Senior Director, Quality Operations Vaccines

Senior Director, Quality Operations VaccinesThe posting period will end on the 15th of February ****.The role can be done from any location that is close to a GSK location.Business IntroductionWe manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance.Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in **** to help make a positive impact on the health of millions of people.Our supply chain is vital to bringing our innovations to patients as quickly, efficiently and effectively as possible.Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.Position SummaryYou will own operational quality, regulatory readiness and supply continuity across all GSK Vaccines manufacturing sites.You will work closely with leaders in Quality, Supply, R&D and Regulatory to solve issues and deliver practical improvements.This role offers visible impact, and the chance to unite science, technology and talent to get ahead of disease together.Key ResponsibilitiesLead operational quality across all GSK vaccines manufacturing sites to ensure supply continuity and patient safetySet site-level quality priorities, metrics and governance with clear owners and deadlinesOversee investigations, root cause analysis and robust corrective and preventive actionsDeliver simplification and continuous improvement projects that improve quality, speed and costGrow capability through coaching, succession planning and inclusive leadership of quality teamsPartner with cross-functional teams to support inspections, transfers and new investmentsTranslate global and regional quality strategy into clear operational plans for Belgium sitesRun quality governance meetings and provide timely, transparent updates to senior stakeholdersEnsure compliance with good manufacturing practice, data integrity expectations and local lawsMonitor quality performance and act decisively to close gaps and mitigate risks to supplyProvide oversight for commissioning, qualification and transfer activities at sites and partnersPromote digital and data-led improvements to make quality processes simpler and more reliableBasic QualificationsBachelor's degree in scientific, engineering or related discipline, or equivalent experienceMinimum 10 years' experience in quality, manufacturing or regulatory roles in a regulated pharma environmentProven operational quality leadership in vaccines, biologics, sterile or complex manufacturingStrong experience with investigations, risk-based governance and CAPA managementDemonstrated track record of leading change and continuous improvement across teams or sitesPreferred QualificationsAdvanced degree such as MSc, MBA or PhD in a relevant fieldPractical experience with regulatory inspections and interactions with health authoritiesStrong people leadership in a matrix organisation with coaching and development experienceExperience with digital quality systems, automation and data integrity initiativesFamiliarity with sterility assurance, validation and complex supply networksProven success in delivering measurable quality performance improvementsBenefitsBenefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, paid caregiver/parental and medical leave.The position offers an annual bonus and eligibility to participate in a share-based long-term incentive program.#J-*****-Ljbffr