Regulatory Affairs Advisor

Contract

Full-time, Permanent.

Closing date

12th June 2026

Recruitment Partner

Katrina, katrina.wuk@boots.co.uk

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.

Find out more at http

//boots.jobs/rewards. Exclusions may apply; eligible roles only.

A bit about usAt 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.