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- Tasks: Manage regulatory applications and ensure compliance with local regulations in a fast-paced environment.
- Company: Join a rapidly growing consultancy serving top multinational pharmaceutical companies.
- Benefits: Enjoy a part-time, fully remote role with flexible hours, outside IR35.
- Why this job: Be part of a dynamic team making a real impact in the pharmaceutical industry.
- Qualifications: Strong background in UK and Ireland regulatory affairs is essential.
- Other info: This is a 12-month contract offering a unique opportunity to work with leading clients.
The predicted salary is between 30000 - 42000 £ per year.
This rapidly growing Regulatory Affairs consultancy is looking for an experienced Regulatory Affairs Manager who specialises in UK and Ire registrations to fulfil a 12-month, remote contract which is outside IR35.
They count some of the biggest multinational pharmaceutical companies as clients and continue to provide regulatory solutions that drive success.
As Regulatory Affairs Manager UK and Ire you will be responsible for:
- Submitting regulatory applications to local Health Authorities
- Ensuring compliance with local regulations when updating the Summary of Product Characteristics (SmPC) and Patient Information Leaflet (PIL)
- Handling Health Authority queries post-submission
This is a fast-paced, busy team, and we are looking for someone with a strong UK and Ire Regulatory background who can hit the ground running.
This is a part-time contract job, 21 – 28 hours per week. It is fully remote and outside IR35.
For more information on this Regulatory Affairs Manager UK and Ire job please apply.
Regulatory Affairs Specialist UK and Ireland, Part time, outside IR35 employer: Hays
Contact Detail:
Hays Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Specialist UK and Ireland, Part time, outside IR35
✨Tip Number 1
Network with professionals in the regulatory affairs field, especially those who have experience with UK and Ireland regulations. Attend industry events or webinars to connect with potential colleagues and learn about the latest trends.
✨Tip Number 2
Familiarise yourself with the specific regulatory requirements for pharmaceutical products in the UK and Ireland. This knowledge will not only boost your confidence but also demonstrate your expertise during any discussions with the hiring team.
✨Tip Number 3
Prepare to discuss your previous experiences with regulatory submissions and compliance. Be ready to share specific examples of how you've successfully navigated challenges in this area, as it will show your capability to hit the ground running.
✨Tip Number 4
Research the consultancy's clients and their products. Understanding their portfolio will help you tailor your conversation and demonstrate your genuine interest in contributing to their success.
We think you need these skills to ace Regulatory Affairs Specialist UK and Ireland, Part time, outside IR35
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Regulatory Affairs Specialist. Familiarise yourself with UK and Ireland regulations, as well as the specific requirements for submitting regulatory applications.
Tailor Your CV: Highlight your relevant experience in regulatory affairs, particularly in the UK and Ireland. Emphasise any previous roles where you submitted applications to health authorities or updated product information.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for regulatory affairs and your understanding of the consultancy's needs. Mention your ability to work in a fast-paced environment and how your skills align with the job requirements.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is crucial in regulatory affairs.
How to prepare for a job interview at Hays
✨Know Your Regulations
Make sure you have a solid understanding of the UK and Ireland regulatory landscape. Brush up on the latest guidelines and be prepared to discuss how you've navigated these regulations in your previous roles.
✨Showcase Your Experience
Be ready to share specific examples of your past work in regulatory affairs, especially any successful submissions or compliance projects. Highlight your ability to handle Health Authority queries effectively.
✨Demonstrate Adaptability
This role is in a fast-paced environment, so emphasise your ability to adapt quickly. Share instances where you've had to adjust your approach or strategy to meet tight deadlines or changing regulations.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's clients and their regulatory challenges. This shows your genuine interest in the role and helps you understand how you can contribute to their success.
