proceduresParticipate in the audits of suppliers, production and support functions as required.Be involved in the preparation for MHRA/FDA and other regulatory body audits.Review the relevant documentation relating to incoming raw materials and perform the disposition activities as required.Reviewing manufacturing, laboratory and associated documentation prior to performing the relevant disposition of final products. Where potential issues exist, these are to be highlighted to the QA manager.Requirements:Degree in a relevant scientific, engineering or business discipline and/or relevant industry experienceSeveral years’ experience within Quality Assurance working to GMP guidelinesExperience of working within a Quality Management System e.g. completing or reviewing QMS documentation (SOPs/Deviations /Investigations /CAPA)Experience of preparing and assisting in external audits with regulatory bodies such as FDA and MHRAOrganised and attention to detailStrong communication skills across all levels