Ph3Job Purpose /h3 pAs Director QBP, you will act as the trusted quality partner for assigned functions and third parties. You will give practical, clear quality advice and help teams reduce risk while improving how work gets done. You will shape quality strategies that enable reliable delivery, support quality investigations, and participate in inspection readiness activities. This role offers growth, real impact on how we work, and alignment with GSK’s mission. /p h3Your Responsibilities /h3 ul liProvides matrix management and leadership to cross-functional teams. /li liServes as the Quality Business Partner for assigned GSK RD functions, programs and/or Third Parties. Works closely with business to provide expert quality information, manage identified issues and support continuous improvement. /li liCollaborates with the Audit, Inspection, Risk and Issue Management team within RD Quality and Risk Management on all internal quality audits, regulatory agency inspections, risk assessments, issue and CAPA activities. /li liLeads inspection readiness activities and supports regulatory inspections. /li liSupports issues identification, reporting, root cause analysis and CAPA development. /li liEvaluates and/or reviews standard operating procedures and other activities in support of an integrated, cross‑functional QMS. /li liInfluences senior leaders to foster a commitment to quality and a culture of quality across GSK and GSK Third Parties. /li liResponsible for quality consultation for the assigned function. /li liDefines, implements and monitors the quality narrative/quality brief and reports any critical risk. /li liWorks with RD Data Analytics to define KPI, KQI and metrics needs for RD Quality and Risk Management and stakeholders. /li liShares key learning’s to drive simplification, continuous improvement and replicate best practices to drive quality into the business. /li liDefines the activities that need to be conducted to deliver the quality strategy for the assigned function, program and/or Third Party. /li liSupports due diligence and Merger Acquisition activities. /li liEnsures rapid communication of quality issues and risks including potential misconduct to appropriate leaders and colleagues. /li liSupports the investigations of potential serious breaches and critical issues. /li liLeads special assignments on various projects and workstreams as determined by RD Quality and Risk Management LT. /li /ul h3Additional Information /h3 ul liReporting line: Senior Director, Team Lead TA Quality /li liPeople management (direct/indirect reports, etc.): no /li liBusiness travel requirements: limited /li liPrimary location: GSK HQ /li liSecondary location: Wavre (Belgium), Upper Providence (US) /li liRelocation package provided: no /li liApplication closing date: Sunday, May 3rd 2026 EOD GMT /li /ul h3Basic Qualifications /h3 ul liBachelor’s degree in life sciences, pharmacy, engineering, or related discipline, or equivalent experience. /li liMinimum 5 years’ experience in quality, compliance, or regulatory roles within the life sciences industry. /li liExperience in drug development, regulatory compliance or quality management. /li liExperience in matrix management and leadership to cross-functional teams. /li liExpert knowledge and experience of GCP, GLP, GVP and regulatory requirements. /li liAbility to lead investigations, perform root cause analysis and deliver effective CAPAs. /li liStakeholder skills with experience influencing cross-functional teams and senior leaders. /li /ul h3Preferred Qualifications /h3 ul liAdvanced degree in a scientific or quality-related field or formal quality/compliance certification. /li liExperience implementing quality by design, risk-based quality management, and continuous improvement tools. /li liFamiliarity with regulated systems and quality metrics, including KPI/KQI development and reporting. /li liExperience working with regulated RD or manufacturing environments, including inspection readiness at pace. /li liComfort working in a matrix organization and leading through influence across multiple locations. /li liDigital awareness, including use of analytics or quality management systems to drive improvement. /li /ul h3Working pattern and location /h3 pThis role is based in the United Kingdom and offers a hybrid working arrangement. You will combine time in an office or site with remote working to balance collaboration and focused delivery. /p h3Equal Opportunity Employer /h3 pGSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. /p /p #J-18808-Ljbffr