Global CMC Regulatory Director in London

Global CMC Regulatory Director in London

London Full-Time 80000 - 100000 £ / year (est.) No working from home possible
Shionogi Europe

At a Glance

  • Tasks: Lead regulatory strategy and execution for product submissions across Europe and global markets.
  • Company: Shionogi Europe, a leader in global health innovation.
  • Benefits: Competitive salary, health benefits, and opportunities for impactful work.
  • Other info: Join a dynamic team dedicated to improving global health outcomes.
  • Why this job: Make a meaningful impact in global health while advancing your career.
  • Qualifications: Senior level experience in CMC regulatory affairs and knowledge of EU/EMA regulations.

The predicted salary is between 80000 - 100000 £ per year.

Shionogi Europe is seeking an Associate Director/Director for CMC Regulatory Affairs to lead and oversee regulatory strategy and execution for products. This pivotal role supports successful submissions across Europe and global markets.

The ideal candidate will have senior level experience in CMC regulatory affairs, knowledge of EU/EMA regulations, and a scientific background. Join us at Shionogi to make a meaningful impact in global health.

Global CMC Regulatory Director in London employer: Shionogi Europe

Shionogi Europe is an exceptional employer that fosters a collaborative and innovative work culture, where employees are empowered to make a meaningful impact in global health. With a strong commitment to professional development, we offer numerous growth opportunities and support for continuous learning, all while being located in a vibrant and dynamic environment that encourages creativity and teamwork.

Shionogi Europe

Contact Details:

Shionogi Europe Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Global CMC Regulatory Director in London

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Shionogi Europe. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.

Join Relevant Professional Bodies

Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Shionogi Europe.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Shionogi Europe. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.

Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Shionogi Europe is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Global CMC Regulatory Director in London

CMC Regulatory Affairs
Regulatory Strategy
EU/EMA Regulations
Scientific Background
Submission Management
Leadership Skills
Project Management

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.

Showcase Relevant Experience

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.

Be Ready for Regulatory Scenarios

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.