Manager, CMC Vaccines Mature Projects, Regulatory Affairs

Site Name: USA - Maryland - Rockville, Hamilton Montana, USA - Pennsylvania - Upper Providence Posted Date: Jun 9 2026 At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting‑edge technology to transform people’s lives. GSK fosters a culture of ambition, accountability and integrity to accelerate assets that meet patients’ needs and have the highest probability of success. We unite science, technology and talent to get ahead of disease together. Position Summary You will lead Chemistry, Manufacturing and Controls (CMC) regulatory activities for mature vaccine projects. You will work with regulatory, development, quality, and manufacturing colleagues to ensure compliant submissions and supply continuity. We value clear communicators who are collaborative, pragmatic, and focused on patient impact. This role offers visible influence on the product lifecycle, professional growth, and the chance to help GSK unite science, technology and talent to get ahead of disease together. Responsibilities Lead CMC regulatory planning and execution for mature vaccine projects and lifecycle activities. Prepare, review and quality‑check CMC content for regulatory submissions, variations, and maintenance filings. Coordinate global dossier assembly, review cycles, and responses to regulatory questions. Advise cross‑functional teams on regional regulatory requirements and their impact on project timelines. Support supply continuity by ensuring regulatory requirements for manufacturing, release and distribution are in place. Contribute CMC subject matter expertise and share best practices to improve regulatory processes. Qualifications Basic Qualification Bachelor’s degree in pharmacy, chemistry, biotechnology or related scientific discipline, or equivalent experience. 2+ years’ experience in CMC regulatory affairs or pharmaceutical/biopharmaceutical development with direct involvement in regulatory submissions. Experience preparing or contributing to lifecycle submissions and post‑approval regulatory activities. Knowledge of CMC requirements for vaccines or biologics and of regulatory dossier formats. Prior experience working with cross‑functional teams including quality, manufacturing, and clinical development. Preferred Qualification Master's or PhD degree in a relevant scientific or regulatory field. Direct experience with vaccine development or biologics CMC regulatory strategy. Experience managing global submissions and interactions with major regulatory agencies. Experience supporting inspections and providing regulatory input for manufacturing or process changes. Familiarity with regulatory requirements across major regions such as the United States and European Union. Track record of driving process improvements or efficiencies in regulatory operations. Strong written and verbal communication skills with attention to detail. Salary and Benefits If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges from $113,850 to $189,750. The US salary ranges take into account factors including work location, candidate skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in a share‑based long‑term incentive program that depends on the level of the role. Available benefits include health care and other insurance benefits (for employees and families), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed for a specific country, relevant compensation will be discussed during the recruitment process. If you require an accommodation or other assistance to apply for this position, please contact us at View email address on click.appcast.io. Equal Opportunity Statement 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. #J-18808-Ljbffr GlaxoSmithKline