At a Glance
- Tasks: Lead regulatory strategy and execution for global development portfolios.
- Company: Shionogi Europe, a leader in pharmaceutical innovation.
- Benefits: Competitive salary, career advancement, and high visibility within global teams.
- Other info: Opportunity to drive submissions and engage with health authorities.
- Why this job: Shape regulatory strategy and collaborate with senior leadership on impactful projects.
- Qualifications: Senior CMC regulatory experience and strong communication skills.
The predicted salary is between 63000 - 77000 £ per year.
Shionogi Europe is seeking an Associate Director, CMC Regulatory Affairs to lead regulatory strategy and execution across development portfolios in the EU and beyond. This global role requires senior CMC regulatory experience and the ability to drive submissions, lifecycle management, and regulatory interactions with health authorities.
The role offers high visibility within global development teams, collaboration with senior leadership, and the opportunity to shape regulatory strategy.
Associate Director, Global CMC Regulatory Strategy employer: Shionogi Europe
At Shionogi, we pride ourselves on fostering a purpose-driven and agile work environment that empowers our employees to make a significant impact in global health. As an Associate Director/Director in CMC Regulatory Affairs, you will enjoy high visibility within global development teams, collaborate closely with senior leadership, and have the unique opportunity to influence regulatory strategies across diverse therapeutic areas. Our commitment to innovation and scientific excellence, combined with strong employee growth opportunities and a collaborative culture, makes Shionogi an exceptional employer for those seeking meaningful and rewarding careers in the pharmaceutical industry.
