Quality Leader

The Product Quality Strategy Director is accountable for setting, integrating, and governing end-to-end Product Quality Strategy for business-critical assets from Commit to Pivotal Readiness through initial commercial launch in major markets and critical lifecycle change activities. The role serves as the independent Quality representative and One Quality Voice across CMC, Quality, R&D, MSAT, Manufacturing, Regulatory Affairs, Site Quality, QC, supply functions, and strategic partners. Through enterprise matrix leadership, the role ensures product quality, patient impact, regulatory and inspection readiness, supply continuity, and product quality risk management are embedded in development, registration, launch, commercialization, and lifecycle decisions. Oversight continues where post-approval supply-chain changes, acquisitions, alliance products, or strategically critical portfolios require sustained senior quality leadership outside manufacturing-site operational ownership. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Develop, maintain, and integrate end-to-end Product Quality Strategy for assigned assets from pivotal readiness through launch and lifecycle management, ensuring Quality, Technical Development, Product Quality Risk, Compliance, Regulatory, patient, and supply considerations are embedded in asset strategy and governance decisions. Lead the Product Quality Team and influence GSC Technical, GSC Product Strategy, GRA CMC, R&D CMC, Quality, R&D, MSAT, Manufacturing, Site Quality, QC, supply functions, and strategic partners to align priorities, decisions, readiness plans, and accountable delivery. Represent Quality as the One Quality Voice at PSLT, CMC, product, and other senior governance forums, providing objective risk-based recommendations, resolving quality-position differences, and escalating unresolved issues through appropriate governance routes. Provide Quality leadership for pivotal, filing, launch, inspection, and post-approval readiness, including strategic input to control strategy, comparability strategy, regulatory submissions, health-authority responses, PAI preparation, and critical quality controls, as applicable. Be accountable for Product Quality elements within CMC matrix teams and for Quality review, approval, and execution oversight of Product Quality deliverables and milestone-readiness activities, as required. Drive proactive product quality risk detection, assessment, governance, escalation, mitigation, and acceptance, ensuring clear accountable owners, effective action plans, documented rationale, and timely senior-governance visibility. Coordinate matrix oversight of relevant QMS and lifecycle processes for assigned assets, including changes, deviations, CAPAs, complaints, product quality reviews, validation, post-approval changes, dossiers, regulatory submissions, and associated controls. Drive end-to-end Product Quality for commercial Vaccines or Medicines as a competitive advantage through proactive product, process, analytical, digital, and knowledge-management improvements that strengthen patient outcomes, compliance, supply continuity, and business performance. Serve as global subject matter expert for new product introduction and product quality lifecycle change management and, as applicable, Major Change Control Reviewer, PIRC member, and Quality point of contact for Alliance and Strategic Partners. Improve Product Quality Strategy processes, standards, governance frameworks, and organizational capability through lessons learned, coaching, knowledge sharing, reusable tools, and continuous improvement. Translate complex technical, quality, compliance, regulatory, patient, and supply risks into clear business recommendations and governance decisions. Monitor product quality signals, complaint trends, deviations, CAPAs, product quality reviews, stability, and lifecycle information to identify emerging risks and required action. Drive timely communication, escalation, decision documentation, ownership, and follow-through for quality, compliance, regulatory, and supply risks. Coach and develop colleagues through technical guidance, decision support, knowledge sharing, and contribution to the PQSL community of practice Why You? Basic Qualification Bachelor's degree Minimum 10 years of pharmaceutical-industry experience across Quality and/or Technical functions Experience in GMP Experience with product lifecycle management Experience with product quality risk management and new product introduction Experience with regulatory submissions and inspection readiness Matrix leadership experience Governance participation experience Preferred Qualification Master's degree. Experience in more than one Quality or Technical role is preferred. Deep understanding of GMP, pharmaceutical quality systems, Quality Assurance and/or Quality Control, product lifecycle management, and global regulatory expectations. Demonstrated enterprise leadership capability connecting quality decisions to patient impact, product strategy, supply continuity, regulatory outcomes, and business priorities. Proven matrix leadership and stakeholder-influence skills, including resolving conflict, creating One Quality Voice, and driving delivery without direct line authority. Strong product quality risk-management capability, scientific judgment, systems thinking, and ability to make or recommend decisions under uncertainty and ambiguity. Deep understanding of GMP, pharmaceutical quality systems, Quality Assurance and/or Quality Control, product lifecycle management, and global regulatory expectations. Demonstrated enterprise leadership capability connecting quality decisions to patient impact, product strategy, supply continuity, regulatory outcomes, and business priorities. Proven matrix leadership and stakeholder-influence skills, including resolving conflict, creating One Quality Voice, and driving delivery without direct line authority. Strong product quality risk-management capability, scientific judgment, systems thinking, and ability to make or recommend decisions under uncertainty and ambiguity. #LI-GSK Skills Assurance Framework, Data Integrity, Digital Fluency, GxP Regulations, Influencing Without Authority, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Quality Strategy, Risk Awareness, Technical Writing Italian Salary Range / Fascia retributiva in Italia: EUR 83,250 to EUR 138,750 Belgium Salary Range / Fourchette salariale - Belgique: EUR 115,500 to EUR 192,500 The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate's skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate's skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate's skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria. Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. GSK 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. If you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at #J-18808-Ljbffr