The role leads end-to-end planning and execution of regulatory deliverables to turn transformative science into approved medicines
Job Summary
The role leads end-to-end planning and execution of regulatory deliverables to turn transformative science into approved medicines.
Candidates will drive submission strategies, anticipate risks, and navigate complex procedures for small and large molecules across global regions.
The position requires building strong relationships with Health Authorities while coaching teams and contributing to continuous process improvement initiatives.
Matching Summary
The role leads end-to-end planning and execution of regulatory deliverables to turn transformative science into approved medicines.
Skills & Requirements
Must-have
Extensive regulatory experience in biopharma
Strong project management skills
Leadership of multi-disciplinary teams
Thorough knowledge of drug development
Expertise in Health Authority procedures
Nice-to-have
Managed first wave Marketing Application submissions
Knowledge of AZ Business processes
Experience with complex lifecycle management
Cultural awareness and influencing skills
Continuous improvement mindset
Key Requirements
Relevant University Degree in Science or related discipline
Extensive regulatory experience within the biopharmaceutical industry