Manager - Submission Management

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your Role:

In this pivotal role, you will lead and shape the Submission Management sub-team within Global Regulatory Affairs, ensuring that every regulatory submission meets the highest standards of quality, compliance, and timeliness. You will be accountable for the day-to-day performance of your team — setting priorities, coaching team members, and driving continuous improvement across submission processes. As the primary expert for electronic Common Technical Document (eCTD) and submission management, you will guide your team through complex regulatory challenges, harmonize activities across functional areas, and serve as a key point of contact for submission-related expertise.

You will collaborate closely with cross-functional stakeholders to establish and monitor key performance indicators, support onboarding and capability development, and ensure the long-term sustainability of your team’s knowledge and capacity. Operating in a dynamic matrix environment, you will play a central role in streamlining regulatory operations and aligning submission activities with the broader strategic objectives of the organization.

Who You Are:

• You bring 9 to 11 years of professional experience in regulatory publishing and submission management within the pharmaceutical industry, with at least 2 years in a team leadership or supervisory capacity.