At a Glance
- Tasks: Provide regulatory guidance and manage submissions for UK healthcare products.
- Company: Global healthcare company focused on innovation and compliance.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Join a dynamic team and make a difference in healthcare compliance.
- Qualifications: Degree in pharmacy or related field; experience with MHRA preferred.
- Other info: Collaborative environment with a focus on product development and regulatory excellence.
The predicted salary is between 36000 - 60000 £ per year.
A global healthcare company is seeking a Regulatory Affairs Specialist to provide regulatory guidance and support for UK marketed products.
Responsibilities include:
- Acting as a liaison with MHRA
- Managing regulatory submissions
- Collaborating with cross-functional teams
Ideal candidates will have a degree in pharmacy or a related field, and experience with MHRA and oncology is preferred. The role demands excellent communication skills and regulatory knowledge to ensure compliance and support product development.
Strategic Regulatory Lead – UK/MHRA Submissions & Compliance employer: Daiichi Sankyo Europe GmbH
Contact Detail:
Daiichi Sankyo Europe GmbH Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Strategic Regulatory Lead – UK/MHRA Submissions & Compliance
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field, especially those with experience in MHRA submissions. Use platforms like LinkedIn to connect and engage with them; you never know who might have a lead on your dream job!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK regulations and compliance. We recommend creating a cheat sheet of key points about MHRA processes and oncology regulations to impress your interviewers with your expertise.
✨Tip Number 3
Showcase your communication skills! During interviews, be ready to discuss how you've effectively collaborated with cross-functional teams in the past. We want to see how you can bridge gaps and ensure smooth regulatory submissions.
✨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 Strategic Regulatory Lead – UK/MHRA Submissions & Compliance
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with MHRA and oncology. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects or achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory affairs and how your skills can help us navigate the complexities of UK compliance. Keep it engaging and to the point.
Show Off Your Communication Skills: Since excellent communication is key for this role, make sure your application reflects that. Use clear, concise language and structure your documents well. We want to see that you can convey complex information effectively!
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. Plus, we love seeing applications come in through our own platform!
How to prepare for a job interview at Daiichi Sankyo Europe GmbH
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of UK regulations and the MHRA's processes. Familiarise yourself with recent changes in regulatory guidelines, especially those related to oncology products. This will show that you're not just a candidate but someone who is genuinely interested in the field.
✨Showcase Your Communication Skills
Since the role requires excellent communication, prepare examples of how you've effectively communicated complex regulatory information in the past. Think about times when you acted as a liaison between teams or stakeholders and be ready to discuss these experiences during the interview.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world regulatory scenarios. Practice articulating how you would handle specific challenges related to MHRA submissions or compliance issues. This will demonstrate your critical thinking and ability to navigate complex situations.
✨Collaborate and Connect
Highlight your experience working with cross-functional teams. Be prepared to discuss how you’ve collaborated with different departments to ensure compliance and support product development. This shows that you can work well in a team environment, which is crucial for this role.
