Quality Specialist

Slough, United Kingdom | Posted on 09/18/2026

We are looking for a Senior Process Quality Excellence Specialist who is collaborative, analytical, and quality-focused to joinour Global Clinical Sciences and Operations team, based in our Slough,UK offices.

About the role

You will help strengthen the quality framework that supports global clinical study operations with the role focusing on supporting the GCSOfunctions with audits and inspections. You are going to report to the Head of Process Quality Excellence and maintain the audit and inspection enabler withinthe GCSO Quality Management System.

Who you’ll work with

You will work within Global Clinical Sciences and Operations functional teams and collaborate across Global Quality, Regulatory Affairs,clinical teams, strategic partners, and other internal and external stakeholders. You are going to share guidance, build effective working relationships, and bring the right people together to prepare, participate and support the resolution of any audit and inspection findings and subsequentCAPA’s. You will represent GCSO in audit and inspection discussions and be the first point of contact for GCSO colleagues.

What you’ll do

• Leadand drive GCSO Inspection Readiness Activities across all GCSO functions working closely with the relevant inspection team(s), if applicable.
• Participate in Audit and Inspection planning with Global Quality.
• Actas audit host for GCSO Internal Audits, if applicable.
• Representor ensure GCSO representation including preparation during audits/inspections (on-site at UCB by internal and external parties) as applicable.
• SupportGCSO staff with audit/inspection responses, where required.
• Support Corrective and Preventive Action (CAPA) activity for internal (system) audits and findings from any audits and inspections where findings areraised to UCB in conjunction with department managers and subject matter experts. This includes CAPA tracking and monitoring for timely closure.

• Bachelor'sdegree or equivalent relevant experience in life sciences, quality,clinical research, or a related field.
• Atleast eight years of pharmaceutical experience, preferably in global quality assurance, clinical quality management, or clinical operations.
• In-depth knowledge of GCP, ICH guidelines, and relevant international and local regulations for clinical study operations.
• Hands-on experience supporting or leading global GCP audits, inspections,inspection readiness, responses, and CAPA activities.
• Atleast one years of experience writing and revising SOPs, with strong planning, investigation, and root-cause analysis skills.
• Clear written and spoken English, with the ability to explain complex topics and collaborate effectively across cultures, functions, and seniority levels.