INTERNATIONAL CMC REGULATORY AFFAIRS MANAGER

At AstraZeneca, we're not just about treating diseases - we're about defeating them.
We're on a mission to turn innovative science into life-changing medicines, and we need your help.
As a Reg Affairs Manager in our Oncology R&D department, you'll play a crucial role in gaining approval for our novel work on unmet medical needs.
If you're ready to make a real difference in the world of healthcare, we want to hear from you.
What you will do.
The role holders effectively manage the delivery, compilation and production of Chemistry, Manufacturing and Control (CMC) documentation for designated product ranges to deliver the needs for the international region and filings according to accelerated wave plans.
They project manage global CMC regulatory submissions ensuring that project activities and documentation are delivered to the required standards across the product Lifecyle.
The role holder will contribute and lead the regulatory CMC components of business-related projects.
They will have effective levels of interactive communication with stakeholders and project team members to ensure relevant timelines and regulatory commitments are communicated.
They will ensure the application of international CMC regulations and mentorship within AstraZeneca and lead/give to the development of new mentorship, policy, and processes.
Lead the timely preparation (may include authoring) and delivery of CMC contributions to the regulatory submissions linked to medicinal products throughout the lifecycle; including marketing authorisation applications and all post approval approval activities  Accountable for delivering “submission ready” international CMC modules to internal and external regulatory stakeholders in compliance with relevant AstraZeneca systems and procedures and ensuring submission quality.
Documenting maintenance and communication of Health Authority approval status.
Develops and builds expertise in regional regulatory requirements to ensure assurance of compliance of CMC submissions.
Project management expertise with the ability to adapt to changing situations to ensure on time delivery.
Ensure the learning from own projects are shared with other colleagues/within the functions.
Supporting the agreed strategy to employ fit for purpose content applying regulatory intelligence and to optimise proposed submission content Participation in regulatory execution and delivery meetings and communicate and provide relevant updates to the international CMC team.
Supply to business process optimisation activities to reduce waste and ensure efficiency.
Continually evolve and develop the regulatory expertise through proactive recording and communications of Health Authority interactions, responses and commitments.
Apply GxP principles according to the stage of product lifecycle.
Essential Skills/Experience.
Bachelor's degree in Science, Regulatory Sciences or Pharmacy Experience in Regulatory / Drug development (Industry or Health Authority) Breadth of knowledge of manufacturing, project, technical and regulatory management.
IT Skills Collaborator & Project management Professional capabilities.
Regulatory knowledge At AstraZeneca, we're not just a company - we're a community.
We're driven by a shared passion for science and success, and we believe in supporting each other every step of the way.
We're committed to fostering an inclusive, globally connected environment where everyone can thrive.
Here, you'll have the opportunity to work on groundbreaking projects, collaborate with industry-leading specialists, and develop your career in multiple roles and functions.
Ready to make your mark? Apply today and help us bring life-changing medicines to people around the world.
AstraZeneca embraces diversity and equality of opportunity.
We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.
We believe that the more inclusive we are, the better our work will be.
We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.
We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.