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 ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.

Are you ready to make a meaningful impact on global healthcare? As a Regulatory Manager, Delivery, CMC Small Molecules Mature Products you’ll lead a team responsible for delivering high-quality regulatory dossiers that ensure the continuity of supply for essential medicines. This role offers the chance to collaborate with diverse stakeholders, drive process improvements, and contribute to patient care worldwide. We value candidates who are proactive, detail-oriented, and passionate about leadership and regulatory excellence.

Key Responsibilities:

• Lead and develop a team to create a motivating and efficient work environment.
• Plan and ensure timely delivery of high-quality regulatory submissions for European and global markets.
• Act as a quality control point, ensuring submissions meet high standards and regulatory requirements.
• Identify risks to project timelines or quality, resolve issues, and escalate when necessary.
• Drive continuous process improvements to enhance efficiency and effectiveness.
• Build and maintain strong relationships with internal and external stakeholders.
• Monitor, analyze, and report team performance against departmental goals.