Quality Assurance Specialist

SRG are working with a global name in the pharmaceutical industry to help them find a QA Specialist to join their team.If you have Quality Assurance (QA) experience from a GMP environment then this could be a great next step for you.The company offer an excellent benefits package and scope for growth and development. This role is for an initial 12 months with a strong likelihood of being extended from there.The Role:Perform batch reviews within required timelinesAuthor and review SOPsDocument and report all work in adherence with GMP and departmental proceduresReview change controls and provide feedback / corrections to authors and escalate concerns to the Quality Manager/Head of Quality where necessaryRaise, approve and review CAPAsRepresent the QA team for improvement projects and with clients and internal teamsAssist in the performance of supplier audits, supporting the Lead AuditorActs as a support to client and regulatory audits, helping with technical support to the audit team and responding to requests for documentation and informationConducts self-inspections / audits to ensure compliance with Quality Management System procedures and GMP regulationsEnsuring that a timely and effective communication and escalation of quality issues to the appropriate levels of managementCarries out site internal audits and identifies areas of GMP improvement during their daily dutiesCarries out training for QMS activities as defined by line managementRequirements: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

Created: 2026-02-02