Senior Regulatory Affairs Associate

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About the role

About GSK   GSK is a global biopharma company with a special purpose: to unite science,   technology   and talent to get ahead of disease together. Our success absolutely depends on our people. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be, where they can continue to grow and look after their wellbeing.   If you share our ambition, join us at this exciting moment in our journey to get Ahead Together.   About the role   We are seeking a   Senior Regulatory Affairs Associate   to join our   Vaccines Regulatory Affairs team   based in our   Abbotsford office,   Melbourne .   Supporting a diverse vaccines portfolio across Australia and New Zealand,   you'll   work on new product registrations, new indications and lifecycle management activities while partnering with local and global stakeholders to help bring innovative vaccines to patients.   This role offers broad exposure across the product lifecycle, from supporting regulatory strategies for pipeline assets through to   maintaining   an established portfolio. With a strong pipeline and opportunities to work on future vaccine innovations, this is an excellent opportunity to further develop your regulatory career within a global organisation.   Your role will be varied and will include:   • Leading regulatory submissions for new products, new   indications   and lifecycle activities   • Managing designated products and acting as the local regulatory lead   • Developing regulatory strategies and responding to health authority questions   • Partnering with local and global stakeholders to deliver regulatory and business objectives   About you   We are looking for a collaborative and proactive regulatory professional who enjoys working across complex projects and building strong stakeholder relationships.   You will have a strong background in pharmaceutical Regulatory Affairs and a passion for supporting patient access to innovative medicines and vaccines. Experience in both new registrations and lifecycle management is highly   valued,   however we welcome   applications from professionals who are looking to broaden their experience across the full product lifecycle.   You will need:   • A science-based degree or postgraduate qualification in a relevant discipline   • At least 3 years' experience in Regulatory Affairs within the pharmaceutical industry   • Experience supporting new product registrations and/or lifecycle management activities   • Strong communication , stakeholder   management   and organisational skills     Why join us?   At GSK, we challenge ourselves to get Ahead Together, to make a positive impact on global health, drive innovation and create an environment where our people can thrive. Our culture inspires performance,   development   and growth.   By joining GSK,   you'll   enjoy:   • A flexible and life-friendly working approach, allowing you to do your best work   • Being part of a diverse organisation that reflects the communities we serve   • Development and progression opportunities on a global scale   • 5 Feel Good Days and 1 Volunteer Day each year   • The   option   to   purchase   up to 4 weeks'   additional   leave per year   • Access to discounted health insurance   • Certified Great Place   To   Work® May 2026-May 2027   * LI-GSK   Skills Digital Fluency, Pharmaceutical Regulatory Affairs, Problem Solving, Regulatory Affairs Management, Regulatory Strategies     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 suc

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