At a Glance
- Tasks: Lead CMC regulatory strategy and oversee submissions for innovative medicines.
- Company: Shionogi, a purpose-driven company focused on global health innovation.
- Benefits: Empowering environment with high visibility and collaboration opportunities.
- Other info: Join a dynamic team and contribute to groundbreaking drug development.
- Why this job: Make a meaningful impact in healthcare while shaping regulatory strategies globally.
- Qualifications: Senior experience in CMC regulatory affairs and strong communication skills.
The predicted salary is between 70000 - 90000 £ per year.
Shaping Regulatory Strategy and Enabling Global Drug Development. At Shionogi, we are committed to improving global health through innovation, collaboration and scientific excellence. As our European development portfolio continues to grow, we are strengthening our regulatory capabilities to support successful product development and approvals across multiple therapeutic areas.
We are now seeking an Associate Director/Director, CMC Regulatory Affairs to lead strategic and operational regulatory activities across our development portfolio. This is a pivotal role with responsibility for defining CMC regulatory strategies, supporting global submissions and ensuring successful lifecycle management of products across the EU and beyond.
Why Join Shionogi? Shionogi offers a purpose-driven, agile environment where individuals are empowered to make a meaningful impact. This role provides high visibility across global development teams, close collaboration with senior leadership, and the opportunity to influence regulatory strategy across multiple programmes and markets.
About the Role: As Associate Director/Director, CMC Regulatory Affairs, you will lead and oversee CMC regulatory strategy and execution across assigned products and projects. This is a global role and therefore will allow the successful applicant to expand their knowledge from a core European focus. The role supports both projects in the development setting as well as lifecycle activities for approved products.
- Leading CMC regulatory strategy for development programmes and marketed products to support successful approvals
- Overseeing the preparation and review of CMC documentation for regulatory submissions, including CTAs, IMPDs, MAAs and lifecycle variations
- Advising cross-functional teams on CMC regulatory requirements, guidelines and agency expectations
- Supporting interactions with health authorities, including preparation for scientific advice and regulatory meetings
- Anticipating regulatory risks and ensuring mitigation strategies are in place to support business objectives
- Collaborating with global stakeholders across Europe, the US and Japan within multidisciplinary teams
- Contributing to regulatory process improvement initiatives and maintaining up-to-date regulatory intelligence
What Are We Looking For? We are looking for a Regulatory CMC scientist who can operate effectively in a complex and evolving global environment, balancing scientific, regulatory and business priorities.
You will bring:
- Senior level experience in CMC regulatory affairs within the pharmaceutical or biopharmaceutical industry
- Ideally having a scientific background from previously working in a quality control, formulation development or medicinal chemistry. Exposure to biologics would be adventitious
- Proven track record in developing and executing regulatory strategies across EU and global markets
- Strong experience in preparing and reviewing CMC documentation for regulatory submissions and lifecycle management
- In-depth knowledge of EU/EMA regulatory requirements and CMC/quality guidelines
- Ability to assess regulatory risk and develop mitigation strategies to support successful approvals
- Strong cross-functional collaboration, stakeholder engagement and influencing skills
- Excellent communication skills with the ability to operate effectively across global teams
Join Us: Join Shionogi and play a defining role in shaping regulatory strategy and enabling the successful development and approval of innovative medicines. If you are motivated by scientific excellence, global collaboration and making a meaningful impact in healthcare, we would welcome your application.
Associate Director/Director, CMC Regulatory Affairs in London 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 robust employee growth opportunities, makes Shionogi an exceptional employer for those seeking meaningful and rewarding careers in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director/Director, CMC Regulatory Affairs in London
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We think you need these skills to ace Associate Director/Director, CMC Regulatory Affairs in London
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Shionogi Europe!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Shionogi Europe that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Shionogi Europe!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Shionogi Europe, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Shionogi Europe
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Shionogi Europe that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Shionogi Europe’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
