At a Glance
- Tasks: Coordinate regulatory activities and manage submissions across the EU and UK.
- Company: Join MSD, a leader in making medicines accessible worldwide.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic role with a focus on collaboration and regulatory strategy.
- Why this job: Make a real difference in healthcare by ensuring access to vital medicines.
- Qualifications: Master's degree in pharmacy and 2 years of pharma industry experience required.
The predicted salary is between 45000 - 55000 € per year.
MSD is seeking a Regulatory Affairs Liaison based in London to support accessibility to medicines. The role involves coordinating regulatory activities across the EU, UK, Switzerland, and other regions while managing submissions and liaising with regulatory agencies.
Applicants should have a Master's degree in pharmacy or a related field, along with at least 2 years of experience in the pharmaceutical industry and a strong understanding of EU regulations. Fluency in English is required.
Regulatory Affairs Liaison — EU/UK Submissions & Strategy employer: MSD
MSD is an exceptional employer that fosters a collaborative and innovative work culture, dedicated to improving global health through accessible medicines. Based in the vibrant city of London, employees benefit from a dynamic environment that encourages professional growth and development, alongside competitive remuneration and comprehensive benefits. With a strong commitment to employee well-being and a focus on meaningful contributions to healthcare, MSD offers a rewarding career path for those passionate about making a difference.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Affairs Liaison — EU/UK Submissions & Strategy
✨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 in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on EU regulations and recent changes in the pharmaceutical landscape. We recommend practising common interview questions with a friend to boost your confidence and show off your expertise.
✨Tip Number 3
Tailor your approach! When you apply through our website, make sure to highlight your relevant experience in regulatory submissions and liaising with agencies. We want to see how you can contribute to making medicines accessible.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We believe it shows your enthusiasm and professionalism, which are key in the regulatory affairs world.
We think you need these skills to ace Regulatory Affairs Liaison — EU/UK Submissions & Strategy
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your relevant experience in regulatory affairs and showcases your understanding of EU regulations. We want to see how your background aligns with the role, so don’t be shy about emphasising your skills!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about supporting accessibility to medicines and how your experience makes you the perfect fit for this role. Keep it engaging and personal!
Showcase Your Experience:When detailing your experience, focus on specific projects or achievements that demonstrate your ability to manage submissions and liaise with regulatory agencies. We love seeing concrete examples of your work!
Apply Through Our Website:We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss any important updates from us!
How to prepare for a job interview at MSD
✨Know Your Regulations
Make sure you brush up on the latest EU and UK regulations related to pharmaceutical submissions. Being able to discuss specific regulations and how they impact the role will show that you're not just familiar with the basics, but that you’re genuinely engaged with the field.
✨Showcase Your Experience
Prepare to discuss your previous experience in regulatory affairs. Think of specific examples where you successfully managed submissions or liaised with regulatory agencies. This will help demonstrate your hands-on knowledge and problem-solving skills.
✨Research MSD
Take some time to understand MSD’s mission and values, especially their focus on accessibility to medicines. Being able to align your personal values with theirs during the interview can make a strong impression and show that you’re a good cultural fit.
✨Practice Your Communication Skills
Since the role involves liaising with various stakeholders, practice articulating complex regulatory concepts in simple terms. This will not only help you in the interview but also showcase your ability to communicate effectively in the role.
