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Vice President Sterility Assurance
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GSK Supply chain teams play a critical role in delivering high‑quality medicines and vaccines by ensuring manufacturing processes are scalable, compliant and efficient. The Vice President, Sterility Assurance will shape and execute a global sterility strategy across Engineering, QA, Business Units and MSAT, driving standardisation, robust risk controls and inspection readiness. Key Responsibilities
Own and deploy sterility assurance strategy, standards and governance to ensure regulatory compliance. Lead cross‑functional alignment and risk mitigation across Engineering, QA and MSAT. Standardise contamination control strategy and embed it in the QMS. Oversee facility design and equipment reliability aligned with sterility assurance requirements. Lead cleaning validation, process control and supplier qualification as it relates to sterility assurance standards. Integrate QMS, manage deviations and maintain inspection readiness. Chair monthly governance forums and drive strategic decisions. Build capability through Communities of Practice. Strategic Objectives
Accountable for transformation of global sterility assurance standards across Engineering, MSAT and Quality and ensuring they are in use across all sites. Set vision for the future to proactively meet regulatory expectations. Accountable for program management for execution / implementation to global standards. Deliver Annex 1 compliance through standardized global policies. Implement KPI dashboards for contamination control and cleaning validation. Define clear project and governance frameworks to clarify roles and responsibilities between global and local teams. Drive continuous improvement and proactive inspection readiness. Lead the uplift in capability building and leadership development across functions. External network/advocacy with industry forums and regulators to keep pace with evolving regulatory expectations and emerging technology. Basic Qualifications
Bachelor’s degree in microbiology, life sciences, engineering, or related field, or equivalent experience. Significant experience in sterility assurance, microbiology, or quality in a regulated manufacturing environment. Proven leadership in cross‑functional roles including QA, Engineering, and MSAT. Strong knowledge of Annex 1, GMP, and global regulatory requirements. Experience in inspection readiness. Excellent communication, governance, and stakeholder management skills. Preferred Qualifications
Advanced degree in microbiology, pharmaceutical sciences, or engineering. This role can be based at one of our manufacturing sites in the US (East coast), Europe or UK. Closing date for applications: 28th November 2025 The US annual base salary for new hires in this position ranges from $225,000 to $375,000. The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share‑based long‑term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. GSK is an Equal Opportunity Employer. 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 require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1‑877‑694‑7547 (US Toll Free) or +1 801 567 5155 (outside US).
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