Senior Regulatory Affairs Lead - UK/EU Submissions & CMC
Senior Regulatory Affairs Lead - UK/EU Submissions & CMC

Senior Regulatory Affairs Lead - UK/EU Submissions & CMC

Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead regulatory submissions and ensure compliance with UK/EU legislation.
  • Company: Dynamic pharmaceutical company based in Greater London.
  • Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
  • Why this job: Make a significant impact in the pharmaceutical industry while managing complex projects.
  • Qualifications: Degree in a scientific discipline and substantial regulatory experience required.
  • Other info: Work independently in a fast-paced environment with career advancement potential.

The predicted salary is between 48000 - 72000 £ per year.

A pharmaceutical company in Greater London is seeking a Principal Regulatory Affairs Officer. The role involves providing full regulatory input for the submission and assessment of Marketing Authorisation Applications, ensuring compliance with UK and EU legislation.

Candidates should have a degree in a scientific discipline and substantial regulatory experience across the product lifecycle. This position offers an opportunity to work independently while managing complex submissions and deadlines.

Senior Regulatory Affairs Lead - UK/EU Submissions & CMC employer: Select Pharma

Join a leading pharmaceutical company in Greater London that values innovation and compliance, offering a dynamic work culture where your expertise in regulatory affairs will be recognised and rewarded. With a strong commitment to employee development, you will have access to continuous training and growth opportunities, ensuring you stay at the forefront of industry advancements. Enjoy a collaborative environment that fosters teamwork and encourages independent thinking, making it an ideal place for professionals seeking meaningful and impactful careers.
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Contact Detail:

Select Pharma Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Regulatory Affairs Lead - UK/EU Submissions & CMC

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be when it comes to landing that dream job.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of UK and EU regulations. We recommend creating a cheat sheet of key legislation and recent changes. This will show your potential employer that you’re not just knowledgeable but also genuinely interested in the role.

✨Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. We all know that first impressions count, so let’s make sure you shine!

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage directly with us.

We think you need these skills to ace Senior Regulatory Affairs Lead - UK/EU Submissions & CMC

Regulatory Affairs Expertise
Marketing Authorisation Applications
UK Legislation Compliance
EU Legislation Compliance
Scientific Degree
Regulatory Experience
Product Lifecycle Knowledge
Project Management
Deadline Management
Independent Working

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your regulatory experience, especially in UK and EU submissions. We want to see how your background aligns with the role, so don’t be shy about showcasing your achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Senior Regulatory Affairs Lead position. We love seeing passion and clarity, so make it personal and engaging.

Showcase Your Scientific Knowledge: Since a degree in a scientific discipline is essential, ensure you mention your qualifications prominently. We’re looking for candidates who can demonstrate their understanding of the product lifecycle and regulatory frameworks.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!

How to prepare for a job interview at Select Pharma

✨Know Your Regulations

Make sure you brush up on the latest UK and EU regulations related to Marketing Authorisation Applications. Being able to discuss specific legislation and how it impacts submissions will show your expertise and readiness for the role.

✨Showcase Your Experience

Prepare to share detailed examples of your past regulatory experiences, especially those involving complex submissions. Highlight how you managed deadlines and ensured compliance throughout the product lifecycle, as this will demonstrate your capability to handle the responsibilities of the position.

✨Research the Company

Take some time to understand the pharmaceutical company’s portfolio and recent developments. Knowing their products and any recent news can help you tailor your answers and show genuine interest in their work during the interview.

✨Ask Insightful Questions

Prepare thoughtful questions about the team dynamics, challenges they face in regulatory affairs, and how success is measured in this role. This not only shows your enthusiasm but also helps you gauge if the company culture aligns with your values.

Senior Regulatory Affairs Lead - UK/EU Submissions & CMC
Select Pharma
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  • Senior Regulatory Affairs Lead - UK/EU Submissions & CMC

    Full-Time
    48000 - 72000 £ / year (est.)
  • S

    Select Pharma

    50-100
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