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- Tasks: Support regulatory strategies and product submissions for drug products.
- Company: Leading pharmaceutical recruitment consultancy with a focus on innovation.
- Benefits: Flexible hybrid working, competitive salary, and potential contract extension.
- Why this job: Join a dynamic team and make a difference in the pharmaceutical industry.
- Qualifications: Bachelor's degree in a scientific discipline and knowledge of UK/Ireland regulations.
- Other info: 12-month contract with opportunities for growth and development.
The predicted salary is between 36000 - 60000 £ per year.
A leading pharmaceutical recruitment consultancy is seeking a Regulatory Affairs Associate to support regulatory strategies and product submissions for drug products. The role offers a flexible hybrid working arrangement and involves working three days from home and two days in the office.
Candidates should possess a Bachelor's degree in a relevant scientific discipline and have experience with UK and Ireland regulatory labelling requirements. This is a 12-month contract with the opportunity for extension based on performance.
Senior Regulatory Affairs Specialist – UK & Ireland (Hybrid) employer: Quality Start
Contact Detail:
Quality Start Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Affairs Specialist – UK & Ireland (Hybrid)
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn. Join relevant groups and engage in discussions to get your name out there and learn about potential job openings.
✨Tip Number 2
Prepare for interviews by brushing up on UK and Ireland regulatory labelling requirements. We recommend creating a cheat sheet of key points to discuss, so you can showcase your expertise and impress the interviewers.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds and shows your enthusiasm.
✨Tip Number 4
Apply through our website for the best chance at landing that Senior Regulatory Affairs Specialist role. We make it easy for you to showcase your skills and experience directly to employers looking for talent like yours!
We think you need these skills to ace Senior Regulatory Affairs Specialist – UK & Ireland (Hybrid)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with UK and Ireland regulatory labelling requirements. 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 contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Scientific Knowledge: Since a Bachelor’s degree in a relevant scientific discipline is a must, make sure to mention your educational background clearly. We’re looking for candidates who can demonstrate their understanding of the pharmaceutical landscape.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about us!
How to prepare for a job interview at Quality Start
✨Know Your Regulations
Make sure you brush up on the UK and Ireland regulatory labelling requirements. Familiarise yourself with recent changes and how they impact drug products. This will show your potential employer that you're not just knowledgeable but also proactive in staying updated.
✨Showcase Your Experience
Prepare specific examples from your past roles where you've successfully navigated regulatory submissions. Highlight any challenges you faced and how you overcame them. This will demonstrate your problem-solving skills and experience in the field.
✨Ask Insightful Questions
Come prepared with questions about the company's regulatory strategies and how they approach product submissions. This shows your genuine interest in the role and helps you understand if the company’s values align with yours.
✨Emphasise Flexibility
Since this role offers a hybrid working arrangement, be ready to discuss how you manage your time and productivity while working from home. Share any tools or strategies you use to stay organised and effective in a flexible work environment.
