Regulatory Affairs Advisor in Nottingham

Regulatory Affairs Advisor in Nottingham

Nottingham Full-Time 35000 - 45000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Provide regulatory guidance and support for Boots' medicinal products.
  • Company: Join Boots, a leading healthcare provider dedicated to community care.
  • Benefits: Generous discounts, retirement savings plan, and 24/7 counselling support.
  • Other info: Inclusive workplace with opportunities for growth and development.
  • Why this job: Make a real impact in healthcare while developing your career.
  • Qualifications: Life Sciences degree and regulatory experience in licensed medicines.

The predicted salary is between 35000 - 45000 £ per year.

Contract: Full-time, Permanent. Closing date: 12th June 2026.

Are you ready to make a difference? Join Boots as a Regulatory Affairs Advisor in Nottingham and be part of a team that is dedicated to delivering care, confidence, and connection in communities across the UK and Ireland. As Regulatory Advisor, you will be joining a team of experienced and best-in-class Regulators, delivering regulatory insights and controls to ensure the compliance of new and existing Boots Own brand products. You will report into the Regulatory Manager – Medicines and use your regulatory expertise, intelligence, and technical knowledge to maintain and deliver the licensed medicines portfolio for Boots. Stay at the forefront of changing regulations and work closely with a cross-functional team to develop compliant medicinal products that make a real impact.

Key responsibilities:

  • Provide regulatory guidance and support during new product development and maintenance activities.
  • Prepare, compile, and submit regulatory variations and manage associated documentation.
  • Maintain and update regulatory dossiers in line with EU/UK requirements.
  • Review and approve Product Information (including labelling and PILs) to ensure compliance with regulatory requirements.
  • Deliver post-approval activities within required timelines.
  • Manage regulatory change controls to ensure ongoing compliance.
  • Keep up to date with current legislation and guidelines, and share the knowledge with the team.

What you’ll need to have (our must-haves):

  • Life Sciences degree or equivalent qualification.
  • Demonstrated regulatory experience in licensed medicines (UK and EU) and ideally, exposure to additional product classifications, such as cosmetics or general products.
  • Experience in lifecycle management and maintenance of licensed medicine.
  • Relevant experience in regulatory affairs within the pharmaceutical or healthcare industry.
  • Strong understanding of EU/UK regulatory requirements.
  • Excellent communication and interpersonal skills.
  • Ability to work collaboratively in a team environment.
  • Strong attention to detail and organisational skills.

It would be great if you also have:

  • Experience working on NPD projects in complex borderline areas.
  • Experience working in own label supply/distribution.
  • A wider understanding of quality and pharmacovigilance or cosmetovigilance practices.

Where your brilliance can take you:

At Boots, we believe in your potential. With our commitment to your growth, you’ll have opportunities to develop your career further within our dynamic organisation.

Rewards designed for you:

  • Boots Retirement Savings Plan (up to 12% company contribution).
  • Generous employee discounts for you and a family member.
  • Enhanced maternity/paternity/adoption leave pay.
  • Access to free, 24/7 counselling and support through TELUS Health, our Employee Assistance Programme.

There’s lots more in our benefits and discounts, MyBoosts – there to give you that little lift in your everyday.

A bit about us:

At Boots, we're proud to be an equal opportunity employer, creating a place where everyone feels welcome, supported, and free to be themselves. We believe that when our people feel valued and included, they thrive, so we're committed to creating a brilliant Boots for our people so they can make a difference for our customers and colleagues every time.

What’s next?

If you apply, our team will be in touch to let you know the outcome of your application or to arrange next steps. Where a role is advertised as full-time, we are open to discussing part-time and job share options. If you require additional support as part of the application and interview process, we are happy to provide reasonable adjustments to help you be at your best.

We hope to hear from you soon. Be brilliant with Boots.

Regulatory Affairs Advisor in Nottingham employer: Boots

At Boots, we are committed to fostering a supportive and inclusive work environment where every employee can thrive. As a Regulatory Affairs Advisor in Nottingham, you will benefit from our extensive career development opportunities, competitive rewards including a generous retirement savings plan, and a culture that prioritises well-being through initiatives like our Employee Assistance Programme. Join us in making a meaningful impact in the healthcare sector while enjoying the perks of being part of a leading organisation dedicated to care and community.

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Contact Details:

Boots Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Regulatory Affairs Advisor in Nottingham

Tip Number 1

Network like a pro! Reach out to current or former employees at Boots on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.

Tip Number 2

Prepare for the interview by brushing up on your regulatory knowledge. Make sure you can discuss recent changes in EU/UK regulations and how they impact product compliance. Show us you’re on top of your game!

Tip Number 3

Practice your STAR technique for answering behavioural questions. Think of specific examples from your past experience that highlight your skills in regulatory affairs and teamwork. We want to see how you shine!

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining the Boots family.

We think you need these skills to ace Regulatory Affairs Advisor in Nottingham

Regulatory Expertise
Knowledge of EU/UK Regulatory Requirements
Regulatory Affairs Experience
Lifecycle Management
Documentation Management
Product Information Review
Attention to Detail

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the Regulatory Affairs Advisor role. Highlight your relevant experience in licensed medicines and any specific projects you've worked on that align with the job description. We want to see how your skills match what we're looking for!

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 you can contribute to Boots. Be sure to mention your understanding of EU/UK regulations and any unique experiences that set you apart from other candidates.

Showcase Your Team Spirit:Since collaboration is key in this role, make sure to highlight your teamwork skills in your application. Share examples of how you've worked effectively with cross-functional teams in the past. We love seeing candidates who can work well with others!

Apply Through Our Website:Don't forget to apply through our website! It’s the best way to ensure your application gets to us directly. Plus, it shows you're serious about joining our team at Boots. We can't wait to see your application!

How to prepare for a job interview at Boots

Know Your Regulations

Brush up on the latest EU/UK regulatory requirements related to licensed medicines. Being able to discuss recent changes or trends in regulations will show your expertise and commitment to staying informed.

Showcase Your Experience

Prepare specific examples from your past roles that highlight your regulatory experience, especially in lifecycle management and compliance. Use the STAR method (Situation, Task, Action, Result) to structure your responses effectively.

Communicate Clearly

Since excellent communication is key for this role, practice articulating complex regulatory concepts in simple terms. This will demonstrate your ability to work collaboratively with cross-functional teams and ensure everyone is on the same page.

Ask Insightful Questions

Prepare thoughtful questions about Boots' approach to regulatory affairs and product development. This shows your genuine interest in the role and helps you assess if the company culture aligns with your values.